Actively Recruiting
Improving Sleep Health Outcomes for Family Caregivers
Led by Case Western Reserve University · Updated on 2026-04-07
30
Participants Needed
1
Research Sites
74 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This pilot study is intended to evaluate the feasibility, acceptability, and preliminary efficacy of an adapted sleep health intervention for family caregivers. The researchers are piloting a randomized clinical trial to test the Family Caregiver Transdiagnostic Intervention for Sleep and Circadian Dysfunction (Caregiver TranS-C), a tailored intervention that integrates cognitive behavioral therapy, mindfulness, and caregiving guidance. The caregiving-tailored adaptation of the Transdiagnostic Intervention for Sleep and Circadian Dysfunction (TranS-C) has the potential to improve sleep health outcomes and enhance psychological well-being in family caregivers.
CONDITIONS
Official Title
Improving Sleep Health Outcomes for Family Caregivers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age �318 years
- Assist a community-dwelling adult relative or friend with chronic health conditions and have been in this caregiving role for at least 6 months
- Live with the care recipient
- Have a self-reported sleep problem evidenced by one of the following criteria:
- a raw score �325 (T-score �355.3) on the PROMIS-Sleep Disturbance Short Form 8b measure, or
- self-reported suboptimal sleep health on at least one of the sleep health dimensions (regularity, satisfaction, alertness, timing, efficiency, and duration)
- Able to speak, read, and understand English
You will not qualify if you...
- Caring for an adult with a terminal illness or enrolled in hospice
- Night shift or rotational-shift worker
- Current pregnancy
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Case Western Reserve University
Cleveland, Ohio, United States, 44106
Actively Recruiting
Research Team
E
Elliane Irani, PhD, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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