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NCT Number: NCT07634965

Achilles Tendon and Ankle Characterization in Adults With Autism

This study aims to identify ankle structural and functional profiles associated with sensory responsiveness and toe walking in adults with ASD. Expected outcomes include detecting group differences between adults with ASD and matched controls and identifying associations among sensory responsiveness, toe-walking status, and objective ankle measures.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

About this study

This study aims to examine ankle musculoskeletal characteristics in adults with Autism Spectrum Disorder.

A cross-sectional, community-based comparative study will enroll 80 adults aged 18-40, including 40 adults with ASD recruited in partnership with a supported residential community and 40 age- and sex-matched controls. Participants will complete a single assessment session evaluating ankle musculoskeletal characteristics, including tendon structure using ultrasonographic tissue characterization (UTC), ankle strength and range of motion, proprioceptive discrimination using the AMEDA apparatus, and assessment of current and past toe walking, alongside quantitative evaluation of sensory responsiveness using a validated questionnaire (Sensory Responsiveness Questionnaire - SQR). Group comparisons will evaluate differences in ankle structure and function, and association analyses will evaluate relationships among sensory responsiveness, toe-walking status, and ankle measures within the ASD group. Findings will inform the identification of preliminary clinical indicators to support the development of future community-based screening and physiotherapy interventions.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • a diagnosis of ASD, or with another diagnosis that includes features of ASD (such as fragile x),
  • independent in daily activities,
  • live alone,
  • have a moderate-high level of functioning.
  • Ability to understand basic instructions for performing the tests, signing an informed consent form or having a guardian sign an informed consent form

Exclusion criteria

  • other neurological diseases (e.g., CP, multiple sclerosis),
  • significant orthopedic injuries to the lower limb in the past year,
  • previous ankle or Achilles tendon surgeries,
  • additional diseases that may affect the structure of the Achilles tendon and ankle,
  • who have not signed an informed consent form or are not interested in participating in the study

Treatment and study plan

Primary outcomes

  1. Achilles tendon

    Time frame: baseline

    Achilles tendon structure via an ultrasound tissue characterization device

Secondary outcomes

  1. sensory responsiveness

    Time frame: baseline

    Sensory Responsiveness Questionnaire. scale from 58-290 when higher score represent increased responsiveness

  2. ankle joint range of motion

    Time frame: baseline

    range of motion measured by goniometer in degrees

  3. ankle joint muscle strength

    Time frame: baseline

    ankle joint muscle strength measured by hand held dynamometer (in KgF)

  4. toe walking

    Time frame: baseline

    The presence of toe walking via observation on gait (presence / absence)

Study contacts

Contact information is provided by the study sponsor or research team.

Gali Dar, PhD

CONTACT

[email protected]

+972505662054

Sponsors and collaborators

Lead sponsor

University of Haifa

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jun 9, 2026
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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