Group cognitive stimulation for care-home residents with dementia or mild cognitive impairment

Effectiveness of Cognitive Stimulation Therapy Group for Residential Home Residents With Dementia and Mild Cognitive Impairment-- A Randomized Controlled Trial

Not applicable Interventional City University of Hong Kong · NCT07372066

This project will test whether a 14‑session group cognitive stimulation therapy helps older care‑home residents with dementia or mild cognitive impairment improve thinking, mood, activity, social engagement, and quality of life compared with a calligraphy activity.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment110 (estimated)
Ages60 Years and up
SexAll
SponsorCity University of Hong Kong Academic / other
Locations1 site (Hong Kong, Hong Kong)
Trial IDNCT07372066 on ClinicalTrials.gov

What this trial studies

This multicenter, cluster‑randomized trial enrolls about 110 residents from SAGE old age homes in Hong Kong and randomizes activity groups to either a 14‑session Cognitive Stimulation Therapy (CST) group or a calligraphy control group. Outcomes including standardized measures of cognitive function, depressive symptoms, activity engagement, social functioning, and quality of life will be measured before, after, and at 3‑month follow‑up by blinded research staff. The study also tests whether increases in engagement during groups predict cognitive improvement. Groups are allocated 1:1 and assessments use validated instruments such as the MoCA‑5 minute screening for undiagnosed participants.

Who should consider this trial

Good fit: Ideal candidates are residents aged 60 or older with a DSM‑5‑TR diagnosis of mild cognitive impairment or dementia who can participate independently in group activities and live in participating SAGE residential homes.

Not a fit: People with severe sensory impairments, disruptive behavior, major physical illnesses that require frequent hospitalization, or who cannot participate independently in group activities are unlikely to benefit and are excluded.

Why it matters

Potential benefit: If successful, the program could offer a low‑cost, group‑based way for care homes to improve residents' cognition, mood, engagement, social interaction, and overall quality of life.

How similar studies have performed: Prior randomized trials of group Cognitive Stimulation Therapy have reported modest, reproducible improvements in cognition and quality of life for people with dementia, though direct comparisons with activity controls in residential‑home settings are less frequently reported.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. age 60 years or older;
2. diagnosis of MCI or dementia according to the Diagnostic and Statistical Manual of Mental Disorder (Fifth edition, Text Revision).

Remark: Participants who do not receive a diagnosis of MCI or dementia will undergo a screening assessment by a researcher using the Chinese Montreal Cognitive Assessment (MoCA)-5 minutes.

Exclusion Criteria:

Those who are unable to participate independently in group activities, who exhibit disruptive behavior and/or are severely impaired by physical disabilities (e.g. severe hearing and visual impairment) and physical illnesses (e.g. frequent hospital stays) are excluded.

Where this trial is running

Hong Kong, Hong Kong

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Cognitive FunctionsCognitive Stimulation TherapyCalligraphy groupRandomized Controlled trialMild cognitive impairmentDementia
Last reviewed 2026-06-13 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.