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A study to evaluate whether nurse-led counseling and support are effective in improving the symptoms, quality of life, daily functioning, and confidence in managing their condition for people with obsessive-compulsive disorder.

The effectiveness of a Nurse-led psychosocial intervention package on the treatment outcome, functional impairment, health-related quality of life, and self-efficacy among patients with obsessive-compulsive disorder (OCD)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080405
Enrollment
100
Registered
2025-02-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: F422- Mixed obsessional thoughts and acts

Interventions

Intervention1: Nurse-led Psychosocial interventions: Standard of Care + The psychosocial interventions include the following components a) Psychoeducation for 30 minutes, on days 1 and 2 b) Motivati

Sponsors

RAKESH V R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients With a diagnosis of OCD seeking follow-up treatment from the psychiatric department 2. Aged between 18 to 60 years 3. Receiving treatment and follow-up for OCD for at least the last 6 months 4. Having a moderate to good level of insight about the illness. 5. Able to read and understand Hindi, Odia, or English 6. Able to communicate with the researcher 7. Well-versed in using mobile phone

Exclusion criteria

Exclusion criteria: Patients who were; 1. Not willing to participate in the study/intervention 2. With comorbid psychiatric disorders and substance use disorders except for depression and anxiety 3. On any nurse led structured psychosocial intervention along with treatment as usual. 4. With compromised cognitive functions 5. With severe visual or hearing defects or any other sensory or motor problems that may inhibit the completion of nurse-led intervention 6. with an acute risk of suicide

Design outcomes

Primary

MeasureTime frame
Severity of illnessTimepoint: Baseline, 6th week, 12th week—

Secondary

MeasureTime frame
Functional impairment, health related quality of life, self efficacyTimepoint: Baseline, 6th week, 12th week—

Countries

India

Contacts

Public ContactDr Udit Kumar Panda

Kalinga Institute of Medical Sciences (KIMS), KIIT University, Bhubaneswar

uditkumar.panda@kims.ac.in7978961817

Outcome results

None listed

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