Actively Recruiting

Phase Not Applicable
Age: 16Years - 25Years
All Genders
NCT07238153

Promoting Emotional and Autonomic Control Through Guided Breathing Exercises for Emerging Adults With Autism

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2026-04-29

68

Participants Needed

2

Research Sites

121 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study examines the impact of guided breathing exercises on stress and heart rate variability (HRV) in autistic young adults. It explores how daily movement behavior (sleep, physical activity and sedentary behavior) influences HRV and to what extent two guided breathing exercises can affect HRV. Additionally, the study investigates how participants perceive the exercises in terms of usability and usefulness.

CONDITIONS

Official Title

Promoting Emotional and Autonomic Control Through Guided Breathing Exercises for Emerging Adults With Autism

Who Can Participate

Age: 16Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Provide voluntary written informed consent (or assent with parental consent if under 18)
  • Male or female (biological)
  • Between 16 and 25 years old
  • Diagnosed with autism as described in the DSM-IV/DSM-5(-TR)
Not Eligible

You will not qualify if you...

  • History of congenital heart disease, cardiovascular abnormalities, or somatic conditions interfering with heart rate variability or breathing exercises
  • Acute agitation or severe psychiatric symptoms (psychosis, mania, major depression) or active substance use
  • Intellectual disability with IQ below 70 as described in the DSM-IV/DSM-V
  • Insufficient Dutch language skills to follow instructions and complete questionnaires
  • Pregnant females
  • Participation in another interventional study involving investigational products or devices
  • Use of medication affecting cardiac modulation (except hormonal contraceptives)
  • Hearing or vision impairment not correctable to normal functioning

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

KU Leuven

Leuven, Vlaams Brabant, Belgium, 3000

Actively Recruiting

2

UPC Z.Org

Leuven, Belgium

Not Yet Recruiting

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Research Team

E

Esther Meers

CONTACT

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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