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NCT07037550Active, not recruiting

Effectiveness of Strength-based Intervention for Elderly With Dementia Living in the Community

Effectiveness of Strength-based Intervention for Elders With Dementia Living in the Community and Residential Units: a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

In the realm of dementia care, the imperative to intervene at the earliest stages of cognitive decline is paramount. Recognizing this pivotal moment, the development of innovative and effective interventions becomes imperative in delaying dementia progression. Rooted in the Roy Adaptation Model and Zimmer's Theory of Psychological Empowerment, the investigator team has developed the empowerment-based dyadic strength-based intervention, which integrates strength-based and empowerment methodologies. Emphasizing a shift from deficits to capabilities, the strength-based approach fosters awareness of collective strengths within care dyads, facilitating coping mechanisms and resilience in the face of cognitive afflictions.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
272 (estimated)
First submitted
17 Jun 2025
Start date
1 Jul 2024
Primary completion date
28 Feb 2026
Lead sponsor
The University of Hong Kong
NCT number
NCT07037550

What you commit to

  • Study type: Interventional
  • Planned participants: 272
  • From 1 Jul 2024 to the primary completion date, 28 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • person who has communication problems with the research team

Who the study is looking for

  • age over 18
  • a confirmed diagnosis of mild dementia as indicated by the cut-off score of Montreal Cognitive Assessment-5-min at 13-18 for dementia and \>18-21 for mild cognitive impairment
  • self-reported cognitive complaints
  • have the ability to engage in the communication with the research assistant
  • able to identify a family caregiver
  • consent to participate

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Hong Kong
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.