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NCT07781748Not yet recruiting

Improving Quality of Informal Care for People With Schizophrenia

Improving Quality of Informal Care for Persons With Schizophrenia: A Randomized Controlled Trial of Multicomponent Dyadic Intervention

Source: ClinicalTrials.gov · Last updated 25 Aug 2026

Brief summary (registry, in English)

The goal of this clinical trial is to learn if a new support program can improve the quality of informal care for people with schizophrenia in rural China. Informal care means the unpaid care given by family members. Quality of care involves both the care that family members give and the care that people with schizophrenia receive. The study also looks at whether the program improves the health and well-being of both groups. The main questions it aims to answer are: 1. Does the support program improve the quality of care that family caregivers provide and that people with schizophrenia receive? 2. Does the program improve the health and well-being of people with schizophrenia and their caregivers? Researchers will compare three groups to see which works best: 1. A full support program with health education, physical activities, and spiritual activities 2. A program with health education only 3. A control group that receives only routine care Each person with schizophrenia takes part together with their family caregiver as a pair. Participants will: 1. Take part in an 8-week program in their community 2. Answer survey questions three times: before the program, right after it ends, and 6 months later 3. Some participants will also join interviews to share their experiences

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
228 (estimated)
First submitted
20 Aug 2026
Start date
1 Jul 2027
Primary completion date
30 Nov 2028
Lead sponsor
Chinese University of Hong Kong
NCT number
NCT07781748

What you commit to

  • Study type: Interventional
  • Planned participants: 228
  • From 1 Jul 2027 to the primary completion date, 30 Nov 2028
  • 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

  • Persons with schizophrenia (PwS): Likely to engage in risky behaviors (e.g., suicide or violence), or a history of alcohol or substance abuse; Identified by professionals as unsuitable to participate (e.g., unable to sustain meaningful conversation); Having other schizophrenia spectrum disorders or co-existing neurodevelopmental disorders
  • Informal caregivers (ICGs): Likely to engage in risky behaviors (e.g., suicide or violence); Identified by professionals as unsuitable to participate (e.g., having a mental illness or unable to understand instructions)

Who the study is looking for

  • Persons with schizophrenia (PwS): Aged 18 years or older; Diagnosed with schizophrenia by a psychiatrist, with the diagnosis validated using SCID-5; Have not previously participated in any intervention studies; Functional and able to communicate and take part in group activities; Able to provide written informed consent
  • Informal caregivers (ICGs): Aged 18 years or older; Provide unpaid care to a person with schizophrenia; Have not previously participated in any intervention studies; Able to provide written informed consent

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
Xinjin Second Peope's Hospital
Coordinator of this site? Confirm its status
ChengduChinaUnknown status

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