Why do patients quit their tendon exercises? new study aims to find out
NCT ID NCT07555184
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
Achilles tendinopathy causes pain and stiffness in the ankle tendon, making daily activities hard. The main treatment is a program of specific exercises, but many people struggle to keep them up. This study will interview up to 30 adults who have had NHS physiotherapy for this condition to understand what helps or hinders them from sticking with the exercises. The goal is to use these insights to design better support for future patients.
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 study could point toward better ways to support people with Achilles tendinopathy to complete their exercise programs, making treatment more effective.
- What could go wrong
- This is a small, early-stage interview study with only 30 participants, so findings may not apply to everyone. It does not test a treatment itself.
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.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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May 2027
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.
Who is studied
The study population will comprise adults aged 18 years and over with lived experience of Achilles tendinopathy who have previously received, and attempted to follow, an NHS-prescribed progressive tendon-loading exercise programme within the past 24 months. Participants will be recruited from NHS musculoskeletal service records, community engagement routes, and individuals who have previously expressed interest in Achilles tendon research. The study will use purposive sampling to achieve diversity in age, gender, ethnicity, socioeconomic background, and clinical characteristics, with particular emphasis on including underserved groups such as people living with multimorbidity, socioeconomic disadvantage, cultural or language barriers, or other factors that may affect engagement with rehabilitation.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 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.
Inclusion Criteria: * • Adults aged 18 years or over with lived experience of Achilles tendinopathy (AT). * Gender representation: A purposive sample including men and women, with inclusion of non-binary participants where self-identified, aiming for broad gender representation rather than fixed quotas. * Ethnic and cultural diversity: Purposive sampling will seek representation from diverse ethnic and cultural backgrounds, informed by local population demographics and service user profiles. * Socioeconomic diversity: Participants will be recruited across high, mid, and low socioeconomic deprivation groups, defined using postcode-derived Index of Multiple Deprivation (IMD) tertiles (lower, middle, upper thirds of national IMD distribution). Recruitment will aim for representation across all three IMD categories rather than predefined percentages. Exclusion Criteria: * • Under 18 years of age * Inability to confirm previous AT through either ELHT electronic medical records or through discussion with CI * Individuals whose Achilles symptoms are due to a different primary pathology (e.g., Rheumatological, Achilles Rupture) * Unable to provide informed consent * Unable or unwilling to be audio-recorded.
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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East Lancashire Hospitals Trust
Blackburn, BB2 3HH, United Kingdom
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