CALYPSO: Adapting Sleep and Yoga Interventions for Maximal Effectiveness in Low Income Populations

Sponsor
Brigham and Women's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03392194
Collaborator
National Center for Complementary and Integrative Health (NCCIH) (NIH)
33
1
2
6
5.5

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the feasibility of conducting a future randomized control trial that will compare the efficacy of sleep behavioral interventions in a high-risk community including adapted sleep hygiene and yoga. The investigators will conduct a 40 person 12-week randomized control trial (RCT) in low-income housing population where half the participants will receive a community adapted sleep hygiene intervention (SH) and half will receive a community adapted sleep hygiene intervention and a yoga intervention. The investigators will evaluate the feasibility of recruiting from our target community, randomizing individuals to interventions delivered in community rooms with home-based practices, and delivering the targeted interventions with high adherence and fidelity.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Sleep hygiene intervention
  • Behavioral: Yoga intervention
N/A

Detailed Description

Inadequate sleep is highly prevalent in low-socioeconomic status (SES) and minority groups and associated with multiple health problems. The root causes of inadequate sleep are often related to behavioral practices and stress, both of which may be favorably impacted using socio-contextually appropriate sleep hygiene recommendations and mind-body practices such as yoga. A preliminary RCT that will address the role of sleep behavioral interventions in a high-risk community will be conducted. This evidence is needed to guide mind-body therapies in low-SES communities in which such strategies are under-utilized to improve health.

The investigators have assembled a multidisciplinary team of experts in sleep medicine, complementary and integrative health, behavioral medicine, community engagement, social epidemiology, and clinical trials to conduct a planning study to adapt behavioral sleep interventions for residents in urban low-income housing and to evaluate their uptake and fidelity. The investigators have conducted qualitative formative evaluation work and conducted modified SH and Yoga pilot studies. In this phase, the investigators will deliver a 12-week trial testing the feasibility of (1) an adapted sleep hygiene intervention (SH) and (2) yoga + adapted sleep hygiene intervention SH+Y):

  1. A Sleep Hygiene (SH) Intervention, addressing: beliefs and attitudes towards sleep; challenges for adhering to sleep hygiene recommendations given chaotic family routines, work schedules and bedroom conditions; strategies for overcoming barriers, and prioritization of recommendations most likely to be efficacious.

  2. A Yoga (Y) Intervention: intervention intensity/duration and class format; tailored home-based recommendations for bedtime practice combining meditation, breathing and postures; tools to assess and enhance adherence; race/ethnicity concordance of the instructor and student; and use of peer yoga assistants.

The investigators aim to conduct a 40 person 12-week RCT of SH vs SH+Y to inform the design of a future large-scale RCT. The investigators will evaluate the feasibility of recruiting from our target community, randomizing individuals to interventions delivered in community rooms with home-based practices, and delivering the targeted interventions with high adherence and fidelity. The following will be evaluated:

  • Reach of the target population: The number of potentially eligible individuals approached to participate will be tracked as well as the characteristics of individuals who do and do not choose to participate, and differences will be assessed. Reasons for choosing not to participate will be assessed using open ended questions (e.g., burden, perception of yoga, needs, etc.).

  • Adoption and adherence: the proportion of individuals that sustain participation throughout the intervention will be assessed, and quantify attendance at classes and home-practices through logs and interim phone interviews. The investigators will describe patterns of dropout rates and adherence to the interventions by key demographic factors and by moderating and mediating factors.

  • Implementation-consistency of delivery of the intervention: a checklist of core intervention elements will be used to document the degree to which core elements of the intervention was delivered as specified in the protocol.

The investigators will also assess the feasibility of collecting a range of baseline, outcome, process and mediator data and to generate data to support use of specific measures in a later trial, including patterns of missingness of data, distributions of data, correlations between outcomes, baseline factors and mediators, and evaluation of "dose-response" associations between time in intervention and sleep duration and efficiency.

Power analysis (sample size, evaluable subjects, etc.): The study is designed for feasibility and not powered to test the intervention effect. The SH+Y intervention will be considered as potentially efficacious if the estimates for the change scores (post-pre within and between group changes and their 95% confidence intervals) are consistent with clinically significant improvements in sleep duration (actigraphy sleep increases by > 30 minutes), sleep quality improves by > 0.3 standard deviations), or sleep hygiene (reduction in deviation in wake time relative to recommended wake time > 25%). The investigators will consider inclusion of specific measurements (mediators) in a future RCT based on: <10% missingness; correlation of change score or baseline score with outcomes of >.20; absence of redundancy with a simpler metric (r<.80).

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Adapting Sleep and Yoga Interventions for Maximal Effectiveness in Low Income Populations
Actual Study Start Date :
Jan 10, 2018
Actual Primary Completion Date :
Jun 29, 2018
Actual Study Completion Date :
Jul 12, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sleep hygiene & Yoga (SH+Y)

Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. After completing the SH sessions, they will receive 10 weeks of the yoga intervention (8 in-person yoga sessions and 2 weeks of yoga home practice maintenance assessment).

Behavioral: Sleep hygiene intervention
The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal.

Behavioral: Yoga intervention
Following the SH intervention, participants randomized to the SH+Y arm will participate in 8 weekly beginner level yoga classes. Classes will increase participants' skill and comfort with yoga postures and relaxing breathing exercises so that participants can adopt an evening yoga practice (10 weeks).

Active Comparator: Sleep hygiene (SH)

Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment.

Behavioral: Sleep hygiene intervention
The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal.

Outcome Measures

Primary Outcome Measures

  1. Sleep Duration [12 weeks]

    Change in sleep duration from baseline to follow-up measure by actigraphs. We will conduct a repeated measures ANCOVA, modeling time, intervention group and a time*intervention interaction. We will explore change in stress, anxiety, depressive symptoms, mindfulness, and sleep hygiene score as potential explanatory variables.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Verbally proficient in English

  • Self-reported average (over the prior month) weekday sleep duration of < 6 hours

  • Reside in a public housing

Exclusion Criteria:
  • Severe physical conditions preventing participation in yoga, including major surgery or head injury in the prior 3 months, or unstable vertebral injury with inability to sit or lie down for 5 or more minutes; or glaucoma

  • Major psychiatric disease (e.g. schizophrenia, depression, PTSD) resulting in hospitalization in the last year; or disease severity that, in the opinion of the investigator, would make it difficult for the participant to partake in the study activities.

  • Severe sleep disorders: self-report of physician diagnosed insomnia requiring hypnotics more than 3 times/ week or an untreated known sleep disorder (sleep apnea, RLS), that in the opinion of the investigator, would make it difficult for the participant to achieve sleep hygiene goals.

  • Needing an assistive device such as a walker or cane, frequent falls, history of stroke resulting in weakness or numbness interfering with moving easily, or other problems causing ongoing balance issues and difficulty walking

  • Yoga class participation in last 6 weeks

  • Known pregnancy.

  • Participation in prior sleep and yoga study pilots

Contacts and Locations

Locations

Site City State Country Postal Code
1 Brigham and Women's Hospital Boston Massachusetts United States 02115

Sponsors and Collaborators

  • Brigham and Women's Hospital
  • National Center for Complementary and Integrative Health (NCCIH)

Investigators

  • Principal Investigator: Susan Redline, MD, MPH, Brigham and Women's Hospital

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
Susan Redline, Professor, Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT03392194
Other Study ID Numbers:
  • 2017P002349
  • 1R34AT008923-01
First Posted:
Jan 5, 2018
Last Update Posted:
Sep 11, 2019
Last Verified:
Sep 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Susan Redline, Professor, Brigham and Women's Hospital

Study Results

Participant Flow

Recruitment Details From January-March 2018, participants were recruited from two affordable housing communities. Convenience and snowball sampling methods were employed. Study staff and community partners provided information to interested participants at community events and distributed flyers and postcards throughout the communities.
Pre-assignment Detail Sleep hygiene (SH) group sessions served as a run-in period for randomization. Participants were consented to participate in the research study (n=38) and then attended two SH group session. At the end of the second SH session, participants were randomized to the SH-arm or the sleep hygiene and yoga (SH+Y) arm (n=33).
Arm/Group Title Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH)
Arm/Group Description Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. After completing the SH sessions, they will receive 10 weeks of the yoga intervention (8 in-person yoga sessions and 2 weeks of yoga home practice maintenance assessment). Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal. Yoga intervention: Following the SH intervention, participants randomized to the SH+Y arm will participate in 8 weekly beginner level yoga classes. Classes will increase participants' skill and comfort with yoga postures and relaxing breathing exercises so that participants can adopt an evening yoga practice (10 weeks). Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal.
Period Title: Overall Study
STARTED 16 17
COMPLETED 14 15
NOT COMPLETED 2 2

Baseline Characteristics

Arm/Group Title Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH) Total
Arm/Group Description Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. After completing the SH sessions, they will receive 10 weeks of the yoga intervention (8 in-person yoga sessions and 2 weeks of yoga home practice maintenance assessment). Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal. Yoga intervention: Following the SH intervention, participants randomized to the SH+Y arm will participate in 8 weekly beginner level yoga classes. Classes will increase participants' skill and comfort with yoga postures and relaxing breathing exercises so that participants can adopt an evening yoga practice (10 weeks). Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal. Total of all reporting groups
Overall Participants 16 17 33
Age (Count of Participants)
<=18 years
0
0%
0
0%
0
0%
Between 18 and 65 years
14
87.5%
15
88.2%
29
87.9%
>=65 years
2
12.5%
2
11.8%
4
12.1%
Age (years) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [years]
44.44
(14.74)
47.29
(10.83)
45.91
(13.09)
Sex: Female, Male (Count of Participants)
Female
15
93.8%
15
88.2%
30
90.9%
Male
1
6.3%
2
11.8%
3
9.1%
Ethnicity (NIH/OMB) (Count of Participants)
Hispanic or Latino
6
37.5%
7
41.2%
13
39.4%
Not Hispanic or Latino
10
62.5%
9
52.9%
19
57.6%
Unknown or Not Reported
0
0%
1
5.9%
1
3%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native
0
0%
1
5.9%
1
3%
Asian
2
12.5%
1
5.9%
3
9.1%
Native Hawaiian or Other Pacific Islander
0
0%
0
0%
0
0%
Black or African American
6
37.5%
8
47.1%
14
42.4%
White
3
18.8%
2
11.8%
5
15.2%
More than one race
2
12.5%
3
17.6%
5
15.2%
Unknown or Not Reported
3
18.8%
2
11.8%
5
15.2%
Sleep Duration (minutes/night) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [minutes/night]
400.69
(75.45)
418.06
(66.07)
409.37
(70.24)

Outcome Measures

1. Primary Outcome
Title Sleep Duration
Description Change in sleep duration from baseline to follow-up measure by actigraphs. We will conduct a repeated measures ANCOVA, modeling time, intervention group and a time*intervention interaction. We will explore change in stress, anxiety, depressive symptoms, mindfulness, and sleep hygiene score as potential explanatory variables.
Time Frame 12 weeks

Outcome Measure Data

Analysis Population Description
The missing count is based on 21 participants having adequate quality actigraphy data at both baseline and endpoint
Arm/Group Title Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH)
Arm/Group Description Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. After completing the SH sessions, they will receive 10 weeks of the yoga intervention (8 in-person yoga sessions and 2 weeks of yoga home practice maintenance assessment). Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal. Yoga intervention: Following the SH intervention, participants randomized to the SH+Y arm will participate in 8 weekly beginner level yoga classes. Classes will increase participants' skill and comfort with yoga postures and relaxing breathing exercises so that participants can adopt an evening yoga practice (10 weeks). Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal.
Measure Participants 11 14
Mean (Standard Deviation) [minutes/night]
-0.91
(43.87)
-2.93
(66.92)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Sleep Hygiene & Yoga (SH+Y), Sleep Hygiene (SH)
Comments Null hypothesis: There is no difference in change in sleep duration between the two intervention arms.
Type of Statistical Test Other
Comments The purpose of this small pilot randomized control trial (RCT) was to assess feasibility and acceptability of conducting community based sleep hygiene and yoga interventions, to be scaled and tested in a future, larger RCT.
Statistical Test of Hypothesis p-Value 0.932
Comments
Method t-test, 2 sided
Comments Due to main findings, analysis to explore potential mediators of effect were not pursued, despite original plan to explore explanatory variables.
Method of Estimation Estimation Parameter Mean Difference (Net)
Estimated Value -2.02
Confidence Interval (2-Sided) 95%
-46.35 to 50.39
Parameter Dispersion Type:
Value:
Estimation Comments

Adverse Events

Time Frame Five months.
Adverse Event Reporting Description
Arm/Group Title Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH)
Arm/Group Description Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. After completing the SH sessions, they will receive 10 weeks of the yoga intervention (8 in-person yoga sessions and 2 weeks of yoga home practice maintenance assessment). Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal. Yoga intervention: Following the SH intervention, participants randomized to the SH+Y arm will participate in 8 weekly beginner level yoga classes. Classes will increase participants' skill and comfort with yoga postures and relaxing breathing exercises so that participants can adopt an evening yoga practice (10 weeks). Participants will receive the sleep hygiene intervention, which includes 2 sleep hygiene sessions and 10 weeks of maintenance assessment. Sleep hygiene intervention: The community-adapted SH intervention includes 2 group sessions. (1) teach the importance of sleep and the core components of SH; distribute and explain the daily sleep log (2) facilitate an open discussion where participants share challenges and experiences implementing a SH goal.
All Cause Mortality
Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH)
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/16 (0%) 0/17 (0%)
Serious Adverse Events
Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH)
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/16 (0%) 0/17 (0%)
Other (Not Including Serious) Adverse Events
Sleep Hygiene & Yoga (SH+Y) Sleep Hygiene (SH)
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 8/16 (50%) 6/17 (35.3%)
Cardiac disorders
Arm and chest pain 2/16 (12.5%) 2 0/17 (0%) 0
Ear and labyrinth disorders
Ear infection 0/16 (0%) 0 1/17 (5.9%) 1
Eye disorders
Scratched cornea 0/16 (0%) 0 1/17 (5.9%) 1
Infections and infestations
Cellulitis (foot) 0/16 (0%) 0 1/17 (5.9%) 2
Root canal infection 1/16 (6.3%) 1 0/17 (0%) 0
Infection 0/16 (0%) 0 1/17 (5.9%) 2
Musculoskeletal and connective tissue disorders
Back pain/spasm 3/16 (18.8%) 3 2/17 (11.8%) 2
Leg pain 2/16 (12.5%) 2 1/17 (5.9%) 1
Skin and subcutaneous tissue disorders
Mild rash (actigraph) 0/16 (0%) 0 2/17 (11.8%) 3

Limitations/Caveats

This study was a developmental pilot to test novel interventions in the community. At this stage, sample sizes were not developed to achieve power and statistically reliable results.

More Information

Certain Agreements

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Dr. Susan Redline
Organization Brigham and Women's Hospital
Phone 617-732-5859
Email SREDLINE@BWH.HARVARD.EDU
Responsible Party:
Susan Redline, Professor, Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT03392194
Other Study ID Numbers:
  • 2017P002349
  • 1R34AT008923-01
First Posted:
Jan 5, 2018
Last Update Posted:
Sep 11, 2019
Last Verified:
Sep 1, 2019