Compassion-focused therapy for reducing self-criticism in complex PTSD patients
Effectiveness of Compassion Focused Therapy (CFT) for Reducing Self-criticism in Female Patients with Complex PTSD: a Single-case Experimental Study
NA · University of Twente · NCT05791760
This study is testing whether compassion-focused therapy can help people with complex PTSD feel less self-critical and improve their emotional well-being.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 15 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | University of Twente (other) |
| Locations | 1 site (Enschede, Overijssel) |
| Trial ID | NCT05791760 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of compassion-focused therapy (CFT) in reducing self-criticism among patients diagnosed with complex PTSD. It targets individuals who have experienced repeated traumatic events, particularly in interpersonal contexts, and suffer from severe self-criticism. Participants will engage in CFT and complete twice-weekly questionnaires over a 24-week period to assess changes in their self-criticism levels. The study aims to provide insights into how CFT can help improve emotional regulation and overall well-being in this population.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 65 with a diagnosis of complex PTSD and severe self-criticism.
Not a fit: Patients who do not meet the age criteria or lack sufficient Dutch language proficiency may not benefit from this study.
Why it matters
Potential benefit: If successful, this therapy could significantly reduce self-criticism and improve emotional well-being for patients with complex PTSD.
How similar studies have performed: While compassion-focused therapy is a recognized approach, this specific application for complex PTSD is relatively novel and has not been extensively tested in similar studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * The participant is between 18 and 65 years old. * Diagnosis of cPTSD and severe problems with self criticism (as diagnosed by an experienced clinican). * The participant gives consent to participate in the study using the online informed consent procedure. * Sufficient Dutch language proficiency and average intelligence. * The participant has an e-mail address and is in possession of a smartphone or tablet with access to the internet. * The participant is willing to complete twice-weekly questionnaires for up to 24 weeks. Exclusion criteria
Where this trial is running
Enschede, Overijssel
- University of Twente — Enschede, Overijssel, Netherlands (RECRUITING)
Study contacts
- Study coordinator: esther baas
- Email: e.baas01@mediant.nl
- Phone: +31534755755
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Posttraumatic Stress Disorder, PTSD, Shame, Compassion, Well-being