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Art-integrated Rational Emotive Behaviour Education Program to Promote Mental Health of Transgender Persons

Art-integrated Rational Emotive Behaviour Education Program to Promote Mental Health of Transgender Persons: A Feasibility Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103824
Enrollment
26
Registered
2026-02-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

None listed

Interventions

Intervention1: Art integrated rational emotive behaviour education group: The group that receives REB education sessions incorporated with Art exercises will be considered as an intervention group. Th

Sponsors

University Grants Commission (UGC)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Individuals who self-identify with transgender identity (transwomen, transmen). 2. Those who have completed the age of 18 and above. 3. Patients who can read, write, and speak Tamil, or English.

Exclusion criteria

Exclusion criteria: Individuals who have been diagnosed with any psychiatric disorder. Details related to the history of severe mental disorders will be obtained through self-reporting statements.

Design outcomes

Primary

MeasureTime frame
1. Understanding the feasibility of conducting a randomized controlled trial with transgender persons 2. Development of an art-integrated Rational Emotive Behaviour Education program for transgender personsTimepoint: Time-point 1 - Pre-test (1 week before the intervention) Time-point 2 - Post-test (after the last session of the intervention) Time-point 3 - Follow-up (1 month from the date of completion of the intervention) Time-point 4 - Follow-up (3 months from the date of completion of the intervention)

Secondary

MeasureTime frame
1. Self-compassion 2. Rational Beliefs 3. Resilience 4. Psychological distressTimepoint: Time-point 1 - Pre-test (1 week before the intervention) Time-point 2 - Post-test (after the last session of the intervention) Time-point 3 - Follow-up (1 month from the date of completion of the intervention) Time-point 4 - Follow-up (3 months from the date of completion of the intervention)

Countries

India

Contacts

Public ContactSridhar R

National Institute of Mental Health and Neuro Sciences

kanmani.raju@gmail.com9945453602

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026