Actively Recruiting

Phase Not Applicable
Age: 9Years - 17Years
All Genders
ID05608551

Effects of a Psychotherapy Group Program for Children and Adolescents With Post-traumatic Stress Symptoms

Led by University of Basel · Updated on 2024-07-19

80

Participants Needed

2

Research Sites

134 weeks

Total Duration

On this page

Sponsors

U

University of Basel

Lead Sponsor

U

University of Zurich

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how including animals in trauma-focused group therapy affects the motivation of children and adolescents who have experienced post-traumatic stress. The study involves 80 young participants aged 9 to 17 years who have gone through at least one traumatic event resulting in symptoms of post-traumatic stress. The goal is to see if animal-assisted therapy can help these young people attend therapy more regularly, stay motivated, and complete their treatment successfully. Participants are randomly assigned to one of two groups: one group receives animal-assisted trauma-focused therapy (AA TF-CBT), which includes animals as part of the therapy sessions based on a structured manual, while the other group receives standard trauma-focused therapy (TF-CBT) without animals, also following a structured approach. Both therapies last for 10 weeks, and alongside these sessions, parents or guardians join three meetings to support the process. During the study, children's therapy motivation is measured before treatment, after the 10 weeks of therapy, and four weeks later to track changes over time. Researchers also assess therapeutic alliance, PTSD symptoms, self-efficacy, and quality of life at these same points. Participants will share their experiences of the group therapy during a follow-up four weeks after treatment. The study includes regular questionnaires and evaluations to monitor progress and outcomes throughout the trial period.

CONDITIONS

Brief Title

Animal-assisted Trauma-focused Therapy for Children and Adolescents

Who Can Participate

Age: 9Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 9 and 17 years
  • Experienced at least one traumatic event
  • Remembers at least one traumatic event
  • Has posttraumatic stress symptoms with a CATS-2 score of 21 or higher (participant or caregiver assessed)
  • Basic knowledge of German for child and parent to understand sessions and complete questionnaires
  • Informed consent given by legal guardian for participants younger than 14 years
  • Positive or neutral attitude towards animals
Not Eligible

You will not qualify if you...

  • Unable to complete questionnaires due to language difficulties or cognitive impairment
  • Diagnosed autism spectrum disorder that limits interaction or group participation
  • Significant safety concerns such as active suicidal thoughts or acute psychosis
  • Known substance abuse for emotion regulation (e.g., cannabis, alcohol, hard drugs)
  • Fear of domestic animals
  • Allergic reactions to domestic animals
  • History of aggressive behavior towards animals

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 10 weeks

Participants undergo a 10-week group therapy program, either animal-assisted trauma-focused therapy or standard trauma-focused therapy.

Weekly visits for up to 10 weeks

Follow-up

Duration - 4 weeks

Participants are assessed four weeks after treatment to evaluate therapy motivation, therapeutic alliance, PTSD symptoms, self-efficacy, quality of life, and perception of the group therapy.

1 follow-up visit (in-person)

Trial Site Locations

Total: 2 locations

1

University of Basel

Basel, Switzerland

Actively Recruiting

2

Psychiatrische Universitätsklinik Zürich

Zurich, Switzerland

Actively Recruiting

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Research Team

K

Karin Hediger, Prof. Dr.

W

Wanda Arnskötter, MSc.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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