Skip to content

Tele-group Cognitive Behavioural Family Intervention for People With Schizophrenia and Their Families (Feasibility tgCBFI)

A Randomised Controlled Study on Feasibility of Tele-group Cognitive Behavioural Family Intervention (tgCBFI) for People With Schizophrenia and Their Families

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05808244
Enrollment
24
Registered
2023-04-11
Start date
2023-06-30
Completion date
2024-09-22
Last updated
2026-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychosis, Schizophrenia

Brief summary

This mixed-method study aims to examine the feasibility of delivering tgCBFI programme to dyads of people with schizophrenia and their family caregivers, and generate preliminary evidence on the effectiveness of tgCBFI in reducing expressed emotion. The research questions are as follows. 1. What are the feasibility, acceptability, and safety of conducting a tele-group CBFI programme for people with schizophrenia and their family caregivers? 2. What effect does tgCBFI have on the expressed emotion experienced by adults with schizophrenia and the caregiving experience of their family caregivers at posttreatment and 12-week after completion of the programme? 3. What effect does tgCBFI have on the positive and negative symptoms of adults with schizophrenia and the perceived care burden and level of mood disturbance of their family caregivers at posttreatment, and 12-week after completion of the programme?

Interventions

BEHAVIORALtgCBFI

Six weekly sessions CBT-based family intervention programme

Integrated community psychiatric care with medical follow-up

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER
The University of Hong Kong
CollaboratorOTHER
Kowloon Hospital, Hong Kong
CollaboratorOTHER
Nethersole Institute of Continuing Holistic Health Education
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Service users * diagnosis of schizophrenia-spectrum disorders, based on ICD-10 made by the treating clinicians * aged 18 to 64 * able to communicate in Cantonese Family caregivers * aged 18 or above * able to communicate in Cantonese * live with service users

Exclusion criteria

Service users * have co-morbidity of learning disability, organic/neurological conditions, or substance misuse disorder * live in hostel Family caregivers -have active psychiatric conditions

Design outcomes

Primary

MeasureTime frame
Level of service satisfaction of service users and family caregiversImmediate posttreatment
Feasibility, acceptability, and safety of the programmeThroughout the whole programme

Secondary

MeasureTime frame
Perceived expressed emotion of service usersup to 12-week follow up
Positive and negative symptoms of service usersup to 12-week follow up
Mood disturbance of family caregiversup to 12-week follow up
Perceived care burden of family caregiversup to 12-week follow up
Qualitative feedback from service users and family caregiversImmediate posttreatment

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 25, 2026