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Self-Harm: Tool and Intervention development for adolescents and young adults

Self-Harm in Transitional Age Youth (TAY): Development and Validation of an Assessment Tool and Randomised Feasibility Trial of a Trauma-Focused CBT Intervention Module

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072474
Enrollment
70
Registered
2024-08-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: F99- Mental disorder, not otherwise specified

Interventions

Intervention1: Trauma Focussed Cognitive Behavioral Therapy: A therapist-facilitated, CBT-based brief trauma and self-harm focused psychological intervention with individual sessions. Number of sessi

Sponsors

University Grants Commission
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosed case of specific mental illness including EUPD, Depression, Anxiety, PTSD, Adjustment disorder 2. History of experience of at least one trauma incident 3. History of self-harm- 5 incidents within last one year 4. Psychotherapy naïve 5. On/Off medication

Exclusion criteria

Exclusion criteria: 1. Known case of physical, neurological, or mental disability 2. Diagnosed case of severe mental illness including BPAD, OCD, Psychosis, MBD due to substance use in dependent pattern, neurodevelopmental disorders (ID, ASD, ADHD) 3. History of suicide attempt or para-suicide attempt in past one year 4. Unable to understand Hindi or English 5. Not consenting

Design outcomes

Primary

MeasureTime frame
Frequency and severity of self harmTimepoint: Baseline and post intervention (6-8 weeks after baseline assessment)

Secondary

MeasureTime frame
Impulsivity, emotional regulation, depression, anxiety, stress, childhood trauma, resilience, peer relationships, emotional intelligence, family functioningTimepoint: baseline & post intervention (6-8 weeks after baseline assessment)

Countries

India

Contacts

Public ContactAkanksha Yadav

All India Institute of Medical Sciences (AIIMS), New Delhi

sujatasatapathy2022@gmail.com9999267141

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026