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To study if there is a decrease of coercive disruptive behaviour and changes in severity of obsessive and compulsive symptoms after providing integrative expsoure response prevention therapy for children and adolescents with obsessive compulsive disorder

Not Applicable
Conditions
Health Condition 1: F422- Mixed obsessional thoughts and acts
Registration Number
CTRI/2024/04/065442
Lead Sponsor
Central institute of Psychiatry Ranchi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a) Children and adolescents diagnosed with OCD as per DCR-10(1993) WHO.

b) Children and adolescents with mild to moderate severity of anxiety and depression as

measured by respective applicable tools used in the study.

c) Children and adolescents between ages 9 to less than 18 years

d) Children and adolescents obtaining Grade III Intellectual Capacity Average (25th

Percentile) and above in intelligence quotient test

e) Primary caregiver with no history or currently diagnosed with any mental illness

f) Children and adolescents giving assent and parents giving informed consent.

Exclusion Criteria

a) Children and adolescent diagnosed with other comorbid psychiatric disorders except

for caffeine and nicotine use

b) Children and adolescents diagnosed with severe depression or any major physical or

neurological disorder.

c) Children and adolescents obtaining less than the 25th percentile on Ravens SPM

d) Primary caregiver with a history or currently diagnosed with any mental illness

d) Children and adolescents not giving assent or parents not giving informed consent.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The severity of coercive disruptive behaviour, Severity of obsessive-compulsive behaviour, the severity of anxiety, the severity of depression and global impressionTimepoint: Pre-intervention (1st week), mid-intervention, post-intervention (4th week) and one-month follow-up (8th week).
Secondary Outcome Measures
NameTimeMethod
family accommodation, parental tolerance, child and adolescent distress, resilience, or family functioning scale by child and parentTimepoint: pre-intervention (at baseline) and post-test (at 4th week)
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