EXERCISE, ACTIVITY AND BETTER SLEEP IN MIDLIFE WOMEN: THE SWAN SLEEP STUDY

http://dx.doi.org/10.5665/sleep.2946

Consistently High Sports/Exercise Activity Is Associated with Better Sleep

Quality, Continuity and Depth in Midlife Women: The SWAN Sleep Study

Christopher E. Kline, PhD1; Leah A. Irish, PhD1; Robert T. Krafty, PhD2; Barbara Sternfeld, PhD3; Howard M. Kravitz, DO, MPH4,5; Daniel J. Buysse, MD1;
Joyce T. Bromberger, PhD1,6; Sheila A. Dugan, MD5,7; Martica H. Hall, PhD1
1
Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA; 2Department of Statistics, University of Pittsburgh, Pittsburgh,
PA; 3Division of Research, Kaiser Permanente, Oakland CA; 4Department of Psychiatry, Rush University Medical Center, Chicago, IL; 5Department of
Preventive Medicine, Rush University Medical Center, Chicago, IL; 6Department of Epidemiology, University of Pittsburgh, Pittsburgh, PA; 7Department
of Physical Medicine and Rehabilitation, Rush University Medical Center, Chicago, IL

Study Objectives: To examine relationships between different physical activity (PA) domains and sleep, and the influence of consistent PA on
sleep, in midlife women.
Design: Cross-sectional.
Setting: Community-based.
Participants: 339 women in the Study of Womens Health Across the Nation Sleep Study (52.1 2.1 y).
Interventions: None.
Measurements and Results: Sleep was examined using questionnaires, diaries and in-home polysomnography (PSG). PA was assessed in
three domains (Active Living, Household/Caregiving, Sports/Exercise) using the Kaiser Physical Activity Survey (KPAS) up to 4 times over 6
years preceding the sleep assessments. The association between recent PA and sleep was evaluated using KPAS scores immediately preceding
the sleep assessments. The association between the historical PA pattern and sleep was examined by categorizing PA in each KPAS domain
according to its pattern over the 6 years preceding sleep assessments (consistently low, inconsistent/consistently moderate, or consistently high).
Greater recent Sports/Exercise activity was associated with better sleep quality (diary restedness [P < 0.01]), greater sleep continuity (diary sleep
efficiency [SE; P = 0.02]) and depth (higher NREM delta electroencephalographic [EEG] power [P = 0.04], lower NREM beta EEG power [P < 0.05]),
and lower odds of insomnia diagnosis (P < 0.05). Consistently high Sports/Exercise activity was also associated with better Pittsburgh Sleep Quality
Index scores (P = 0.02) and higher PSG-assessed SE (P < 0.01). Few associations between sleep and Active Living or Household/Caregiving
activity (either recent or historical pattern) were noted.
Conclusion: Consistently high levels of recreational physical activity, but not lifestyle- or household-related activity, are associated with better sleep
in midlife women. Increasing recreational physical activity early in midlife may protect against sleep disturbance in this population.
Keywords: Physical activity, exercise, sleep, polysomnography, sleep depth, sleep continuity
Citation: Kline CE; Irish LA; Krafty RT; Sternfeld B; Kravitz HM; Buysse DJ; Bromberger JT; Dugan SA; Hall MH. Consistently high sports/exercise
activity is associated with better sleep quality, continuity and depth in midlife women: the SWAN Sleep Study. SLEEP 2013;36(9):1279-1288.

INTRODUCTION
Sleep disturbance affects 30% to 60% of midlife women1,2
and has significant consequences on health and functioning. In
addition to impaired daytime function,3 disturbed sleep is associated with a host of adverse health outcomes, including cardiometabolic morbidity.4,5 Among midlife women in particular,
sleep disturbance has been linked to increased risk of diabetes,6
the metabolic syndrome,7,8 and cardiovascular mortality.9
Unfortunately, very little is known about behavioral or lifestyle factors which could protect against sleep disturbance
during midlife. Physical activity may be one such protective
factor, but the current evidence is mixed. In the general population, physical activity is commonly associated with better
sleep,10 and exercise interventions have significantly reduced
the severity of various sleep disorders (e.g., insomnia, obstructive sleep apnea, periodic limb movements during sleep).11-13

However, this relationship is much less clear in midlife women.

Although higher levels of physical activity have been associated with less sleep disturbance in some studies of this population,2,14 others have found no relation.15-18
Methodological limitations likely contributed to the equivocal
state of knowledge regarding the relevance of physical activity to
sleep in midlife women. Sleep outcomes have often been based
on single-item measures14,17,18 or brief questionnaires focused on
insomnia-related symptoms2,15,16; objective measures of sleep
have not been assessed. This is especially relevant for midlife
women, since subjective reports and objective measures of sleep
are often divergent.19,20 In addition, the epidemiologic literature is
based on measurement of physical activity at a single time-point.
However, since the effects of relatively acute physical activity
on sleep may differ from those conferred by long-term patterns
of physical activity participation,21 multiple assessments over
time may yield a more accurate view of the sleep-related benefits
of habitual physical activity. Finally, studies have focused on
recreational physical activity, which fails to capture the overall
physical activity profile of midlife women.22,23 Compared to men,
women are less active in recreational physical activity, but similarly active when physical activity related to household and caregiving duties are considered.24
The purpose of this study was to examine the relationship
between physical activity and subjective and objective indices

Submitted for publication September, 2012

Submitted in final revised form January, 2013
Accepted for publication February, 2013
Address correspondence to: Martica H. Hall, Department of Psychiatry,
University of Pittsburgh School of Medicine, 3811 OHara Street, Room
E-1131, Pittsburgh, PA 15213; Tel: (412) 246-6416; Fax: (412) 246-5300;
E-mail: [email protected]
SLEEP, Vol. 36, No. 9, 2013

1279

Physical Activity and Sleep in Midlife WomenKline et al

of sleep in midlife women. Our primary interest was to examine

the relationship between sleep and two different timeframes
of physical activity, proximal (i.e., measured closest to sleep
assessments) and historical (i.e., pattern of activity over 5-6
years leading up to sleep assessments). We also sought to evaluate the relationship between sleep and different domains of
physical activity (i.e., lifestyle, household, recreational).

participants were not employed for pay outside of the home.

Domain-specific activity indices were calculated from mostly
ordinal Likert scale categorical responses, with higher scores
indicating greater activity in that specific domain (range: 1-5).
The KPAS has been validated against activity logs, accelerometers, and maximal oxygen consumption,22 with 1-month testretest reliability of 0.81 to 0.84 (varying by domain).22
Participants were excluded from analysis if KPAS data from
SWAN annual visits 5 and 6 were not available (n = 13). The 3
KPAS domains were evaluated for their association with sleep
in 2 ways: according to (1) recent physical activity and (2) the
historical pattern of physical activity. For analyses focusing
on recent physical activity, continuous KPAS scores from the
SWAN annual visit that preceded the SWAN Sleep Study were
used (1.05 0.70 years preceding SWAN Sleep). For analyses
examining the historical pattern of physical activity, participant
physical activity in each domain was classified as consistently high, inconsistent/moderate, or consistently low
based upon 2-4 KPAS assessments in the 5-6 years prior to the
SWAN Sleep Study. For classification in consistently high or
consistently low groups, KPAS domain scores needed to be
in the top or bottom tertile, respectively, at > 50% of the available time-points. Patterns of KPAS data that failed to meet this
criterion were classified as inconsistent/moderate activity for
that specific domain.

METHODS
Data for these analyses were from the Study of Womens
Health Across the Nation (SWAN) Sleep Study, a cross-sectional
study of sleep in a multi-ethnic sample of midlife women. The
SWAN Sleep Study is an ancillary study of the longitudinal
SWAN cohort (N = 3,302), a study of the menopausal transition and its consequences on health and functioning, being
conducted at 7 clinical sites across the United States.25 Data
for the SWAN Sleep Study were collected at 4 sites from 2003
through 2005: Chicago, IL; Detroit area, MI; Oakland, CA;
and Pittsburgh, PA. Each site recruited Caucasian participants,
while African American participants were recruited from the
Chicago, Detroit, and Pittsburgh sites, and Chinese participants
were recruited from the Oakland site.
Participants
A cohort of 370 SWAN Sleep Study participants was
recruited from the core SWAN study at the time of their fifth,
sixth, or seventh annual assessment. SWAN Sleep Study exclusion criteria were hysterectomy or bilateral oophorectomy,
current cancer treatment, current oral corticosteroid use, regular
nocturnal shiftwork, regular consumption of > 4 alcoholic beverages per day, or noncompliance with core SWAN procedures
(> 50% of annual visits missed, refusal of annual visit blood
draws). Written informed consent was obtained by all participants in accordance with approved protocols and guidelines of
the institutional review board of each participating institution.
Due to missing physical activity data (see below; n = 13) or
missing covariate data (n = 18), 339 women were included in
analyses. Compared to women whose data were retained for
analysis, excluded participants had significantly higher Pittsburgh Sleep Quality Index scores (mean standard deviation
[SD]: 7.40 3.46 vs. 5.57 3.05; P = 0.002) and lower relative beta electroencephalographic (EEG) power during NREM
sleep (1.41 0.52 vs. 1.83 1.03; P = 0.03). No other differences in sleep outcomes were observed. Excluded participants
did not differ from women retained for analysis on physical
activity (for participants missing covariate data) or covariates
(for participants missing physical activity data).

Sleep Assessment
The SWAN Sleep Study was conducted across a complete
menstrual cycle or 35 days, whichever was shorter. In participants with regular menstrual cycles, the protocol was initiated
within 7 days of the start of menstrual bleeding. Women who
had irregular menstrual cycles or were non-cycling were scheduled at their convenience.
A multi-modal assessment of sleep was conducted, employing
in-home polysomnography (PSG), daily sleep diaries, and validated questionnaires. This approach provided a comprehensive
assessment of sleep quality and indices of sleep duration, continuity and depth, as well as measurement of clinically significant sleep disturbance (e.g., sleep disordered breathing). Due
to differing amounts of data loss across sleep measures, the
sample size used for each respective sleep measure varied and
is indicated in parentheses below.
Polysomnography

Polysomnography (Vitaport-3; Temec Instruments, Kerkrade,

Netherlands) was conducted in participants homes according to
their habitual sleep and wake times over 3 consecutive nights at
the beginning of the Sleep Study protocol. The PSG montage
included EEG recorded at C3 and C4 referenced to linked
mastoids, bilateral electrooculogram, submentalis electromyogram (EMG), and electrocardiogram. Additional signals were
collected on the first night of PSG recording to assess sleep
disordered breathing (SDB) and periodic limb movements
during sleep (PLMS). For SDB assessment, additional signals
included nasal pressure cannula, oronasal thermistor, respiratory
inductance plethysmography, and fingertip oximetry, whereas
PLMS was monitored with bilateral anterior tibialis EMG.
Visual sleep stage scoring was conducted in 20-sec epochs
using standard sleep stage scoring criteria.27 In addition, SDB

Physical Activity Measurement

Physical activity was assessed with a modified version of the
Kaiser Physical Activity Survey (KPAS)22 at SWAN study entry
and at annual visits 3, 5, and 6. Adapted from the Baecke physical activity questionnaire,26 the KPAS assesses activity levels
during the previous 12 months in 3 distinct domains: Active
Living (e.g., frequency of television viewing [reverse scored],
active transportation such as walking to work), Household/
Caregiving (e.g., housework, childcare), and Sports/Exercise
(e.g., participation in recreational activity or sports). A fourth
domain, occupation, was not evaluated because many SWAN
SLEEP, Vol. 36, No. 9, 2013

1280

Physical Activity and Sleep in Midlife WomenKline et al

and sleep. Age was calculated at the time of the sleep study.
Race/ethnicity (Caucasian, African American, Chinese) was
defined by self-identification. Marital status, employment
status, and body mass index (BMI) were assessed at the closest
core SWAN visit prior to the sleep study. Marital status was
dichotomized as being unmarried (i.e., single, divorced, separated, widowed) or married/living as married, employment
status was dichotomized as not employed/employed for pay <
20 h/week or employed for pay 20 h/week, and BMI was
expressed as weight in kilograms divided by height in meters
squared. Educational attainment was assessed by self-report
during the core SWAN baseline interview and dichotomized
as less than a college degree or at least a college degree. Use
of medication that affects sleep was assessed over the course
of the study protocol, including both prescription and overthe-counter medicines. Medications were coded according to
the World Health Organization ATC classification system, and
medications with the following ATC codes were considered
to affect sleep: N02A (opioids), N03A (antiepileptics), N05B
(anxiolytics), N05C (hypnotics and sedatives), N06A (antidepressants), and R06A (antihistamines).33 Medication use was
dichotomized as none/infrequent (< 3 nights/week) or frequent
( 3 nights/week). Menopausal status was determined by
bleeding patterns reported during the closest core SWAN visit
prior to the SWAN Sleep Study: participants were categorized
as being pre- or early perimenopausal, late perimenopausal, or
postmenopausal, as previously described.34 Vasomotor symptoms (VMS) were assessed by daily diary entries. Each morning,
participants were asked to report the number of cold sweats, hot
flashes, and night sweats they experienced during the previous
nights sleep. Vasomotor symptoms were categorized as being
present if at least one VMS was reported that night, and participants were categorized based upon the frequency of nighttime
VMS: none to infrequent (< 25% of nights), intermittent (25
to < 75% of nights), and frequent ( 75% of nights). Smoking
status, caffeine consumption, and alcohol use were assessed
by daily diary entries. Smoking status was dichotomized as
none versus any reported smoking, caffeine consumption was
calculated as the mean daily number of caffeinated beverages, and alcohol use was calculated as the mean daily number
of alcoholic drinks.

events were evaluated using American Academy of Sleep

Medicine definitions,28 and PLMS was assessed using standard
rules.29 As measured from the first night of PSG recording,
the apnea-hypopnea index ([AHI] n = 321) and periodic limb
movement arousal index ([PLMAI] n = 323) were retained as
measures of SDB and PLMS, respectively. All other summary
sleep variables (n = 335) were averaged across the non-SDB/
PLMS assessment nights due to the potentially disruptive
effects of breathing and limb movement assessment on sleep.
Two summary measures, total sleep time (TST) and sleep efficiency (SE), were used in analyses. As a measure of sleep duration, TST was calculated as the total minutes of any sleep stage
following sleep onset. As a measure of sleep continuity, SE was
calculated as the ratio of TST to time in bed multiplied by 100.
As a measure of sleep depth, spectral analysis of the EEG
signal was performed to quantify power in the delta (0.5-4.0
Hz) and beta (16-32 Hz) frequency bands during NREM sleep
(n = 313). Modified periodograms were computed using the
Fast Fourier transform of non-overlapping 4-sec epochs of
the sleep EEG. Following automated artifact rejection,30 EEG
spectra were obtained for each artifact-free 4-sec epoch and
aligned with 20-sec visually scored sleep stage data. Relative
power (i.e., spectral power within a specific frequency band
[microvolts2/Hz] divided by the total power across 0.5 to 32
Hz [microvolts2/Hz], resulting in unit-less values) was used in
analyses to account for individual differences in EEG power.
Daily Sleep Diary

Subjective perceptions of sleep were obtained across the

entire Sleep Study protocol through daily completion of a
sleep diary. Each morning, participants were asked to recall the
prior nights sleep and indicate the time they got into bed and
attempted to sleep, how long it took to fall asleep, the final outof-bed time, and length of overnight awakenings. In addition,
participants were asked to indicate how rested they felt upon
awakening, from 0 (not at all) to 4 (extremely). Diary variables
retained for analysis included TST (as a measure of sleep duration), SE (as a measure of sleep continuity), and restedness (as
a measure of sleep quality), averaged across all valid nights
(mean [SD] nights per participant: 29.94 6.57; n = 339).
Questionnaires

Statistical Analyses
Prior to analyses, skewed sleep variables were transformed
(see Table legends for specific transformations employed).
Relationships between KPAS domain scores preceding the
Sleep Study were evaluated with Pearson correlations. To
evaluate associations between the patterns of different KPAS
domains in the 5-6 years preceding the Sleep Study, the likelihood of having a pattern of consistently high activity in
each domain relative to other domains was evaluated with
binary logistic regression.
To evaluate the relationship between sleep and recent physical activity (i.e., assessed at the SWAN visit immediately
preceding the Sleep Study), linear and logistic regression analyses were conducted for each KPAS domain (Active Living,
Household/Caregiving, Sports/Exercise). Multiple linear
regression analyses were conducted to examine each KPAS
domain score as a predictor of continuous sleep outcomes after

The 18-item Pittsburgh Sleep Quality Index (PSQI)31 was

administered on the fourth and last days of the Sleep Study
protocol (n = 336). The PSQI provides a validated measure
of sleep quality; scores range from 0-21, with higher scores
indicating worse sleep quality. PSQI scores were highly correlated (r = 0.81, P < 0.001) and were averaged for analyses. The
13-item Insomnia Symptom Questionnaire (ISQ)32 was administered on the last day of the Sleep Study protocol to provide
case definitions of insomnia (n = 331). The ISQ assesses the
frequency and severity of insomnia-related symptoms and
provides a dichotomous assessment of insomnia presence/
absence based upon DSM-IV criteria.
Covariates
Covariates were chosen for inclusion in statistical analyses
due to their established relationships with sleep and/or relevance to the possible relationship between physical activity
SLEEP, Vol. 36, No. 9, 2013

1281

Physical Activity and Sleep in Midlife WomenKline et al

were conducted for each KPAS domain. With adjustment for

previously noted covariates, ANCOVA evaluated differences
in continuous sleep outcomes between historical patterns of
each KPAS domain, with Tukey group comparisons performed
when appropriate. Binary logistic regression evaluated the odds
of having clinically significant sleep disturbance (as described
above) according to physical activity history pattern. Consistently low physical activity was used as the referent group.
Analyses were conducted using SAS v. 9.2 (SAS Institute;
Cary, NC). All statistical tests were 2-tailed, with statistical
significance set at P 0.05.

Table 1SWAN Sleep Study participant characteristics (N = 339)

Age, years
Body mass index, kg/m

52.2 (2.2)
2

30.0 (7.8)

Race/ethnicity, n (%)
Caucasian
African American
Chinese

161 (47.5)
120 (35.4)
58 (17.1)

Marital status, n (%)

Currently unmarried
Married/living as married

122 (36.0)
217 (64.0)

Education, n (%)
Less than a college degree
College degree or more

167 (49.3)
172 (50.7)

Employment status, n (%)

Not employed/employed < 20 h/week
Employed 20 h/week

77 (22.7)
262 (77.3)

Use of medication that affects sleep, n (%)

No/intermittent use
At least 3 nights/week

254 (75.5)
85 (24.5)

Menopausal status, n (%)

Pre-/Early perimenopause
Late perimenopause
Postmenopause/surgical

208 (61.4)
69 (20.4)
62 (18.3)

Vasomotor symptoms, n (%)

None/Infrequent (< 25% of nights)
Intermittent (25 to < 75% of nights)
Frequent ( 75% of nights)

185 (54.6)
92 (27.1)
62 (18.3)

KPAS domain scores preceding Sleep Study

Active Living Index
Household/Caregiving Index
Sports/Exercise Index

2.32 (0.74)
2.56 (0.80)
2.89 (0.99)

RESULTS
Participant Characteristics
Characteristics of the study sample are summarized in
Table 1. Of the 339 women included in analyses, the mean [SD]
age was 52.2 2.2 years; 48% of the women were Caucasian,
35% were African American, and 17% were Chinese. Approximately 25% of the sample used medications that affect sleep
3 nights per week, and the majority (55%) reported no or infrequent VMS during the Sleep Study protocol.
KPAS domain scores for Active Living, Household/Caregiving, and Sports/Exercise preceding the Sleep Study were
similar in level and mildly correlated with each other (Active
Living and Household/Caregiving: r = 0.13, P = 0.02; Active
Living and Sports/Exercise: r = 0.32, P < 0.001; Household/
Caregiving and Sports/Exercise: r = 0.22, P < 0.001). Compared
to women with a pattern of consistently low or moderate
Sports/Exercise activity, women with a pattern of consistently
high Sports/Exercise activity had significantly increased odds
of having patterns of consistently high Active Living activity
(odds ratio [OR] = 3.32 [95% confidence interval = 2.01, 5.50])
and Household/Caregiving activity (OR = 1.87 [1.11, 3.14]).
Table 2 provides a summary of the sleep characteristics of
the sample. Of note, average PSQI score of the sample was 5.6
3.1 and PSG-assessed TST was 381.0 60.0 min. Approximately 14% of women met diagnostic criteria for insomnia
(n = 47 of 331), 20.2% had at least moderate-severity SDB
(n = 65 of 321), and 8.4% of women had at least moderateseverity PLMS (n = 27 of 323).

KPAS domain patterns over 5-6 years prior to Sleep Study

Active Living activity pattern, n (%)
Consistently Low
71 (20.9)
Inconsistent/Consistently Moderate
166 (49.0)
Consistently High
102 (30.1)
Household/Caregiving activity pattern, n (%)
Consistently Low
Inconsistent/Consistently Moderate
Consistently High

117 (34.5)
133 (39.2)
89 (26.3)

Sports/Exercise activity pattern, n (%)

Consistently Low
Inconsistent/Consistently Moderate
Consistently High

85 (25.1)
161 (47.5)
93 (27.4)

Recent Physical Activity and Sleep

Table 3 summarizes the association between sleep and physical activity levels assessed immediately preceding the SWAN
Sleep Study. No significant associations were observed between
sleep and Active Living or Household/Caregiving Index scores.
In contrast, higher Sports/Exercise Index scores were associated with greater sleep quality and continuity, as assessed by
diary-based measures of restedness ( = 0.16, P < 0.01) and SE
( = 0.14, P = 0.02), respectively, and with greater sleep depth,
as indicated by higher NREM delta power ( = 0.12, P = 0.04)
and lower NREM beta power ( = -0.12, P < 0.05).
Table 4 displays the odds of clinically significant sleep
disturbance according to recent activity levels for each KPAS
domain. The odds of insomnia diagnosis, moderate-severity
SDB, or moderate-severity PLMS did not differ by Active
Living or Household/Caregiving Index value. However,
there were lower odds of meeting diagnostic criteria for

Data are presented as n (%) or mean (standard deviation), as appropriate.

KPAS, Kaiser Physical Activity Survey.

adjusting for previously described covariates. Binary logistic

regression analyses were performed to evaluate the odds of
meeting diagnostic criteria for insomnia (based upon the ISQ),
moderate-severity SDB (AHI 15), and moderate-severity
PLMS (PLMAI 10), as used in previous SWAN Sleep Study
publications.32,35
To evaluate the relationship between sleep and the historical pattern of physical activity (i.e., assessed at up to 4 timepoints in the 5-6 years preceding the Sleep Study), analysis
of covariance (ANCOVA) and logistic regression analyses
SLEEP, Vol. 36, No. 9, 2013

1282

Physical Activity and Sleep in Midlife WomenKline et al

insomnia with higher Sports/Exercise Index scores (OR =

0.68 [0.47, 0.99]).

Table 2SWAN Sleep Study participant sleep characteristics and

prevalence of clinically significant sleep disturbances

Historical Physical Activity Pattern and Sleep

When evaluating the relationship between sleep and different
historical patterns of domain-specific physical activity, no
differences in sleep outcomes were observed across patterns
of Active Living Index activity (data not shown). Polysomnographic TST values significantly differed across Household/
Caregiving Index patterns (F2,313 = 3.13, P = 0.04); women
with consistently high Household/Caregiving values had
greater PSG TST than women with a consistent pattern of low
Household/Caregiving values (P = 0.05). Differences between
Sports/Exercise Index patterns, summarized in Table 5, were
observed for sleep quality (PSQI [F2,317 = 4.17, P = 0.02], diary
restedness [F2,320 = 6.81, P < 0.01]), sleep continuity (diary SE
[F2,320 = 4.39, P = 0.01], PSG SE [F2,316 = 5.25, P < 0.01]), and
sleep depth (NREM power [F2,294 = 3.22, P = 0.04]). For the
majority of these measures, women with a consistently high
level of Sports/Exercise activity had significantly better sleep
compared to women with consistently low Sports/Exercise
activity.
Table 6 displays the odds of clinically significant sleep disturbance according to different patterns of domain-specific activity.
The odds of insomnia diagnosis, moderate-severity SDB,
or moderate-severity PLMS did not differ across patterns of
Active Living or Household/Caregiving Index values. Relative
to consistently low Sports/Exercise Index activity, consistently
high Sports/Exercise Index activity was associated with lower
odds of meeting diagnostic criteria for insomnia (OR = 0.26
[0.08, 0.81]), with a significant linear trend observed (P = 0.02).

5.6 (3.1)
2.0 (0.6)
47 (14.2)

Sleep Duration
Diary total sleep time, min
PSG total sleep time, min

399.1 (51.1)
381.0 (60.0)

Sleep Continuity
Diary sleep efficiency, %
PSG sleep efficiency, %

92.5 (5.3)
84.3 (8.3)

Sleep Depth
NREM power*
NREM power*

76.2 (6.4)
1.8 (1.0)

Sleep Disordered Breathing

AHI
Moderate-severity SDB, n (%)

10.4 (15.3)
65 (20.2)

Periodic Limb Movements During Sleep

PLMAI
Moderate-severity PLMS, n (%)

3.8 (5.3)
27 (8.4)

Data are presented as mean (standard deviation) or n (%), as

appropriate. *Values are expressed as relative units, calculated as the
power within the specific frequency band (in V2/Hz) divided by the total
power across 0.5-32 Hz (in V2/Hz) and multiplied by 100. AHI, apneahypopnea index; NREM, non-rapid eye movement; PLMAI, periodic limb
movement arousal index; PLMS, periodic limb movements during sleep;
PSG, polysomnography; PSQI, Pittsburgh Sleep Quality Index; SDB,
sleep disordered breathing.

DISCUSSION
A growing literature has documented the prevalence
and adverse consequences of sleep disturbance in midlife
women.1,2,6-9 However, we know little about factors which may
protect against sleep disturbance during this period of life.
Physical activity may be one such protective factor, although
the extant literature is equivocal. The present study used a
multi-method approach to investigate the relationship between
physical activity and sleep in midlife women, and several significant associations were noted. Higher levels of Sports/Exercise
activity were consistently associated with important objective
and subjective indices of sleep, whereas Active Living and
Household/Caregiving activity were associated with few sleep
outcomes. Moreover, the relationship between Sports/Exercise
activity and sleep was most robust when considering the pattern
of activity over multiple years relative to activity levels most
proximal to the sleep assessment.
Although household- and lifestyle-related activity make a
prominent contribution to the overall physical activity levels
of midlife women,22 prior studies focused upon the association
between recreational physical activity and sleep.2,14-18 In our
analyses, few relationships emerged between sleep and either
Active Living or Household/Caregiving domains of physical
activity. Because the Active Living and Household/Caregiving
indices of the KPAS predominantly reflect lower-intensity and/
or more intermittent activities,22,36 one possible explanation
is that these domains of physical activity are of insufficient
SLEEP, Vol. 36, No. 9, 2013

Sleep Quality
PSQI, 0-21
Diary restedness, 0-4
Insomnia diagnosis, n (%)

intensity to affect sleep. Although studies directly comparing

the effects of low-, moderate-, and vigorous-intensity physical
activity on sleep have not been conducted, physical activity
interventions for sleep improvement have prescribed moderateand vigorous-intensity physical activity.37-41 Based upon our
results, focusing on recreational physical activity for sleep
improvement seems warranted.
A second key observation was that significantly better sleep,
particularly measures pertaining to sleep quality and continuity,
was observed among women with a consistent pattern of high
Sports/Exercise activity in the 5-6 years leading up to the sleep
assessment. As indicated by the fewer number of significant
relationships observed, these findings were less consistent when
only considering Sports/Exercise activity most recent to the sleep
assessment. It is possible that, given the inherent measurement
error in self-reported physical activity at a single time-point,42,43
repeated assessments of physical activity over time may simply
provide a more accurate view of habitual physical activity.
However, it is also possible that accrual of sleep-related benefits
continue past initial adoption and maintenance of a physically
active lifestyle, as has been documented for most other health
outcomes.44 Unfortunately, the long-term time course of sleep
improvement from exercise is unknown, since randomized trials
longer than 6 months have rarely been conducted,39 and studies
have neglected to assess sleep at intermediate time-points.
Nevertheless, our results suggest that consistent participation in
1283

Physical Activity and Sleep in Midlife WomenKline et al

Table 3Relationship between sleep and recent physical activity (closest preceding Sleep Study) according to physical activity domain
KPAS Domain
Active Living
Sleep Domain
Sleep Quality
PSQIa
Diary restedness, 0-4

Household/Caregiving

Sports/Exercise

B (SE)

B (SE)

B (SE)

-0.06 (0.05)
0.04 (0.05)

-0.07
0.04

-0.01 (0.04)
0.07 (0.04)

-0.01
0.09

-0.06 (0.03)
0.10 (0.04)

-0.09
0.16**

Sleep Duration
Diary total sleep time, min
PSG total sleep time, min

1.42 (4.02)
-6.95 (4.65)

0.02
-0.09

-4.96 (3.63)
1.95 (4.22)

-0.08
0.03

0.01 (3.00)
-4.61 (3.49)

0.00
-0.08

Sleep Continuity
Diary sleep efficiency, %
PSG sleep efficiency, %

0.24 (0.43)
0.03 (0.04)

0.03
0.04

0.20 (0.38)
0.00 (0.03)

0.03
0.00

0.74 (0.32)
-0.04 (0.03)

0.14*
-0.08

Sleep Depth
NREM power,
NREM power,

0.01 (0.01)
0.00 (0.04)

0.04
-0.01

0.01 (0.01)
0.00 (0.03)

0.09
-0.01

0.01 (0.01)
-0.06 (0.03)

0.12*
-0.12*

Sleep Disordered Breathing

AHI

-0.07 (0.07)

-0.05

0.03 (0.07)

0.03

-0.06 (0.05)

-0.06

Periodic Limb Movements During Sleep

PLMAI

-0.01 (0.07)

-0.01

0.02 (0.07)

0.01

0.06 (0.05)

0.07

Data are presented as unstandardized B (standard error [SE]) and standardized coefficients. Analyses adjusted for age, race/ethnicity, marital status,
education, employment status, smoking status, mean daily caffeinated beverages, mean daily alcoholic drinks, use of medication that affects sleep,
menopausal status, vasomotor symptom frequency, and body mass index. aSquare root transformed prior to analyses. Reverse scored (i.e., 100 sleep
efficiency) and natural log (ln) transformed prior to analyses. ln transformed prior to analyses. Values are expressed as relative units, calculated as the
power within the specific frequency band (in V2/Hz) divided by the total power across 0.5-32 Hz (in V2/Hz) and multiplied by 100. ln (plus a constant of 1)
transformed prior to analyses. AHI, apnea-hypopnea index; KPAS, Kaiser Physical Activity Survey; NREM, non-rapid eye movement; PLMAI, periodic limb
movement arousal index; PSG, polysomnography; PSQI, Pittsburgh Sleep Quality Index. For tests of statistical significance: *P < 0.05, **P < 0.01.

Table 4Odds of clinically significant sleep disturbance according to recent domain-specific physical activity (closest preceding Sleep Study)
KPAS Domain
Sleep Disturbance
ISQ: Insomnia diagnosis
PSG: Moderate-severity SDB
PSG: Moderate-severity PLMS

Active Living
OR (95% CI)
0.81 (0.48, 1.34)
1.05 (0.64, 1.71)
1.13 (0.60, 2.12)

Household/Caregiving
OR (95% CI)
0.75 (0.48, 1.16)
0.97 (0.63, 1.51)
0.87 (0.48, 1.56)

Sports/Exercise
OR (95% CI)
0.68 (0.47, 0.99)*
0.97 (0.69, 1.38)
1.14 (0.72, 1.81)

Data presented are odds ratios (95% confidence interval) of meeting each sleep disturbance criterion per 1-unit increase in each respective KPAS domain
score. Analyses adjusted for age, race/ethnicity, marital status, education, employment status, smoking status, mean daily caffeinated beverages, mean
daily alcoholic drinks, use of medication that affects sleep, menopausal status, vasomotor symptom frequency and body mass index. OR, odds ratio; CI,
confidence interval; ISQ, Insomnia Symptom Questionnaire; KPAS, Kaiser Physical Activity Survey; PLMS, periodic limb movements during sleep; PSG,
polysomnography; SDB, sleep disordered breathing. For tests of statistical significance: *P < 0.05.

recreational physical activity may confer additional benefits to

those achieved by more recent activity.
Sports/Exercise Index values were significantly associated
with sleep quality, continuity, and depth, but not duration.
Sports/Exercise activity had perhaps the most consistent relationship with sleep quality, as lower PSQI scores (consistently
high activity only), higher diary-based reports of restedness,
and reduced odds of meeting diagnostic criteria for insomnia
were associated with higher levels of Sports/Exercise activity.
These results concur with prior epidemiologic research,2,14
which concluded that physical activity is associated with less
insomnia-related complaints and/or better subjective sleep in
midlife women. However, they also contrast with findings from
SLEEP, Vol. 36, No. 9, 2013

studies that reported nonsignificant associations between physical activity and sleep quality.15-18
These results are the first to document a relationship between
physical activity and aspects of sleep other than sleep quality
in midlife women, most notably objective indicators of sleep
continuity and depth. Importantly, we observed Sports/Exercise activity to be associated with both subjective (i.e., diary)
and objective (i.e., PSG) assessments of sleep efficiency.
This methodological distinction is noteworthy, as subjective reports of sleep often differ from objective measures
in midlife women.19,20 Moreover, we found that recent and
consistently high levels of Sports/Exercise activity were associated with objective indices of sleep depth, as assessed by
1284

Physical Activity and Sleep in Midlife WomenKline et al

Table 5Sleep according to the historical pattern of KPAS Sports/Exercise activity (i.e., 5-6 years preceding the Sleep Study)
KPAS Sports/Exercise Index Pattern
Sleep Domain
Sleep Quality
PSQI
Diary restedness, 0-4

Consistently Low (1)

Group Comparisons

Inconsistent/Moderate (2) Consistently High (3)

F values

Groupsa

4.17*
6.81**

1,2 > 3
1 < 2,3

6.6 (3.7)
1.8 (0.7)

5.7 (2.9)
2.1 (0.6)

4.5 (2.3)
2.2 (0.5)

Sleep Duration
Diary total sleep time, min
PSG total sleep time, min

394.5 (58.2)
380.3 (58.9)

397.5 (52.3)
375.8 (62.9)

406.3 (40.8)
390.6 (55.1)

Sleep Continuity
Diary sleep efficiency, %
PSG sleep efficiency, %

90.9 (6.4)
82.9 (7.6)

92.5 (5.3)
83.3 (9.6)

94.0 (3.9)
87.2 (5.5)

4.39*
5.25**

1<3
1,2 < 3

Sleep Depth
NREM power,
NREM power,

75.2 (6.9)
2.2 (1.4)

76.0 (6.5)
1.7 (0.8)

77.5 (5.4)
1.7 (0.9)

1.15
3.22*

1>3

Sleep Disordered Breathing

AHI

14.5 (20.4)

10.0 (12.0)

7.3 (14.7)

2.44

2.8 (3.5)

4.4 (5.8)

3.8 (5.6)

2.79

Periodic Limb Movements During Sleep

PLMAI

0.13
0.67

Data presented are unadjusted values [mean (standard deviation)] prior to analyses. Analyses of covariance adjusted for age, race/ethnicity, marital
status, education, employment status, smoking status, mean daily caffeinated beverages, mean daily alcoholic drinks, use of medication that affects sleep,
menopausal status, vasomotor symptom frequency and body mass index. aTukey adjustment for group comparisons. Square root transformed prior to
analyses. Reverse scored (i.e., 100 sleep efficiency) and natural log (ln) transformed prior to analyses. ln transformed prior to analyses. Values expressed
as relative units, calculated as the power within the specific frequency band (in V2/Hz) divided by the total power across 0.5-32 Hz (in V2/Hz) and multiplied
by 100. ln (plus a constant of 1) transformed prior to analyses. AHI, apnea-hypopnea index; KPAS, Kaiser Physical Activity Survey; NREM, non-rapid eye
movement; PLMAI, periodic limb movement arousal index; PSG, polysomnography; PSQI, Pittsburgh Sleep Quality Index. For tests of statistical significance:
*P < 0.05, **P < 0.01.

Table 6Odds of clinically significant sleep disturbance according to historical domain-specific physical activity pattern (i.e., 5-6 years preceding the Sleep
Study)
KPAS Domain
Active Living
OR (95% CI)

Household/Caregiving
OR (95% CI)

ISQ: Insomnia Diagnosis

Consistently Low
Inconsistent/Moderate
Consistently High
Linear trend P

1.00 (referent)
1.18 (0.47, 2.92)
1.76 (0.62, 5.01)
0.28

1.00 (referent)
0.87 (0.39, 1.91)
0.76 (0.29, 1.95)
0.56

1.00 (referent)
0.68 (0.30, 1.52)
0.26 (0.08, 0.81)*
0.02

PSG: Moderate-severity SDB

Consistently Low
Inconsistent/Moderate
Consistently High
Linear trend P

1.00 (referent)
1.52 (0.65, 3.56)
0.63 (0.22, 1.84)
0.44

1.00 (referent)
1.32 (0.62, 2.81)
0.76 (0.30, 1.95)
0.68

1.00 (referent)
0.80 (0.38, 1.71)
0.72 (0.27, 1.92)
0.49

PSG: Moderate-severity PLMS

Consistently Low
Inconsistent/Moderate
Consistently High
Linear trend P

1.00 (referent)
0.75 (0.24, 2.31)
1.00 (0.29, 3.46)
0.96

1.00 (referent)
0.75 (0.30, 1.89)
0.43 (0.12, 1.51)
0.19

1.00 (referent)
1.52 (0.51, 4.50)
1.44 (0.38, 5.40)
0.58

Sleep Disturbance

Sports/Exercise
OR (95% CI)

Data presented are odds ratios (95% confidence interval) of meeting each sleep disturbance criterion for different patterns of each KPAS physical
activity domain, with Consistently Low activity the referent group for each domain. Analyses adjusted for age, race/ethnicity, marital status, education,
employment status, smoking status, mean daily caffeinated beverages, mean daily alcoholic drinks, use of medication that affects sleep, menopausal
status, vasomotor symptom frequency and body mass index. OR, odds ratio; CI, confidence interval; ISQ, Insomnia Symptom Questionnaire; KPAS,
Kaiser Physical Activity Survey; PSG, polysomnography; PLMS, periodic limb movements during sleep; SDB, sleep disordered breathing. For tests of
statistical significance: *P < 0.05.
SLEEP, Vol. 36, No. 9, 2013

1285

Physical Activity and Sleep in Midlife WomenKline et al

spectral analysis of the sleep EEG. Specifically, our findings

of higher NREM delta EEG power (recent Sports/Exercise
activity only) and lower NREM beta EEG power with greater
levels of Sports/Exercise activity conflict with the notion that
exercise primarily impacts subjective, but not objective, sleep
parameters.45 In fact, we are unaware of any other studies that
have linked habitual levels of recreational physical activity
with altered EEG microarchitecture.
No physical activity domains were significantly associated
with PLMS or SDB. The possible relationship between physical
activity and PLMS has been sparsely explored, though experimental research suggests exercise may reduce PLMS severity.13
As our statistical models adjusted for BMI, with which SDB is
strongly associated46 and a pathway by which physical activity
may reduce SDB, it is unsurprising we failed to observe any
significant associations between physical activity and SDB.
Whereas our data are in agreement with others who found a
minimal influence of physical activity on SDB once BMI was
considered,47 other epidemiologic research has reported an
association between exercise and SDB independent of body
composition.48
Strengths of this study include a well-characterized sample
of women from an established cohort study, a comprehensive
multi-modal assessment of sleep, consideration of multiple validated domains of physical activity at several time-points up to
6 years prior to sleep assessment, and statistical adjustment for
several potential confounders. However, these strengths must be
evaluated in light of study limitations. One such limitation is
the lack of multi-modal sleep data from earlier in the SWAN
study. As such, it is possible that persistent poor sleep quality
led to low physical activity during the menopausal transition.
Future research studies would ideally involve randomization
of women with disturbed sleep to an exercise trial prior to the
menopausal transition with longitudinal follow-up through postmenopause. Another limitation is that additional factors that
were not considered in these analyses (e.g., mental health, environmental influences) could account for the findings. However,
it is noteworthy that significant relationships between physical
activity and sleep were observed despite statistical adjustment
for key factors which could mediate this relationship (e.g.,
BMI, other health behaviors). An additional limitation is that
our findings may not generalize to all women. For example, in
a smaller SWAN ancillary study of predominantly postmenopausal women with frequent VMS, greater household-related
activity was associated with better subjective sleep.49 Although
race and menopausal status, among others, could potentially
be important moderators of the relationship between physical
activity and sleep, we did not have an adequate sample size to
investigate these potential interactions. In the future, it will be
important to evaluate whether these factors moderate the relationship between physical activity and sleep. A further limitation
is the reliance upon self-report physical activity data. Subjective and objective assessments of physical activity are only
modestly correlated,22 with objective assessment indicating
much less physical activity than self-reported.50 Specifically, the
KPAS does not permit detailed inquiry of the specific activities
reported (e.g., timing, intensity, volume) and absolute amounts
of physical activity performed. Consequently, its best use may
be for ranking levels of activity, as were performed in this study.
SLEEP, Vol. 36, No. 9, 2013

Similarly, inconsistent patterns of physical activity over 5-6

years were grouped with consistently moderate patterns
of physical activity in analyses. Although we did not have an
adequate sample size to examine more specific subgroups, future
research should endeavor to classify inconsistent activity
patterns in a more precise manner when possible.
Despite these limitations, the study results supplement
the existing literature on the benefits of physical activity on
numerous other symptoms and health conditions that arise
during the menopausal transition (e.g., depression, weight
gain, reduced bone density).51 In particular, the potential use of
physical activity as a nonpharmacologic treatment or preventive measure for sleep disturbance among midlife women is
appealing, given that physical activity is a modifiable behavior
with minimal side effects and the robust associations between
consistent recreational physical activity and indices of sleep
quality, continuity and depth that were noted herein. Randomized trials are needed to address the limitations of previous
interventions that have evaluated the efficacy of exercise on
sleep quality in midlife women, such as inclusion of women
without sleep complaints,37,39-41 reliance upon subjective sleep
measures,37-41 and failure to account for VMS.39,41
In summary, these results suggest that higher levels of recreational physical activity, but not lifestyle- or household-related
activity, are associated with better sleep in midlife women, and
that consistently high levels of activity are more robustly associated with better sleep than recent activity. Although experimental trials are needed to confirm these observations, adoption
and/or maintenance of adequate recreational physical activity
may help to improve sleep and protect against sleep disturbances that arise during midlife in women.
ACKNOWLEDGMENTS
The authors thank the study staff at each site and all the women
who participated in SWAN. The Study of Womens Health Across
the Nation (SWAN) has grant support from the National Institutes of Health (NIH), DHHS, through the National Institute on
Aging (NIA), the National Institute of Nursing Research (NINR)
and the NIH Office of Research on Womens Health (ORWH)
(Grants U01NR004061, U01AG012505, U01AG012535,
U01AG012531, U01AG012539, U01AG012546, U01AG012553,
U01AG012554, U01AG012495). The SWAN Sleep Study was
funded by the NIH (Grants R01AG019360, R01AG019361,
R01AG019362, R01AG019363). Sleep data were processed with
the support of UL1RR024153. Additional NIH grant support
for Dr. Kline and Dr. Irish was provided by T32HL082610 and
T32MH019986 respectively, and grant support for Dr. Krafty was
provided by National Science Foundation DMS-0805050. The
content of this paper is solely the responsibility of the authors and
does not necessarily represent the official views of the NSF, NIA,
NINR, ORWH or the NIH.
Clinical Centers
University of Michigan, Ann Arbor Siobn Harlow, PI
2011-present, MaryFran Sowers, PI 1994-2011; Massachusetts
General Hospital, Boston, MA Joel Finkelstein, PI 1999present; Robert Neer, PI 1994-1999; Rush University, Rush
University Medical Center, Chicago, IL Howard Kravitz,
PI 2009-present; Lynda Powell, PI 1994-2009; University of
1286

Physical Activity and Sleep in Midlife WomenKline et al

California, Davis/Kaiser Ellen Gold, PI; University of California, Los Angeles Gail Greendale, PI; Albert Einstein
College of Medicine, Bronx, NY Carol Derby, PI 2011present, Rachel Wildman, PI 2010-2011; Nanette Santoro, PI
2004-2010; University of Medicine and Dentistry New Jersey
Medical School, Newark Gerson Weiss, PI 1994-2004; and the
University of Pittsburgh, Pittsburgh, PA Karen Matthews, PI.

10. Youngstedt SD, Kline CE. Epidemiology of exercise and sleep. Sleep
Biol Rhythms 2006;4:215-21.
11. Reid KJ, Baron KG, Lu B, Naylor E, Wolfe L, Zee PC. Aerobic exercise
improves self-reported sleep and quality of life in older adults with
insomnia. Sleep Med 2010;11:934-40.
12. Kline CE, Crowley EP, Ewing GB, et al. The effect of exercise training on
obstructive sleep apnea and sleep quality: a randomized controlled trial.
Sleep 2011;34:1631-40.
13. Esteves AM, de Mello MT, Pradella-Hallinan M, Tufik S. Effect of acute
and chronic physical exercise on patients with periodic leg movements.
Med Sci Sports Exerc 2009;41:237-42.
14. Li C, Borgfeldt C, Samsioe G, Lidfeldt J, Nerbrand C. Background factors
influencing somatic and psychological symptoms in middle-age women
with different hormonal status: a population-based study of Swedish
women. Maturitas 2005;52:306-18.
15. Woods NF, Mitchell ES. Sleep symptoms during the menopausal
transition and early postmenopause: observations from the Seattle Midlife
Womens Health Study. Sleep 2010;33:539-49.
16. Pien GW, Sammel MD, Freeman EW, Lin H, DeBlasis TL. Predictors of
sleep quality in women in the menopausal transition. Sleep 2008;31:991-9.
17. Di Donato P., Giulini NA, Bacchi MA, Cicchetti G, Progetto Menopausa
Italia Study Group. Factors associated with climacteric symptoms in
women around menopause attending menopause clinics in Italy. Maturitas
2005;52:181-9.
18. Tom SE, Kuh D, Guralnik JM, Mishra GD. Self-reported sleep difficulty
during the menopausal transition: results from a prospective cohort study.
Menopause 2010;17:1128-35.
19. Young T, Rabago D, Zgierska A, Austin D, Laurel F. Objective and
subjective sleep quality in premenopausal, perimenopausal, and
postmenopausal women in the Wisconsin Sleep Cohort Study. Sleep
2003;26:667-72.
20. Freedman RR, Roehrs TA. Lack of sleep disturbance from menopausal
hot flashes. Fertil Steril 2004;82:138-44.
21. Kubitz KA, Landers DM, Petruzzello SJ, Han M. The effects of acute
and chronic exercise on sleep: a meta-analytic review. Sports Med
1996;21:277-91.
22. Ainsworth BE, Sternfeld B, Richardson MT, Jackson K. Evaluation of
the Kaiser Physical Activity Survey in women. Med Sci Sports Exerc
2000;32:1327-38.
23. Masse LC, Ainsworth BE, Tortolero S, et al. Measuring physical activity
in midlife, older, and minority women: issues from an expert panel. J
Womens Health 1998;7:57-67.
24. Hallal PC, Victora CG, Wells JC, Lima RC. Physical inactivity:
prevalence and associated variables in Brazilian adults. Med Sci Sports
Exerc 2003;35:1894-1900.
25. Sowers MF, Crawford S, Sternfeld B, et al. SWAN: a multi-center, multiethnic, community-based cohort study of women and the menopausal
transition. In: Lobo RA, Kelsey J, Marcus R, eds. Menopause: biology
and pathobiology. San Diego: Academic Press; 2000:175-88.
26. Baecke JA, Burema J, Frijters JE. A short questionnaire for the
measurement of habitual physical activity in epidemiological studies. Am
J Clin Nutr 1982;36:936-42.
27. Rechtschaffen A, Kales A. A manual of standardized terminology,
techniques and scoring system for sleep stages of human subjects (NIH
Publication 204). Washington, DC: U.S. Government Printing Office,
Department of Health Education and Welfare; 1968.
28. American Academy of Sleep Medicine Task Force. Sleep-related
breathing disorders in adults: recommendations for syndrome definition
and measurement techniques in clinical research. Sleep 1999;22:667-89.
29. American Sleep Disorders Association Atlas Task Force. Recording and
scoring leg movements. Sleep 1993;16:748-59.
30. Brunner DP, Vasko RC, Detka CS, Monahan JP, Reynolds CF III, Kupfer
DJ. Muscle artifacts in the sleep EEG: automated detection and effect on
all-night EEG power spectra. J Sleep Res 1996;5:155-64.
31. Buysse DJ, Reynolds CF III, Monk TH, Berman SR, Kupfer DJ. The
Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice
and research. Psychiatry Res 1989;28:193-213.
32. Okun ML, Kravitz HM, Sowers MF, Moul DE, Buysse DJ, Hall M.
Psychometric evaluation of the Insomnia Symptom Questionnaire: a
self-report measure to identify chronic insomnia. J Clin Sleep Med
2009;5:41-51.
33. World Health Organization. Guidelines for ATC classification. Available
at: http://www.whocc.no/atcddd. Accessed December 10, 2007.

NIH Program Office

National Institute on Aging, Bethesda, MD Winifred Rossi
2012-present; Sherry Sherman 1994-2012; Marcia Ory 19942001; National Institute of Nursing Research, Bethesda, MD
Program Officers.
Central Laboratory
University of Michigan, Ann Arbor Daniel McConnell
(Central Ligand Assay Satellite Services).
Coordinating Center
University of Pittsburgh, Pittsburgh, PA Maria Mori
Brooks, PI 2012-present; Kim Sutton-Tyrrell, PI 2001-2012;
New England Research Institutes, Watertown, MA - Sonja
McKinlay, PI 1995-2001.
Steering Committee
Susan Johnson, Current Chair; Chris Gallagher, Former Chair.
DISCLOSURE STATEMENT
This was not an industry supported study. Dr. Buysse has
served as a paid consultant on scientific advisory boards for Eisai,
GlaxoSmithKline, Merck, Philips Respironics, Purdue Pharma,
Sanofi-Aventis, and Takeda. He has also spoken at single-sponsored educational meetings for Sanofi-Aventis and Servier. The
other authors have indicated no financial conflicts of interest.
REFERENCES

1. Kravitz HM, Ganz PA, Bromberger J, Powell LH, Sutton-Tyrrell K,

Meyer PM. Sleep difficulty in women at midlife: a community survey of
sleep and the menopausal transition. Menopause 2003;10:19-28.
2. Arakane M, Castillo C, Rosero MF, Penafiel R, Perez-Lopez FR,
Chedraui P. Factors relating to insomnia during the menopausal transition
as evaluated by the Insomnia Severity Index. Maturitas 2011;69:157-61.
3. Chedraui P, Perez-Lopez FR, Mendoza M, et al. Factors related to
increased daytime sleepiness during the menopausal transition as
evaluated by the Epworth Sleepiness Scale. Maturitas 2010;65:75-80.
4. Cappuccio FP, DElia L, Strazzullo P, Miller MA. Quantity and quality
of sleep and incidence of type 2 diabetes: a systematic review and metaanalysis. Diabetes Care 2010;33:414-20.
5. Elwood P, Hack M, Pickering J, Hughes J, Gallacher J. Sleep disturbance,
stroke, and heart disease events: evidence from the Caerphilly cohort. J
Epidemiol Community Health 2006;60:69-73.
6. Al-Delaimy WK, Manson JE, Willett WC, Stampfer MJ, Hu FB. Snoring
as a risk factor for type II diabetes mellitus: a prospective study. Am J
Epidemiol 2002;155:387-93.
7. Leineweber C, Kecklund G, Akerstedt T, Janszky I, Orth-Gomer K.
Snoring and the metabolic syndrome in women. Sleep Med 2003;4:531-6.
8. Hall MH, Okun ML, Sowers MF, et al. Sleep is associated with the
metabolic syndrome in a multi-ethnic cohort of midlife women: the
SWAN Sleep Study. Sleep 2012;35:783-90.
9. Campos-Rodriguez F, Martinez-Garcia MA, de la Cruz-Moron I,
Almeida-Gonzalez C, Catalan-Serra P, Montserrat JM. Cardiovascular
mortality in women with obstructive sleep apnea with or without
continuous positive airway pressure treatment: a cohort study. Ann Intern
Med 2012;156:115-22.

SLEEP, Vol. 36, No. 9, 2013

1287

Physical Activity and Sleep in Midlife WomenKline et al

43. Shephard RJ. Limits to the measurement of habitual physical activity by

questionnaires. Br J Sports Med 2003;37:197-206.
44. Pedersen BK, Saltin B. Evidence for prescribing exercise as therapy in
chronic disease. Scand J Med Sci Sports 2006;16 Suppl 1:3-63.
45. Buman MP, King AC. Exercise as a treatment to enhance sleep. Am J
Lifestyle Med 2010;4:500-14.
46. Li C, Ford ES, Zhao G, Croft JB, Balluz LS, Mokdad AH. Prevalence of
self-reported clinically diagnosed sleep apnea according to obesity status
in men and women: National Health and Nutrition Examination Survey,
2005-2006. Prev Med 2010;51:18-23.
47. Awad KM, Malhotra A, Barnet JH, Quan SF, Peppard PE. Exercise is
associated with a reduced incidence of sleep-disordered breathing. Am J
Med 2012;125:485-90.
48. Peppard PE, Young T. Exercise and sleep-disordered breathing: an
association independent of body habitus. Sleep 2004;27:480-4.
49. Lambiase MJ, Thurston RC. Physical activity and sleep among midlife
women with vasomotor symptoms. Menopause 2013 Mar 25. [Epub
ahead of print]
50. Troiano RP, Berrigan D, Dodd KW, Masse LC, Tilert T, McDowell M.
Physical activity in the United States measured by accelerometer. Med Sci
Sports Exerc 2008;40:181-8.
51. Daley AJ, Stokes-Lampard HJ, Macarthur C. Exercise to reduce vasomotor
and other menopausal symptoms: a review. Maturitas 2009;63:176-80.

34. Kravitz HM, Avery E, Sowers M et al. Relationships between menopausal

and mood symptoms and EEG sleep measures in a multi-ethnic sample
of middle-aged women: the SWAN Sleep Study. Sleep 2011;34:1221-32.
35. Hall MH, Matthews KA, Kravitz HM, et al. Race and financial strain
are independent correlates of sleep in midlife women: the SWAN Sleep
Study. Sleep 2009;32:73-82.
36. Ainsworth BE, Haskell WL, Herrmann SD, et al. 2011 Compendium of
Physical Activities: a second update of codes and MET values. Med Sci
Sports Exerc 2011;43:1575-81.
37. Elavsky S, McAuley E. Lack of perceived sleep improvement after
4-month structured exercise programs. Menopause 2007;14:535-40.
38. Mansikkamaki K, Raitanen J, Nygard CH, et al. Sleep quality and aerobic
training among menopausal women: a randomized controlled trial.
Maturitas 2012;72:339-45.
39. Tworoger SS, Yasui Y, Vitiello MV, et al. Effects of a yearlong moderateintensity exercise and a stretching intervention on sleep quality in
postmenopausal women. Sleep 2003;26:830-6.
40. Wilbur J, Miller AM, McDevitt J, Wang E, Miller J. Menopausal status,
moderate-intensity walking, and symptoms in midlife women. Res
Theory Nurs Pract 2005;19:163-80.
41. Kline CE, Sui X, Hall MH, et al. Dose-response effects of exercise training
on the subjective sleep quality of postmenopausal women: exploratory
analyses of a randomised controlled trial. BMJ Open 2012;2:e001044.
42. Ferrari P, Friedenreich C, Matthews CE. The role of measurement error in
estimating levels of physical activity. Am J Epidemiol 2007;166:832-40.

SLEEP, Vol. 36, No. 9, 2013

1288

Physical Activity and Sleep in Midlife WomenKline et al