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Clinical Trials/NCT06394700
NCT06394700
Recruiting
Not Applicable

Written Exposure Therapy and App-Delivered Mindfulness-Based Meditation for PTSD and Subthreshold PTSD in China: A Pilot Randomized Controlled Trial

Peking University1 site in 1 country45 target enrollmentNovember 11, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
PTSD
Sponsor
Peking University
Enrollment
45
Locations
1
Primary Endpoint
PTSD symptom severity
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this study is to use a pilot RCT to assess the effectiveness of Written Exposure Therapy (WET) and a mindfulness-based app (MBA) for managing PTSD and comorbid insomnia in China. The main questions it aims to answer are:

  1. Does WET alone reduce PTSD symptoms in Chinese patients with PTSD and subthreshold PTSD?
  2. Does the addition of MBA to WET lead to greater reductions in comorbid insomnia symptoms compared to WET alone?

Researchers will compare WET alone and MCC to see if WET provides benefits in managing PTSD. Researchers will compare WET plus MBA and WET group to see if the integrated MBA treatment provides additional benefits in managing insomnia.

Participants will:

  • Undergo random assignment to one of three groups: WET, WET plus MBA, or MCC.
  • Receive clinical interviews for primary outcomes (PTSD symptoms) at baseline, posttreatment, and during follow-ups.
  • Provide self-reported data on PTSD symptoms and insomnia severity at multiple time points.
  • In the WET plus MBA group, additionally use a mindfulness-based app as part of their treatment.
Registry
clinicaltrials.gov
Start Date
November 11, 2021
End Date
August 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Peking University
Responsible Party
Principal Investigator
Principal Investigator

Yinyin Zang, PhD

Principal Investigator

Peking University

Eligibility Criteria

Inclusion Criteria

  • Adult male and female aged between 18-65 years old;
  • A diagnosis of PTSD or subthreshold PTSD (PTSD Symptom Scale, Interview Version for DSM-5, PSSI-5);
  • If currently taking psychotropic medication, taking a stable one for at least 4 weeks;
  • A smartphone owner and no obstacle to the Now Meditation App;
  • Scoring 12 or more on Insomnia Severity Index (ISI; the symptoms appear after the diagnosis of full/subthreshold PTSD).

Exclusion Criteria

  • A diagnosis of bipolar disorder or psychotic disorder;
  • Current substance dependence;
  • Evidence of a moderate or severe traumatic brain injury (as determined by the obstacle to comprehending the baseline screening questionnaires);
  • Serious suicidal ideation (as determined by the Scale for Suicidal Ideation);
  • Other psychiatric disorders severe enough to warrant designation as the primary disorder;
  • Taking psychotherapy for PTSD currently.

Outcomes

Primary Outcomes

PTSD symptom severity

Time Frame: Assessed at baseline, immediately post-treatment, and at 3-month follow-up periods.

The reduction in PTSD symptoms will be measured using the PTSD Symptom Scale, Interview Version for DSM-5 (PSSI-5). This clinician-administered interview assesses the frequency and severity of PTSD symptoms using a 5-point Likert scale ranging from 0 (not at all) to 4 (very much).

Secondary Outcomes

  • Insomnia Severity(Insomnia severity is assessed at baseline, weekly during the 5-week treatment period, and at the immediate post-treatment, and 3-month follow-up assessments.)

Study Sites (1)

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