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Achilles Tendon and Ankle Characterization in Adults With Autism

Achilles Tendon and Ankle Characterization in Adults With Autism

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07634965
Enrollment
80
Registered
2026-06-09
Start date
2026-08-10
Completion date
2027-08-01
Last updated
2026-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Disorder

Keywords

ankle, ASD, screening, Achilles tendon

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

University of Haifa
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Achilles tendonbaselineAchilles tendon structure via an ultrasound tissue characterization device

Secondary

MeasureTime frameDescription
sensory responsivenessbaselineSensory Responsiveness Questionnaire. scale from 58-290 when higher score represent increased responsiveness
ankle joint range of motionbaselinerange of motion measured by goniometer in degrees
ankle joint muscle strengthbaselineankle joint muscle strength measured by hand held dynamometer (in KgF)
toe walkingbaselineThe presence of toe walking via observation on gait (presence / absence)

Contacts

CONTACTGali Dar, PhD
gdar@univ.haifa.ac.il+972505662054

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026