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Achilles Tendon InjuryNCT06294093

Differences Between Long Distance Road Runners and Treadmill Runners in Achilles Tendon Structure

An observational study of Achilles Tendon Injury, run by University of Haifa at 1 site in Israel.

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

this study will investigate the structure of the Achilles tendon and functional tests in road runners compared to treadmill runners. Read more about this study

Who is it for?
Ages 18 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Achilles Tendon Injury
How many people
48 participants
Where
1 siteIsrael
Study dates
10 Jun 2024to 15 Aug 2025
Phase
Observational
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 18 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: healthy runners who run on a regular basis, without injuries or pain during the last 6 months

Who may be able to join

  • run regularly at least twice a week for half an hour,
  • over 80% of the training on a treadmill or road

Who cannot join

  • pain or injury to Achilles tendon during the 6 months, preventing running for at least 3 days.
  • past Achilles tendon surgeries,
  • sprained ankle in the last six months,
  • lower limb and back pain while running
  • participants who report running with minimalist shoes.

Trial locations and contacts

1 site in 1 country.

Israel1 site
  • The Academic College at Wingate

    Netanya

Other trials in Israel

About this study

Official title: Differences Between Long Distance Road Runners and Treadmill Runners in Achilles Tendon Structure, Muscle Strength, Proprioception and Balance Performance

this study will investigate the structure of the Achilles tendon and functional tests in road runners compared to treadmill runners.

Read the detailed description

Healthy runners (road and treadmill runners) who run regularly at least twice a week for half an hour, over 80% of the training on the treadmill or road, will be recruited for the study.

All subjects will fill out a demographic questionnaire for personal details (age, sex, height, weight, past injuries, training). Each participant will undergo functional tests in random order: 1. Examination of the morphology of the Achilles tendon - will be examined by ultrasound tissue characterized (UTC) 2. Balance test - Y Balance Test 3. Proprioception test - AMEDA device 4. Muscle strength test - manual dynamometer for testing gastrocnemius muscle strength. 5. Gastrocnemius muscle endurance test - single leg heel raise test until fatigue.

A comparison will be made between the two study groups.

Keywords
Achilles tendon, running

What participants receive

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

Study groups in NCT06294093
Study groupRoleWhat they receive
treadmill grouphealthy subjects who run regularly at least twice a week for half an hour, over 80% of the training on treadmill.
road grouphealthy subjects who run regularly at least twice a week for half an hour, over 80% of the training on road.

What is being measured

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

  1. ultrasound tissue characterized

    percentage of type 1,2,3,4 fibers within the tendon

    Measured: baseline

  2. Balance test

    Y Balance Test - composite score: sum of 3 reach directions in centimeters divided by 3 times the limb length then multiplied by 100

    Measured: baseline

  3. Proprioception test

    AMEDA device - scores between 0 and 1, A higher score represents better proprioception ability.

    Measured: baseline

  4. muscle strength test

    hand held dynamometer dynamometer assessment of Gastrocnemius muscle

    Measured: baseline

  5. endurance test gastrocnemius muscle

    number of single leg heel raise test until fatigue

    Measured: baseline

Timeline

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

  1. First posted5 Mar 2024
  2. Study start10 Jun 2024
  3. Primary completion15 Aug 2025
  4. Study completion15 Aug 2025

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
48 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06294093
Sponsor's protocol ID
026/24
Status last verified
Jan 2026
First submitted
27 Feb 2024
Last updated
26 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Dar G, Waddington G, Stern M, Dotan N, Steinberg N. Differences Between Long Distance Road Runners and Trail Runners in Achilles Tendon Structure and Jumping and Balance Performance. PM R. 2020 Aug;12(8):794-804. doi: 10.1002/pmrj.12296. Epub 2020 Jan 18.

    PubMed 31762215

Questions about this trial

What is this clinical trial studying?

An observational study of Achilles Tendon Injury, run by University of Haifa at 1 site in Israel.

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 2 inclusion and 5 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 26 Jan 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 Israel. 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?

ultrasound tissue characterized (time frame: baseline). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06294093, which also lists 1 linked publication.

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 26 Jan 2026.

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