Cognitive Behavioral Therapy for Insomnia delivered via instant messaging for stroke caregivers
The Effect of Instant Message-delivered Brief Cognitive Behavioural Therapy for Insomnia (CBT-I) in Stroke Family Caregivers: a Mixed Method Study
NA · The University of Hong Kong · NCT05952245
This study tests if sending Cognitive Behavioral Therapy for Insomnia through instant messaging can help caregivers of stroke survivors sleep better and feel less stressed.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 138 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | The University of Hong Kong (other) |
| Locations | 5 sites (Hong Kong and 4 other locations) |
| Trial ID | NCT05952245 on ClinicalTrials.gov |
What this trial studies
This trial evaluates the effectiveness of an instant message-delivered Cognitive Behavioral Therapy for Insomnia (CBT-I) intervention aimed at reducing insomnia symptoms among caregivers of stroke survivors. Participants will receive personalized psychological support through messaging apps over a three-month period, while a control group will receive basic education on stroke care and sleep hygiene. The study will measure outcomes such as sleep quality, depressive symptoms, and caregiver burden using validated scales. Additionally, a qualitative study will explore participants' experiences with the intervention.
Who should consider this trial
Good fit: Ideal candidates are primary family caregivers of stroke survivors who are at least 18 years old and experience clinically significant insomnia.
Not a fit: Patients who have a psychiatric diagnosis, are currently taking sleep medications, or are involved in other psychological interventions may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve sleep quality and overall well-being for stroke caregivers.
How similar studies have performed: Previous studies have shown that internet-delivered CBT-I can effectively reduce insomnia symptoms, indicating potential success for this innovative approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Primary family caregiver (Aged ≥18) of stroke survivor * Able to read and communicate in Chinese * Engaged caregiving roles for \> 4 hours per day; * Able to use a smartphone messaging app (e.g., WhatsApp and WeChat) * SCI ≤ 21 scores (i.e., clinically significant insomnia) Exclusion Criteria: * Has provided care for \<1 month prior to recruitment * Has a diagnosis of psychiatric disease or is currently taking psychotropic drugs * Currently taking medication to help with sleep * Currently participating in any type of psychological intervention
Where this trial is running
Hong Kong and 4 other locations
- Hong Kong PHAB Association — Hong Kong, Hong Kong (RECRUITING)
- Hong Kong Stroke Association — Hong Kong, Hong Kong (RECRUITING)
- NT West Community Centre — Hong Kong, Hong Kong (RECRUITING)
- Queen Mary Hospital — Hong Kong, Hong Kong (RECRUITING)
- The Hong Kong Society for Rehabilitation — Hong Kong, Hong Kong (RECRUITING)
Study contacts
- Study coordinator: Jung Jae LEE
- Email: leejay@hku.hk
- Phone: +852 3917 6971
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stroke, Insomnia, Depressive Symptoms, Caregiver Burnout, Psychological Distress, Mobile Phone Use