Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
NCT07305415

Integrative Therapeutic Programme to Regulate Expressed Emotions Among Informal Caregivers of People With Dementia

Led by The University of Hong Kong · Updated on 2026-03-31

56

Participants Needed

1

Research Sites

66 weeks

Total Duration

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AI-Summary

What this Trial Is About

The dual-modal (face-to-face and online approaches), client-customized Caregivers Of dementia Processing Emotions (COPE) programme aims to 1. reduce caregivers' Expressed Emotion (EE), 2. reduce caregivers' depressive symptoms, 3. reduce the behaviourally interactive social dynamic of maladaptation (i.e., dysfunctional dyadic relationship and quality of care), and 4. improve caregivers' perceived stress from PwD's Behavioral and Psychological Symptoms of Dementia (BPSD). Researchers will compare COPE to a control group (standard therapy) to examine how effective the COPE programme is. Participants will take part in: Pretest prior to COPE implementation Post-test after COPE completion Follow up test in 3 months after COPE completion

CONDITIONS

Official Title

Integrative Therapeutic Programme to Regulate Expressed Emotions Among Informal Caregivers of People With Dementia

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a high level of expressed emotion indicated by a Family Attitude Scale (Chinese version) score of 35 or above
  • Provide care for a person with dementia for at least 4 hours per day
  • Consent to participate in the study
  • Have no acute psychiatric illness
Not Eligible

You will not qualify if you...

  • Have a Family Attitude Scale (Chinese version) score below 35
  • Provide care for a person with dementia for 4 hours or less per day
  • Do not consent to participate in the study
  • Have an acute psychiatric illness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Hong Kong

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

Y

YU Sau Fung, RN, PhD, FHKAN, FAAN, FGSA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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