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NCT07766265
NEST: A Group Intervention for Parents With Complex PTSD
Conditions: Complex Post-Traumatic Stress Disorder
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 32
Sponsor: St.Gallen University of Applied Sciences
Location: Psychiatrische Dienste Aargau (PDAG) Windisch Canton of Aargau
Summary
The goal of this pilot clinical trial is to learn whether NEST, a new trauma-informed group therapy program, is feasible and acceptable for parents with Complex PTSD, a condition that can develop after prolonged or repeated traumatic experiences. Parenting can be especially challenging for people with this condition, and few treatment programs currently address this specific need. The main questions it aims to answer are:
* Is the NEST group intervention feasible to deliver and acceptable to parents with Complex PTSD?
* Do parents' trauma-related symptoms and their experience of the parenting role change from before to after the intervention?
Participants will:
* Complete online questionnaires about trauma-related symptoms and parenting before the group therapy, after it ends, and again three months later
* Take part in nine weekly 90-minute group therapy sessions, co-led by a member of the study team and a mental health professional from the treatment site
* Some participants will additionally be invited to a short interview about their experience with the group therapy
Eligibility Criteria
Inclusion Criteria:
* Diagnosis of CPTSD according to ICD-11, confirmed by the treating psychotherapist or psychiatrist
* Caregiver of at least one child aged 0-18 years (including biological, adoptive, step-, or foster parents and other primary caregivers)
* Currently receiving individual psychotherapeutic treatment (outpatient or inpatient setting)
* Age 18 years or older
* Sufficient German language proficiency to participate in group sessions and complete study questionnaires
* Ability to provide written informed consent
Exclusion Criteria:
* Current acute psychosis or severe psychiatric instability requiring immediate intensive treatment
* Severe cognitive impairment or inability to participate adequately in group-based procedures
* No current contact with the child
* Insufficient German language proficiency
Source: ClinicalTrials.gov (NCT07766265). StuddyBuddy aggregates publicly available trial information.