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Clinical Trials/CTRI/2026/01/100755
CTRI/2026/01/100755
Not yet recruiting
Not Applicable

Lifestyle Redesign Program – Cultural Adaptation and Field Testing: A Formative Study

Schizophrenia Research Foundation0 sites30 target enrollmentStarted: September 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Schizophrenia Research Foundation
Enrollment
30

Overview

Brief Summary

This study is guided by the Formative Method for Adapting Psychotherapy (FMAP), a structured collaborative framework for systematically adapting interventions to enhance their cultural relevance (Hwang, 2009). 

This study aims to culturally adapt and field test the Lifestyle Redesign (LSR) program for individuals with schizophrenia and related disorders in the Indian context. The LSR program is a structured, group-based psychosocial intervention originally developed in Hong Kong, focusing on enhancing participation in daily life domains such as leisure, domestic activities, social engagement, and work.

The program consists of 10 weekly group coaching sessions, each lasting 1–2 hours, facilitated by two trained coaches. Given its original development in Hong Kong, a systematic formative cultural adaptation will be undertaken using focus group discussions with service users, caregivers, and mental health professionals to identify contextually relevant modifications. The adapted LSR program will then be field tested in a clinical setting among persons with schizophrenia. Qualitative feedback from participants and facilitators will be analysed to inform further refinement of the intervention and planning of a future randomized controlled trial.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 55.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients: with a clinical diagnosis of schizophrenia or related disorders (ICD-10), who are clinically stable, capable of providing informed consent and only those who had participated in the LSR programme at SCARF will be considered eligible.
  • Caregivers: Primary caregivers (parents, siblings, spouses, or close relatives) of individuals with schizophrenia who assume day-to-day caregiving responsibilities.
  • Caregivers unwilling to provide informed consent will be excluded.
  • Mental Health Professionals: Psychiatrists, psychologists, and social workers with at least two years of experience in working with individuals with schizophrenia and related disorders.

Exclusion Criteria

  • Patients:who are acutely unwell or have unrelated cognitive impairments will be excluded.
  • Caregivers:unwilling to provide informed consent will be excluded.
  • Mental Health Professionals: Those unwilling to provide consent will be excluded.

Investigators

Sponsor
Schizophrenia Research Foundation
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Hepsipa Omega Juliet

Schizophrenia Research Foundation

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