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NCT05864469Completed

A Psychosocial Dyadic Programme for Patients With Heart Failure and Their Family Caregivers

The Effects of a Psychosocial Dyadic Intervention on the Mutuality, Psychological and Quality of Life Outcomes of Patients With Heart Failure and Their Family Caregivers: A Mixed-methods Study

Source: ClinicalTrials.gov · Last updated 24 Sept 2025

Brief summary (registry, in English)

The overall aim of the study is to evaluate the effects of a psychosocial dyadic intervention on mutuality, psychological strengths (i.e., resilience and self-compassion), psychological distress (i.e., anxiety and depression), and QoL outcomes of HF patients and caregivers. The HF patient-caregiver dyads will be randomly allocated to the intervention group to receive a 12-week relationship-focused psychosocial dyadic intervention, or to the control group to receive the usual care provided by the clinical team in the hospital.

Status (registry)
Completed
Study type
Interventional
Enrollment
192 (actual)
First submitted
9 May 2023
Start date
30 May 2023
Primary completion date
2 Feb 2025
Lead sponsor
The University of Hong Kong
NCT number
NCT05864469

What you commit to

  • Study type: Interventional
  • Participants enrolled: 192
  • From 30 May 2023 to the primary completion date, 2 Feb 2025
  • 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 illness

  • psychiatric problems requiring active treatment
  • other terminal illnesses, such as advanced cancer
  • with mechanical circulatory support, on the heart transplant list or with a history of heart transplant

Who the study is looking for

  • patients and caregivers aged 18 years or older
  • patients diagnosed with heart failure
  • able to identify one family caregiver who provides unpaid daily caregiving≥3.5hr/ day to participate
  • patients and caregivers able to read simplified Chinese and communicate in Mandarin
  • have access to a telephone at home.

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
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Coordinator of this site? Confirm its status
WuhanChinaUnknown status

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