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New tailored exercise program may ease stubborn achilles pain

NCT ID NCT07178418

Symptom relief Sponsor: Halic University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study tests whether a personalized exercise program based on muscle structure works better than a standard eccentric heel-drop program for people with chronic Achilles tendinopathy. Twenty adults with mid-tendon pain for at least 3 months will be randomly assigned to one of two exercise groups. Researchers will use ultrasound, strength tests, and pain questionnaires to compare changes in tendon health and physical function over time.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
exercise program
What this could lead to
If successful, this could lead to a more personalized exercise approach for Achilles tendinopathy, potentially improving recovery and reducing pain.
What could go wrong
This is a very small early-stage trial with only 20 participants, so results may not apply to everyone. Exercise programs require consistent effort, and benefits may vary.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 20 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2025

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 60 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Presence of pain and tenderness in the mid-portion of the Achilles tendon (2-6 cm proximal to the insertion) persisting for at least 3 months * Clinical diagnosis of non-insertional Achilles tendinopathy * Pain aggravated by physical activity * Palpable tenderness localized to the mid-portion of the tendon * Voluntary participation in the study with signed informed consent Exclusion Criteria: * Diagnosis of insertional Achilles tendinopathy * History of surgery or fracture in the affected lower limb within the past 12 months * Corticosteroid injection to the Achilles tendon within the past month * Presence of systemic diseases (e.g., diabetes mellitus, rheumatoid arthritis) * Presence of neurological disorders (e.g., peripheral neuropathy, central nervous system disorders) * Prior experience with eccentric exercise protocols targeting the Achilles tendon * Acute onset of symptoms suggestive of a tendon rupture

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Conditions

The condition(s) this trial relates to.

Achilles bursitis disease of the tendon

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Achilles tendinopathy (AT) Anaerobic power Balance Eccentric exercise training Isokinetic test Muscle architecture Ultrasound

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • İstanbul University

    Istanbul, Fatih, 34060, Turkey (Türkiye)

  • İstanbul University

    Istanbul, Fatih, 34060, Turkey (Türkiye)

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