RECRUITING Not applicable ClinicalTrials.gov

The Effectiveness of Guided Written Exposure Therapy for Complex PTSD in Adolescents

Sponsor: Peking University • ClinicalTrials.gov ID: NCT07325734

Registry updated: 2026-09-02

Recruiting for Similar Conditions?

Sponsors are looking for patients like you. See if you qualify for compensated research studies.

Description

This study aims to examine the effectiveness of group Guided Written Exposure Therapy for Complex Post-Traumatic Stress Disorder (GWE-C) among Chinese adolescents through a randomized controlled trial. A total of 120 participants will be recruited, with 60 randomized to the GWE-C group and 60 randomized to the supportive therapy (ST) group. The GWE-C intervention will consist of 7 to 10 group sessions. The primary outcome, assessed by the International Trauma Questionnaire (ITQ), will be measured at baseline, post-treatment, 1-month follow-up, and 3-month follow-up.

Interventions

Group Guided Written Exposure Therapy for CPTSD (GWE-C) (Behavioral)
Group Guided Written Exposure Therapy for CPTSD (GWE-C) is a manualized, exposure-based therapeutic program consisting of 7 to 10 sequential sessions. The intervention follows a structured sequence of trauma processing that addresses trauma details, associated emotions, cognitions, and impacts. Writing tasks incorporate imagery dialogues, self-compassion exercises, and resource identification to help participants alleviate C-PTSD symptoms. The interval between two consecutive sessions ranges from 0 to 2 days, with participants expected to complete all sessions within 1 to 2 weeks. The first and last sessions are scheduled to last 1.5 hours each, while the intermediate sessions are 60 minutes in duration. Each group will consist of 6 to 10 participants and will be facilitated by one counselor and one assistant.
Supportive Group (Behavioral)
Supportive group, the comparator intervention, is a non-trauma-focused treatment based on the Rogerian psychotherapy model and has been used as an active comparator in previous trials of trauma-focused therapies. The program comprises seven sessions: the first two employ group activities such as card games and interactive drawing to build a sense of belonging; sessions three to six focus on stress management and emotion regulation skills through methods including expressive drawing, relaxation training, and resource identification; the final session emphasizes reflection and sharing. Throughout, counsellors provide supportive guidance to encourage emotional expression, mutual listening, and peer support, while discussions deliberately exclude participants' individual traumatic experiences.

Eligibility criteria

Inclusion Criteria: 1. Aged between 10 and 18 years; 2. Meet the diagnostic or subclinical criteria for Complex PTSD (C-PTSD), defined as missing at most one symptom from either the PTSD or DSO clusters; 3. Possess sufficient literacy and language skills to complete writing-based tasks; 4. Be able to understand the study procedures and complete the required assessments; 5. Provide written informed consent, with consent also obtained from their legal guardians. Exclusion Criteria: 1. Presence of a severe psychiatric disorder or neurodevelopmental disorder, such as schizophrenia, bipolar I disorder, autism spectrum disorder, intellectual disability, or other severe psychiatric conditions that would interfere with study participation; 2. Presence of a severe physical illness that would impair the ability to engage in the intervention; 3. Assessed as being at high suicidal risk (e.g., current suicidal ideation with intent or plan, recent suicide attempt within the past 12 months, or severe self-harm behaviors); 4. Ongoing exposure to traumatic events; 5. Currently receiving other trauma-focused psychological treatments.

Conditions

CPTSD, Compelx Post-traumatic Stress Disorder

Locations

Changchun middle school — Fuyang, Anhui, China
Peking University — Beijing, Beijing Municipality, China
Ulanhot No. 1 High School — Ulanhot, Inner Mongolia, China
Urumqi No. 74 Middle School — Ürümqi, Xinjiang, China

Partner with Nurenyx

Showcase your study to thousands of motivated patients matching your criteria.

Learn More

Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record

Accelerate Your Clinical Trial Recruitment