Skip to content

Improving Sleep in Veterans and Their CGs

Improving Sleep In Veterans and Their Family Caregivers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02057068
Acronym
SLEEP-E Dyads
Enrollment
102
Registered
2014-02-06
Start date
2014-11-30
Completion date
2016-07-31
Last updated
2018-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Quality

Keywords

Caregivers, Telemedicine, Sleep Disorders, Meditation, Cognitive Behavioral Therapy, Activity Enhancement, Technology, Non-pharmacological sleep intervention

Brief summary

This study addresses the neglected topic of sleep disturbance in older caregiving dyads-a topic that has important implications for the safety, health, functioning and quality of life of older Veterans living at home and being cared for by a family caregiver (CG). The purpose of the study was to develop and field test non-pharmacological, technology enhanced sleep hygiene, exercise and meditation interventions to improve sleep in Veteran caregiving dyads.The conceptual framework of the intervention incorporated components of cognitive behavioral therapy, psycho-education and self-management support for individuals with chronic conditions with an emphasis on cultivating competence and mastery.

Detailed description

Research Plan: Sample. Veteran care receivers(CR s) or carepartners (CP) over the age of 60 who require assistance from a spousal or cohabitating caregiver (CG) and Veteran caregivers providing care for a cohabitating carepartner were recruited. Dyads underwent comprehensive baseline assessments consisting of in-person home-based interviews and iPad training (T1) followed by a week-long data collection of contemporaneous actigraphic sleep parameters and twice daily (morning and evening) indices of subjective sleep, activity, mood, behavior and sleep hygiene completed on the Tonic for Health Platform. Dyads were randomly assigned to an immediate intervention or wait-list control group. The immediate group received the intervention described below followed by post-intervention assessments (T2) identical to baseline. Wait-list participants then received the intervention followed by a final post-intervention assessment for the wait-list group only (T3). Intervention. Daily Videos: Video modules were delivered daily to the dyads' iPads during the 6-week intervention. All participants received core programming of sleep hygiene education, and guided instruction for daily physical activity enhancement Move-Out! and meditation/relaxation/self-care Stand Down! sessions individualized to functional ability levels. The baseline data allowed for subsequent compilation and programming of individualized, algorithmically derived, adaptive prescriptions for relevant video modules, sleep hygiene recommendations and cognitive behavioral strategies based upon the three independent streams of objective and subjective data for each dyad member. During the intervention dyads completed brief morning and evening diaries to assess compliance with the intervention and capture daily mood and sleep/sleep hygiene data. Tele-Video-Conferences: Each dyad participated in two tele-video conferences with the PI. The first was to discuss evaluation results, obtain buy-in for the prescribed intervention and address dysfunctional beliefs and attitudes about sleep. The second call was a check-in, encouragement, reinforcement and coaching call. Dyads were re-assessed following the 6-week intervention. Evaluations: Standardized quantitative evaluations regarding the utility of the program were completed following the post-intervention assessments on the iPads. A sub-sample of dyads also participated in qualitative interviews.

Interventions

BEHAVIORALSLEEP-E Dyads Intervention

Described in arm/group description

Sponsors

Emory University
CollaboratorOTHER
VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

This efficacy study was not blinded.

Intervention model description

Randomization to an immediate intervention group or a no-contact wait list control group. Following post intervention assessments the wait-list control group received the intervention.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Care recipient must be age 60 and over and require assistance from the identified caregiver with more than one Activity of Daily Living or three or more Instrumental Activities of Daily Living, * have a life expectancy of greater than or equal to six (6) months, * have no plans for transitioning out of home in the next six months, * and have approval from the primary care provider to participate in the research. * Caregivers must live with care recipient * Caregivers must obtain a negative mini-cog assessment or negative TICS-m assessment. Caregivers can be any relation (spouse, child, sibling, friend, etc.) to the care recipient so long as the two are cohabitating. * Caregiver can be any age. * For Phase 2 and Phase 3 of the study, either the care recipient or the caregiver must have difficulty sleeping as indicated by scores on the Insomnia Severity Index.

Exclusion criteria

* Parkinson's with tremor or other movement disorder that would invalidate actigraphy * Untreated diagnosis of sleep apnea or restless leg syndrome * Inability to tolerate actigraphy * CG and CR sleep efficiency \> 85% and/or both members of dyad report sleeping well * Caregivers must have a negative screen with the Mini-Cog or the ModifiedTelephone Interview for Cognitive Status (TICS-M) to demonstrate cognitive capacity to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Subjective Sleep QualityBaseline (T1) and Post-Intervention (T2) - 8 WeeksPittsburgh Sleep Quality Index Scores (PSQI) The Pittsburgh Sleep Quality Index is a standardized and validated measure of subjective sleep quality and sleep disturbance. The inventory has 18-items. PSQI scores range from 0 - 21. A total score \> 5 (some evidence for 8) is indicative of poor sleep quality.

Secondary

MeasureTime frameDescription
Mean Sleep EfficiencyBaseline (T1) and Post-Intervention (T2) - 8 WeeksAverage sleep efficiency over 7 nights of actigraphic measurement . Sleep efficiency is calculated as the number of hours asleep divided by the number of hours in bed with the intention to sleep.
BEF-SHI Total Number of Negative Sleep Hygiene BehaviorsBaseline (T1) and Post-Intervention (T2) - 8 WeeksTotal Number of negative sleep hygiene indicators from the BEFSHI - Bedtime Environmental Features and Sleep Hygiene Index (e.g., nighttime caffeine, nighttime snacking-sugar, nicotine, excessive alcohol, excessive daytime napping, television, tablet and computer use in bedroom after 9 pm etc.) Participants are asked to respond yes (1) or no (0) to a series of sleep hygiene behaviors considered detrimental to sleep. Scores are summed. Possible scores range from 0-8 with a greater score indicating a greater number of negative sleep hygiene behaviors endorsed.

Countries

United States

Participant flow

Recruitment details

Recruitment for the intervention occurred between 2014 and 2016. Participants were recruited from the Geriatrics Clinic, the CVNR Caregiver Registry and by referrals from Social Workers and Primary Care.

Pre-assignment details

Participants were excluded from the study if both members of the dyad reported sleeping well (no sleep problems, high sleep quality) during baseline interview and/or had sleep efficiency of 85% or greater as measured by actigraphy during baseline week. Randomization occurred following baseline. Consented=102; Randomization=96.

Participants by arm

ArmCount
SLEEP-E Dyads Intervention
SLEEP-E Dyads Six-Week Tele-Health Intervention 1. . Daily core video modules on sleep education, sleep hygiene and behavioral and environmental factors influencing sleep. 2. . Daily and on-demand video modules designed to promote and provide guided instruction for daily Move Out time consisting of activity enhancement and exercise. 3. . Daily and on-demand video modules designed to promote and provide guided instruction for daily Stand Down time (meditation, therapeutic breathing and self-care). 4. . SLEEP-E Dyads book 5. . Two tele-video conferences to discuss evaluation results, obtain buy-in for the prescribed intervention and address dysfunctional beliefs and attitudes about sleep. The second call involves checking-in, encouragement, reinforcement and coaching SLEEP-E Dyads Intervention: Described in arm/group description
60
Usual Care Group
During the intervention period there is no data collection or contact with research staff other than for scheduling outcomes visits.
36
Total96

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyCaregiver (CG) Health02
Overall StudyCarepartner (CP) Health42
Overall StudyLost to Follow-up22
Overall StudyWithdrawal by Subject22

Baseline characteristics

CharacteristicSLEEP-E Dyads InterventionUsual Care GroupTotal
Age, Continuous70.12 Years
STANDARD_DEVIATION 8.14
70.11 Years
STANDARD_DEVIATION 9.43
70.12 Years
STANDARD_DEVIATION 8.61
Region of Enrollment
United States
60 Participants36 Participants96 Participants
Sex: Female, Male
Female
30 Participants18 Participants48 Participants
Sex: Female, Male
Male
30 Participants18 Participants48 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 600 / 36
other
Total, other adverse events
0 / 600 / 36
serious
Total, serious adverse events
0 / 600 / 36

Outcome results

Primary

Subjective Sleep Quality

Pittsburgh Sleep Quality Index Scores (PSQI) The Pittsburgh Sleep Quality Index is a standardized and validated measure of subjective sleep quality and sleep disturbance. The inventory has 18-items. PSQI scores range from 0 - 21. A total score \> 5 (some evidence for 8) is indicative of poor sleep quality.

Time frame: Baseline (T1) and Post-Intervention (T2) - 8 Weeks

ArmMeasureGroupValue (MEAN)Dispersion
SLEEP-E Dyads InterventionSubjective Sleep QualityBaseline8.41 units on a scaleStandard Deviation 3.64
SLEEP-E Dyads InterventionSubjective Sleep QualityPost Intervention5.98 units on a scaleStandard Deviation 2.84
Wait List Control GroupSubjective Sleep QualityBaseline8.31 units on a scaleStandard Deviation 4.03
Wait List Control GroupSubjective Sleep QualityPost Intervention8.63 units on a scaleStandard Deviation 4.19
p-value: <0.001ANOVA
Secondary

BEF-SHI Total Number of Negative Sleep Hygiene Behaviors

Total Number of negative sleep hygiene indicators from the BEFSHI - Bedtime Environmental Features and Sleep Hygiene Index (e.g., nighttime caffeine, nighttime snacking-sugar, nicotine, excessive alcohol, excessive daytime napping, television, tablet and computer use in bedroom after 9 pm etc.) Participants are asked to respond yes (1) or no (0) to a series of sleep hygiene behaviors considered detrimental to sleep. Scores are summed. Possible scores range from 0-8 with a greater score indicating a greater number of negative sleep hygiene behaviors endorsed.

Time frame: Baseline (T1) and Post-Intervention (T2) - 8 Weeks

ArmMeasureGroupValue (MEAN)Dispersion
SLEEP-E Dyads InterventionBEF-SHI Total Number of Negative Sleep Hygiene BehaviorsBaseline5.27 units on a scaleStandard Deviation 2.21
SLEEP-E Dyads InterventionBEF-SHI Total Number of Negative Sleep Hygiene BehaviorsPost Intervention3.12 units on a scaleStandard Deviation 2.08
Wait List Control GroupBEF-SHI Total Number of Negative Sleep Hygiene BehaviorsPost Intervention4.51 units on a scaleStandard Deviation 2.12
Wait List Control GroupBEF-SHI Total Number of Negative Sleep Hygiene BehaviorsBaseline4.39 units on a scaleStandard Deviation 2.27
p-value: <0.05ANOVA
Secondary

Mean Sleep Efficiency

Average sleep efficiency over 7 nights of actigraphic measurement . Sleep efficiency is calculated as the number of hours asleep divided by the number of hours in bed with the intention to sleep.

Time frame: Baseline (T1) and Post-Intervention (T2) - 8 Weeks

ArmMeasureGroupValue (MEAN)Dispersion
SLEEP-E Dyads InterventionMean Sleep EfficiencyPost Intervention81.64 percentage of sleep/time in bedStandard Deviation 7.26
SLEEP-E Dyads InterventionMean Sleep EfficiencyBaseline82.19 percentage of sleep/time in bedStandard Deviation 6.71
Wait List Control GroupMean Sleep EfficiencyBaseline82.55 percentage of sleep/time in bedStandard Deviation 5.71
Wait List Control GroupMean Sleep EfficiencyPost Intervention82.09 percentage of sleep/time in bedStandard Deviation 6.11
p-value: >0.05ANOVA

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026