Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
NCT07105345

Exploring Efficacy of Multi-Mode Cognitive Processing Therapy (CPT) for PTSD

Led by Far Eastern Memorial Hospital · Updated on 2026-03-20

60

Participants Needed

2

Research Sites

121 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a longitudinal, multicenter, single-blind, two-arm randomized controlled trial designed to evaluate the effectiveness of Multi-Modal Cognitive Processing Therapy (MMCPT) for individuals with posttraumatic stress disorder (PTSD). Participants will be randomly assigned to either the intervention group receiving MMCPT or a control group receiving treatment-as-usual (TAU). The intervention follows the standard CPT manual developed by Resick and consists of twelve weekly 90-minute individual sessions. The primary outcomes include PTSD symptom severity assessed by the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) and the PTSD Checklist for DSM-5 (PCL-5). Secondary outcomes include sleep quality (actigraphy, PSQI), anxiety (STAI), depression (HDRS-17), remission rate, and posttraumatic growth (PTGI). Assessments will occur at baseline, mid-treatment, post-treatment, and at 3-, 6-, 9-, and 12-month follow-ups.

CONDITIONS

Official Title

Exploring Efficacy of Multi-Mode Cognitive Processing Therapy (CPT) for PTSD

Who Can Participate

Age: 20Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged between 20 and 65 years
  • Diagnosed with PTSD according to DSM-5 criteria
  • Score 233 on the PTSD Checklist for DSM-5 (PCL-5)
  • Able to provide informed consent
  • Stable psychiatric medication regimen (if any) for at least 4 weeks prior to enrollment
Not Eligible

You will not qualify if you...

  • Diagnosed with schizophrenia, schizoaffective disorder, or bipolar I disorder
  • Current substance dependence or abuse within the past 6 months
  • Severe suicidal ideation or suicide attempt in the past 6 months
  • Cognitive impairment or neurological disorder affecting participation
  • Concurrent participation in other psychological treatment for PTSD

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Far Eastern Memorial Hospital

New Taipei City, Banqiao District, Taiwan, 220

Not Yet Recruiting

2

Far Eastern Memorial Hospital

New Taipei City, Banqiao District, Taiwan, 220

Actively Recruiting

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Research Team

H

Hsin-I Liu, PhD, RN

CONTACT

P

Pei-Chuan Wu, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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