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The effectiveness of personalized computerized inhibitory training program (P-CIT) with Exposure and Response Prevention on obsessive-compulsive disorder

The effectiveness of personalized computerized inhibitory training program (P-CIT) with Exposure and Response Prevention on the outcome of therapy in Patients with Contamination Obsessive-Compulsive Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211027052887N1
Enrollment
30
Registered
2021-10-31
Start date
2021-11-06
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

Obsessive-compulsive disorder. Obsessive-compulsive disorder

Interventions

Intervention 1: Intervention group: personalized computerized inhibitory training program (P-CIT) with exposure and response prevention (ERP): First, participants complete the research questionnaires

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Initial diagnosis of obsessive-compulsive disorder (OCD) by a psychiatrist and then obtaining a score of 16 or higher on the Yale-Brown Obsessive-Compulsive Disorder Scale (YBOCS) Having insight so that the patient is aware of the problems and illness and also has a non-insane understanding of the cause and meaning of her illness. Familiarity with computers and email and how to work with them Age between 18 to 55 years’ old and At least Diploma education

Exclusion criteria

Exclusion criteria: Receiving psychological and pharmacological treatments for 3 months before entering the study (in the case of patients treated with psychiatric drugs if the dose of the drug in them is stable 6 weeks before the study and remains at the same dose during the study from Study will not be deleted). Concurrent psychiatric disorders such as bipolar disorder and related disorders, schizophrenia spectrum disorders and other psychotic disorders, addictive disorders and substance-related disorders (In the case of other mental disorders, patients will not be excluded from the study if the symptoms of OCD are more severe and harmful than the symptoms of the accompanying mental disorder). Having vision problems that can not be treated with medical treatment or prescription glasses. Having hearing problems that can not be treated with medical treatment or hearing aids. Having serious thoughts of active suicide Organic brain disorder based on family and patient reports

Design outcomes

Primary

MeasureTime frame
Severity of signs and symptoms in patients with obsessive-compulsive disorder. Timepoint: before the intervention, last session, 2 months after the intervention. Method of measurement: Yale-brown obsessive compulsive scale.

Secondary

MeasureTime frame
Quality of Life. Timepoint: before the intervention, last session, 2months after intervention. Method of measurement: World Health Organization's Quality of Life Questionnaire (WHOQOL-BREF).;Task control. Timepoint: before the intervention, last session, 2months after intervention. Method of measurement: Stroop.;Anxiety, depression, stress. Timepoint: before the intervention, last session, 2months after intervention. Method of measurement: Depression Anxiety and Stress Scales.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactfatemeh jafarian dehkordi

Iran University of Medical Sciences

fatemehjafarian1112@gmail.com+98 21 6655 1655

Outcome results

None listed

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