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NON-SUICIDAL SELF INJURY (NSSI): Exploration and Intervention

The correlation between emotional dysregulation, adult attachment, aggression orientation, and trauma symptoms with the occurrence of NSSI was explored. An intervention was applied to selective individuals engaging in NSSI. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077389
Enrollment
800
Registered
2024-11-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: R458- Other symptoms and signs involvingemotional state

Interventions

Intervention1: Trauma-Focused Cognitive Behavior Therapy: Trauma-focused cognitive behavioral therapy (TF-CBT)will address the associative cues for traumatic memory, facilitating exposure to these cue

Sponsors

ANWESHA BHATTACHARYYA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The individuals within age range of 18-24 years, Regular students studying in colleges and universities with English as the medium of instruction and communication, Students belonging to the middle socioeconomic status in Kolkata

Exclusion criteria

Exclusion criteria: Chronic physical condition like fibromyalgia, Crohn’s disease, severe diabetes or any terminal illness, traumatic brain injury or any neuropsychological injury or condition Any recent episode of any accident, sudden death of a loved one or any other source of acute psychological trauma Active suicidal ideation or intent or recent history of suicide attempt (within a month of the data collection procedure) needing emergency intervention Individuals belonging to broken homes or separated families.

Design outcomes

Primary

MeasureTime frame
NSSI occurrence, frequency and outcome were measured by FASM Depression and Anxiety symptoms were measured by BDI and BAI respectively Trauma Symptoms were measured by TSC-40Timepoint: Baseline measure was done. Intermediate measure at 6-8 weeks. Post-intervention measure at 12-16 weeks.

Secondary

MeasureTime frame
The alleviation of symptoms of depression as per BDI (at least below moderate level),and the alleviation of symptoms of anxiety as per BAI (at least below moderate level)Timepoint: 3-6 months

Countries

India

Contacts

Public ContactDr Ushri Banerjee

Department of Applied Psychology, UNIVERSITY OF CALCUTTA

ushribanerjee@gmail.com9831244000

Outcome results

None listed

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