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Effectiveness of Eye Movement Desensitization and Reprocessing(EMDR) plus Exposure / Response Prevention(ERP) in the treatment of OCD symptoms.

Effectiveness of Eye Movement Desensitization and Reprocessing(EMDR) plus Exposure / Response Prevention(ERP) in reducing obsessive-compulsive disorder symptoms associated with stressful life experiences: A randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190319043090N3
Enrollment
60
Registered
2020-01-18
Start date
2018-02-09
Completion date
Unknown
Last updated
2020-02-24

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 1: Experimental group with pre / post test and follow-up :Implementation of the Eye Movement Desensitization and Reprocessing in combination with Exposure / Response

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The primary diagnosis of Obsessive-Compulsive Disorder (OCD) is according to the Diagnostic and Statistical Manual of Mental Disorders(DSM-5) criteria, which will be determined by the clinical structured interview (SCID-I) Yale-Brown Obsessive-Compulsive Scale score is equal to or greater than 16 Secondary depression due to obsessive compulsive disorder Age range 18 to 60 years Minimum IQ of 80 / or minimum education in secondary school 2 / or equivalent. Existence of life-threatening or stressful experiences

Exclusion criteria

Exclusion criteria: The presence of comorbidities in either now or in the past other than depression. Substance abuse Intent to commit suicide Psychiatric disorders due to medical conditions Personality disorders Receive simultaneously any psychological treatment currently for axis I disorders Not receiving Selective Serotonin Reuptake Inhibitors(SSRI).

Design outcomes

Secondary

MeasureTime frame
Severity of symptoms of obsessive- compulsive disorder. Timepoint: Post-test after the completion of 12 sessions of therapy and 1 session follow up 3 months after the post-test stage (13 sessions in total). Method of measurement: Padua Inventory- Washington State University Revision (PI-WSUR) score.

Primary

MeasureTime frame
Severity of symptoms of obsessive- compulsive disorder. Timepoint: Pre-test pre-intervention, post-test after the completion of 12 sessions of therapy, 1 session for follow up 3 months after the post-test stage(13 sessions in total). Method of measurement: Padua Inventory- Washington State University Revision (PI-WSUR) score.;Obsessive-Compulsive type. Timepoint: Pre-test pre-intervention, post-test after the completion of 12 sessions of therapy, follow up 3 months after the post-test stage(13 sessions in total). Method of measurement: Type of obsessive-compulsive disorder according to Padua's Inventory- Washington State University Revision (PI-WSUR).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Ebrahim Sarichloo

University of social welfare and rehabilitation sciences

mesarichloo@yahoo.com+98 28 3355 5054

Outcome results

None listed

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