Can a phone app replace the Doctor's exam for ankle recovery?
NCT ID NCT07197593
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study checks if a smartphone app can reliably measure calf muscle strength in people recovering from Achilles tendon rupture or ankle sprain. Researchers will compare results from 70 participants (patients and healthy controls) using the app during calf raise exercises. The goal is to see if the app provides valid and consistent measurements that could help track recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could provide a simple, reliable way for doctors to track recovery after ankle injuries using a smartphone app.
- What could go wrong
- This is an early observational study with only 70 participants, so results may not apply to everyone. The app's accuracy in real-world clinics is still unproven.
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
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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
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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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May 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
General Inclusion Criteria: * Signed informed consent * Aged 18-65 years * German or English speaking Inclusion Criteria: LAS individuals: Unilateral LAS 4-16 weeks post-injury diagnosed by a physician as LAS, supination trauma, ankle distortion or ligamentous ankle injury. ATR individuals: Unilateral ATR 6- 24 months post-injury/surgery (surgical or conservative treatment). Healthy controls: Matched to Patients by Group Level: Physical Activity, Age and Gender. Exclusion Criteria: LAS individuals: Medial Ligament injuries (Grade II or III) ATR individuals: Previous ATR General Exclusion Criteria: * Chronic Ankle Instability (defined by symptoms such as giving way, perceived instability and at least one LAS within the last 6 months) * Previous ATR * Other lower limb injury and/or surgery in the last year (e.g. fractures, ligament reconstructions or other conditions resulting in ≥ 6 months of sports inactivity) * Impaired motor function of the lower limb due to neurovascular or neurological diseases * Vestibular or visual disturbances * Or any other pathoanatomic abnormality that would affect motor performance (e.g. foot arthrodesis, toe amputation/missing toes or other conditions such as joint deformities, severe chronic pain).
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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Other studies related to the condition(s) this trial covers.
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