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Adapting and Testing a Lifestyle Program for People with Schizophrenia and related disorders in India

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100755
Enrollment
30
Registered
2026-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: G- Mental Health

Interventions

Intervention1: Lifestyle redesign program: The Lifestyle Redesign (LSR) Program is one such structured, group-based intervention originally developed in Hong Kong. It focuses on improving participatio

Sponsors

Schizophrenia Research Foundation
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
Culturally adapted LSR program for use in Indian outpatient mental health settings for persons with Schizophrenia and related disordersTimepoint: 3 months post intervention qualitative feedback will be collected.

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDrSubhashini Gopal

Schizophrenia Research Foundation

subhashini@scarfindia.org9841474668

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026