Artificial Intelligence (AI)-assisted sleep interventionUsual Care
Artificial Intelligence (AI)-assisted sleep intervention: Six weeks of AI-assisted sleep intervention
Usual Care: The standard care participants receive from the healthcare system and/or their daily routines to address insomnia symptoms
Study summary
To assess the feasibility and acceptability of Artificial Intelligence (AI)-assisted sleep intervention on improving the insomnia of older adults with subjective cognitive decline.
Eligibility
Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* older adults aged ≥ 60 years
* Subjective cognitive decline questionnaire 9 (SCD-Q9) ≥ 5
* Montreal Cognitive Assessment (MoCA) ≥ 26. If the number of years of education is less than 12, one point will be added to the total score;
* with insomnia according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) and Insomnia Severity Index (ISI) ≥ 8
* reachable by phone
Exclusion Criteria:
* having a previously diagnosed primary sleep disorder, such as sleep apnoea
* suffering from a severe chronic illness that could contribute to sleep problems (e.g., emphysema)
* currently undergoing medical, psychological, or psychiatric treatment for sleep disturbances or depression
* having significant visual or hearing impairments.
Primary outcome measure(s)
Eligibility rate — Pre-intervention The number of screened participants who will be eligible.
Recruitment rate — Pre-intervention The number of participants enrolled in the study
Adherence rate — Immediately post-intervention The number of participants in the intervention and control groups who complete the intervention
Attrition rate — Immediately post-intervention The percentage of enrolled participants who discontinue participation at any point during the study.
Engagement rate — Immediately post-intervention The degree of mastery and use of the intervention content, measured by sleep diary data.
Retention rate — Immediately post-intervention The number of participants who remain in the study
Acceptability — Immediately post-intervention Participants' perceptions of and satisfaction with the intervention will be assessed through individual interviews.
Trial sites (1)
Facility
City
Region
Status
Qingyuan Second People's Hospital
Qingyuan
Guangdong
More The Hong Kong Polytechnic University trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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