Clinical Trial

P-CRP for Recent-Onset Severe Trauma

Study acronym: P-CRP
Completed
View on ClinicalTrials.gov →
Summary
The purpose of this retrospective study was to evaluate the effectiveness of a new psychotherapy technique called Psychological Cognitive Reprocessing Procedure (P-CRP) in treating trauma symptoms. The P-CRP intervention was developed and manualized by the principal investigator (Z.B.Baydar). Participants were randomly assigned to either the P-CRP intervention group, an active control group, or a waitlist condition. The study aimed to determine if this new method, which focused on episodic buffer processing, significantly reduced trauma-related psychological distress compared to standard approaches. Data collected during the intervention phase were analyzed to assess the efficacy of the P-CRP technique.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2026-01-14; most recent amendment 2026-07-13.
Trial Details
NCT Number NCT07360990
Lead Sponsor Zahide Betül Baydar
Collaborators: Istanbul Rumeli University
Conditions Trauma and Stress Related Disorders, Grief (Traumatic Grief and Existential Grief), Stress Disorder - Post-traumatic (Acute)
Enrollment 43 participants
Start Date 2025-03-05
Primary Completion 2025-06-11 (estimated)
Study Completion 2025-07-11 (estimated)
Updated on ClinicalTrials.gov 2026-07-14