Skip to content

Self-Management of Sleep Among Older Adults

Self-Management of Sleep Among Older Adults Using Personal Monitoring: A Feasibility Study

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03837249
Enrollment
26
Registered
2019-02-12
Start date
2019-02-04
Completion date
2020-01-30
Last updated
2020-02-26

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

Conditions

Sleep Disturbance

Keywords

Older People, Sleep Disturbance, Self-Monitoring, Self-Management, Social Support, Wrist-worn Actigraphy

Brief summary

The purpose of this study is to test the feasibility of older persons use of a personal sleep monitoring device(PSMD)to improve self-management of sleep. Disrupted sleep occurs in up to 50% of persons over the age of 65 with chronic health conditions. Impaired sleep negatively influences subjective and objective health outcomes.To improve their sleep, older adults with chronic health conditions could benefit from objective information, available through personal health monitoring devices, about their current and changing sleep patterns. Based on this information, sleep self-management interventions can be individualized and shared, and associations between sleep and health changes may be better managed.

Interventions

DEVICEPersonal Sleep Monitoring

Wearable Sleep Self-Monitoring Device (Actigraphy)

Sponsors

University of Massachusetts, Amherst
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Masking description

One group - personal sleep monitoring data with-held then provided after the intervention period.

Intervention model description

Comparative control - 3 group

Eligibility

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

Inclusion criteria

* 65 years or older * Self-report difficulty sleeping * Willingness to wear the PSMD for four weeks * Cognitive abilities (Mini Cog of 5 or above).

Exclusion criteria

* Under the age of 65 * Presence of known sleep disorders * Severe cognitive or neurosensory impairment

Design outcomes

Primary

MeasureTime frameDescription
Use of A Personal Sleep Monitoring Device (PSMD)up to 4 weeksDemonstrates use of Personal Sleep Self-Monitor through data downloads and self-report
Changes in SleepWeek 1 and Week 4Demonstrated sleep changes indicated by change in BRCS NINR PROMIS SF V1 Sleep Disturbance Scale 6a (a 6 item, 5 point likert scale with higher scores reflecting more sleep disturbance and lower scores less.
Changes in HealthWeek 1 and Week 4Demonstrated health changes indicated by change in BRCS NINR PROMIS Global Health Short Form Scale 10a (10 item, 5 point likert scale) with higher scores reflecting better health (3 items reverse scoring)

Secondary

MeasureTime frameDescription
Usability of PSMDWeek 2 and 4Demonstrated through adapted System Usability Scale Scores (10 items, 5 point likert scale) with high agreement demonstrating higher levels of satisfaction using the device

Countries

United States

Outcome results

None listed

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