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A Brief Intervention for PTSD - BWRT

NCT07460817 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2026-03-10

No results posted yet for this study

Summary

The purpose of this study is to investigate if a novel brief intervention for Posttraumatic stress disorder (PTSD) is comparable to other traditional clinical interventions for symptom reduction.

Conditions

  • Post Traumatic Stress Disorder

Interventions

BEHAVIORAL

BrainWorking Recursive Therapy

one session therapy

BEHAVIORAL

Treatment as usual

evidence-based therapy

Sponsors & Collaborators

  • University of Bergen

    lead OTHER

Principal Investigators

  • Åsa Hammar, PhD · University of Bergen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-02
Primary Completion
2029-12-31
Completion
2029-12-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07460817 on ClinicalTrials.gov