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Autism Spectrum DisorderAARTNCT06025539

Animal-assisted Resilience Training for Children With Stressful Life Events or Autism Spectrum Disorder

A study testing Animal-assisted resilience training in people with Autism Spectrum Disorder and Life Change Events, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial is to learn about the effects of an animal-assisted resilience training in children who experienced stressful life events or who have a diagnosis of autism spectrum disorder. Read more about this study

Who is it for?
Ages 2 to 12 years
Conditions the study is for
Autism Spectrum Disorder, Life Change Events
What is being tested?
Animal-assisted resilience training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
107 participants
Where
1 siteSwitzerland
Study dates
10 Aug 2021to 31 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 to 12 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Age between 2 and 4 years (toddler group) or 8 and 12 years (children group)
  • History of at least one stressful life event experience OR diagnosis of autism spectrum disorder
  • Basic knowledge of either German or English of parents and child to follow the instructions during the training sessions and completion of interviews.

Who cannot join

  • Medical contraindications for contact with animals, such as allergies or phobia

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • University of Basel

    Basel, 4055

Other trials in Switzerland

About this study

Official title: Effects of an Animal-assisted Resilience Training for Children With a History of Stressful Life Events or a Diagnosis of Autism Spectrum Disorder: A Pilot Study

The goal of this clinical trial is to learn about the effects of an animal-assisted resilience training in children who experienced stressful life events or who have a diagnosis of autism spectrum disorder. The main question it aims to answer is:

  • Is an animal-assisted resilience training a feasible approach to increase resilience in children with a history of stressful life events or a diagnosis of autism spectrum disorder?

Participants will take part in 12 training sessions of a standardized resilience training. The training is group-based, takes place outdoors, and includes interactions with different animals. It focuses on self-esteem, self-perception, dealing with emotions, and social competence.

Being tested
Animal-assisted resilience training
Medical subject headings
Autism Spectrum Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Animal-assisted resilience trainingBehavioural

    Participants take part in 12 sessions (120 minutes each), each session focuses on a topic that is related to resilience. The intervention takes part outdoors on a farm, and includes interactions with several different animals. The training takes place in small groups, and includes exercises, observations, and discussions.

Study groups in NCT06025539
Study groupRoleWhat they receive
Animal-assisted resilience trainingExperimental12 sessions of group-based, animal-assisted resilience training.
Receives: Behavioral: Animal-assisted resilience training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Questionnaire on resources in childhood and adolescence

    Pre-to-post assessment changes in resilience

    Measured: 18 weeks

Secondary outcomes (5)
  1. Questionnaire to assess emotion regulation in children and adolescents

    Pre-to-post assessment changes in emotion regulation

    Measured: 18 weeks

  2. Number of attended sessions

    Number of attended sessions over the course of the training

    Measured: 12 weeks

  3. Feeling secure and motivation to participate as measured on a 0-10 scale

    Motivation and feeling secure as measured at the beginning and end of each session

    Measured: 12 weeks

  4. Intervention satisfaction as assessed in semi-structured interview

    Satisfaction with program content and structure, as measured by qualitative interview

    Measured: 18 weeks (follow-up)

  5. Strengths and Difficulties Questionnaire (SDQ)

    Pre-to-post assessment changes in peer-relationship problems and prosocial behavior measures

    Measured: 18 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Sep 2023
  2. Study start10 Aug 2021
  3. Primary completion31 Dec 2025
  4. Study completion31 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
107 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06025539
Sponsor's protocol ID
Resilience training
Acronym
AART
Status last verified
Apr 2026
First submitted
22 Aug 2023
Last updated
4 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data will be shared upon request and only once study results have been published.

Questions about this trial

What is this clinical trial studying?

A study testing Animal-assisted resilience training in people with Autism Spectrum Disorder and Life Change Events, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Questionnaire on resources in childhood and adolescence (time frame: 18 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2026.

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