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Affective Cognitive Behavioral Therapy in Persons with Somatization Disorder

Effectiveness of Affective Cognitive Behavioral Therapy in treating Persons with Somatization Disorder: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049913
Enrollment
34
Registered
2023-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: F450- Somatization disorder

Interventions

Intervention1: Affective Cognitive Behavioral Therapy to Experimental Group: The first phase is skill-focused (training patients in relaxation and behavioral management). These initial sessions are de

Sponsors

Rini Gogoi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants who fulfilling the ICD-10 criteria for Somatization disorder 2. Married and both gender 3. Aged 21-50 years. 4. Those who are high school passed and receiving treatment from LGBRIMH with 2 years of illness and are willing to give written consent.

Exclusion criteria

Exclusion criteria: 1. Participants should not be diagnosed with any severe mental disorder, co-morbid psychiatric illness (Epilepsy, Intellectual disability, Organic disorder). 2. Those who reported having other major physical medical conditions and surgery, pregnant or breastfeeding women, and that reported domestic violence, alcohol, and drug use excluding tobacco. 3. Those that will be assessed clinically with suicidal ideation at the time involved in the study will be excluded.

Design outcomes

Primary

MeasureTime frame
Affective Cognitive Behavioural Therapy (ACBT) in treating persons with Somatization disorder will help to increase patients vocational, social, and self-care activities and improve their mood and physical robustness.Timepoint: The primary outcome measure will be assessed after 1 month and 3 months post intervention.

Secondary

MeasureTime frame
The involvement of significant others and family members will help in modifying interpersonal and environmental contingencies that contribute to the maintenance of illness.Timepoint: The secondary outcome measure will be assessed after 1 month and 3 months post-intervention.

Countries

India

Contacts

Public ContactRINI GOGOI

Gauhati University

soniadeuri28@gmail.com9435080843

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026