Sleep Health Enhancement in Older Adults to Address Frailty
Purpose
The objective of the proposed study is to tailor a sleep health enhancement intervention to older adults and assess preliminary efficacy on reducing frailty in older adults. This pilot study will be conducted in two stages. In the treatment development stage, we will recruit n=10 older individuals age ≥65 with poor sleep health (≤ 7 on the Ru-SATED self-report questionnaire) to assess acceptability and tailor the sleep health enhancement intervention for older adults. In the pilot study stage to assess preliminary efficacy of the tailored sleep health enhancement intervention, n=30 older adults with poor sleep health will be randomly assigned to a 4-week 1x/week, telehealth-delivered sleep health enhancement intervention or to a wait-list control condition. Participants will wear wrist-worn actigraphy, complete sleep, frailty, and quality of life questionnaires at baseline and reassessments.
Condition
- Frailty
Eligibility
- Eligible Ages
- Over 65 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- ≥65 years old - ≤ 7 on the RU-SATED self-report questionnaire - MMSE ≥25 and AD8 <3
Exclusion Criteria
- Known untreated sleep disorder (such as sleep apnea or restless leg syndrome) - >3 on the STOP BANG indicating increased risk of sleep apnea - Evidence of restless legs syndrome on RLS-Diagnosis Index - Evidence of circadian rhythm sleep-wake disorder - Evidence of parasomnia - Regular use (>2x/week) of prescription or over-the-counter medications to improve sleep - Score of ≥15 on the Patient Health Questionnaire (PHQ-9) indicating severe depression or endorse any suicidal ideation (answer 1, 2 or 3 on #9 of the PHQ-9) - Score of ≥10 on the Generalized Anxiety Disorder (GAD-7) indicating moderate to severe anxiety - Self-report of current or history (up to 2 years) of drug or alcohol abuse based on the DSM-V criteria - History of nervous system disorder such as stroke or Parkinson's disease - Severe mental illness such as schizophrenia or bipolar disorder - Current or history (within 5 years) of shift work including hours of midnight-4am - Is currently receiving a behavioral sleep health intervention
Study Design
- Phase
- Phase 1
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Sleep Health Enhancement Intervention |
The sleep health enhancement intervention is a 4-week, 1x/week one-one-one program with a graduate research assistant who will be trained and supervised by the PI in provision of the sleep health enhancement intervention. |
|
|
No Intervention Wait-List Control Group |
The wait-list control group will be encouraged to continue with their usual activities and sleep habits during the wait period between baseline and reassessment and will undergo the sleep health enhancement intervention following the initial reassessment. |
|
Recruiting Locations
Kansas City, Kansas 66160
More Details
- Status
- Recruiting
- Sponsor
- University of Kansas Medical Center