Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Telephone-Coached Sleep Bibliotherapy for Dementia Caregivers

Official title: Telephone-Coached Sleep Bibliotherapy for Informal Caregivers of People With Dementia: A Randomized Controlled Trial

Run by The Hong Kong Polytechnic University · NCT07826663 · Data updated 2026-11-12

This study tests whether an 8-week, telephone-guided sleep self-help program helps informal caregivers of people with dementia sleep better.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment120 (estimated)
SponsorThe Hong Kong Polytechnic University
Academic / other
Locations1 site (Hung Hom, Kowloon)
StatusRecruiting
StartedAugust 1, 2026
Main results expectedDecember 2028
Study endsDecember 2028
Registry record updatedSeptember 17, 2026
Trial IDNCT07826663 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult informal caregivers (18+) living with or actively caring for a family member with dementia, reporting sleep problems, and not using sleep medications or on stable treatment for at least 6 weeks.

Probably not a fit

Caregivers with complex sleep disorders, cognitive impairment themselves, or those receiving other sleep-focused treatments may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial compares an 8-week telephone-coached sleep bibliotherapy program to a control educational booklet for informal caregivers of people with dementia. Participants are randomized to receive guided, self-directed sleep improvement materials or a booklet with weekly check-ins, in addition to usual community services. Outcomes include sleep quality, caregiving appraisal, beliefs about sleep, emotional distress, care recipient neuropsychiatric symptoms, and quality of life, assessed at baseline, after the program, and 3 months later. The primary outcome is sleep quality measured by the Pittsburgh Sleep Quality Index (PSQI). The study aims to determine if a low-cost, scalable intervention can improve caregiver sleep and well-being.

Why it matters

Potential benefit: If successful, caregivers may sleep better and experience improved well-being with a scalable, low-cost intervention.

How similar studies have gone: Prior home-based sleep interventions have shown potential in caregiver populations, but telephone-coached bibliotherapy for dementia caregivers is a relatively novel approach in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria: a) aged 18 years or older; b) provide unpaid care to a family member with dementia; c) living with the patient or actively involved in the patient's care daily for a minimum of 4 hours/day for at least 6 months; d) endorse one or more sleep problems; e) having the sleep problem with an average of 3 or more nights per week during the past month; d) taking no medication for sleep or stabilized on current medication for at least 6 weeks; e) could be contacted by phone.

Exclusion criteria: a) report a prior diagnosis of primary sleep disorder (e.g., sleep apnoea); b) have a severe chronic illness that could cause their sleep problems (e.g., emphysema); c) receive medical, psychological, or psychiatric treatment for sleep disturbance or depression; d) have cognitive impairment; e) be included in another interventional study.

Where it's running

  • The Hong Kong Polytechnic University
    Hung Hom, Kowloon, Hong Kong
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.