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Active Not RecruitingNCT06955845

Efficacy of Eye Movement Desensitization and Reprocessing (EMDR) Therapy Versus Selective Serotonin Reuptake Inhibitors (SSRIs) in the Treatment of Post-Traumatic Stress Disorder

Efficacy of Eye Movement Desensitization and Reprocessing (EMDR) Therapy Versus Selective Serotonin Reuptake Inhibitors (SSRIs) in the Treatment of Post-Traumatic Stress Disorder: A Randomized Controlled Trial

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Asad Ullah Jan · Other Government
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This randomized controlled trial aims to compare the efficacy of Eye Movement Desensitization and Reprocessing (EMDR) therapy versus Selective Serotonin Reuptake Inhibitors (SSRIs) in the treatment of Post-Traumatic Stress Disorder (PTSD). Adult patients diagnosed with PTSD will be randomly assigned to receive either EMDR therapy or SSRIs for a period of six weeks. The primary outcome is the rate of remission as measured by validated PTSD symptom severity scales at Week 6. Secondary outcomes include changes in functional impairment and patient-reported quality of life. The study seeks to determine whether EMDR therapy is a non-pharmacological alternative to SSRIs for achieving symptom remission in PTSD.

Conditions

Interventions

TypeNameDescription
BEHAVIORALEye Movement Desensitization and Reprocessing TherapyPatients in this arm will receive weekly EMDR sessions for 6 weeks
DRUGSelective serotonin reuptake inhibitorsThe patients will receive an SSRI medication daily for 6 weeks. The dose will be titrated by the clinician.

Timeline

Start date
2025-05-06
Primary completion
2025-11-30
Completion
2025-12-31
First posted
2025-05-02
Last updated
2025-07-09

Locations

2 sites across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06955845. Inclusion in this directory is not an endorsement.