CTRI/2025/02/080405RecruitingNot Applicable
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)
RAKESH V R1 site in 1 country100 target enrollmentStarted: February 24, 2025Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Severity of illness
Study Overview
Brief Summary
This is a nonrandomized parallel group controlled study to assess the efficacy of add-on nurse-led psychosocial interventions on the illness severity, functional impairment, health-related quality of life, and self-efficacy among patients with obsessive-compulsive disorder. The primary outcomes are illness severity, functional impairment, health related quality of life, and self efficacy among patients with obsessive compulsive disorder. The outcomes will be ascertained at baseline as well as at the 6th week and 12th week after the nurse led psychosocial intervention.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients With a diagnosis of OCD seeking follow-up treatment from the psychiatric department
- •Aged between 18 to 60 years
- •Receiving treatment and follow-up for OCD for at least the last 6 months
- •Having a moderate to good level of insight about the illness.
- •Able to read and understand Hindi, Odia, or English
- •Able to communicate with the researcher
- •Well-versed in using mobile phone.
Exclusion Criteria
- •Patients who were;
- •Not willing to participate in the study/intervention
- •With comorbid psychiatric disorders and substance use disorders except for depression and anxiety
- •On any nurse led structured psychosocial intervention along with treatment as usual.
- •With compromised cognitive functions
- •With severe visual or hearing defects or any other sensory or motor problems that may inhibit the completion of nurse-led intervention
- •with an acute risk of suicide.
Outcomes
Primary Outcomes
Severity of illness
Time Frame: Baseline, 6th week, 12th week
Secondary Outcomes
- Functional impairment, health related quality of life, self efficacy(Baseline, 6th week, 12th week)
Investigators
RAKESH V R
All India Institute of Medical Sciences Bhubaneswar
Study Sites (1)
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