Measuring recovery after Achilles tendon rupture
The Impact of Achilles Tendon Rupture on the Structure and Function of the Achilles Tendon and Plantarflexors: a Longitudinal Cohort Study
University of Leicester · NCT05683080
This study looks at how people recover after an Achilles tendon rupture by checking their tendon, strength, and daily activities over the course of a year.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 60 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | University of Leicester (other) |
| Locations | 1 site (Leicester) |
| Trial ID | NCT05683080 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the recovery process following an Achilles tendon rupture. Participants will undergo a series of evaluations, including ultrasound scans of the tendon, calf strength tests, and various questionnaires to gauge their everyday functioning. Measurements will be taken at multiple time points: upon arrival at the clinic, and then at 8 weeks, 10 weeks, 4 months, 6 months, and 1 year post-injury. The study seeks to provide a comprehensive understanding of recovery dynamics in affected individuals.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 16 and older who have experienced an Achilles tendon rupture.
Not a fit: Patients who are unable to provide informed consent due to cognitive impairment or language barriers may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance rehabilitation strategies for patients recovering from Achilles tendon ruptures.
How similar studies have performed: While there have been studies on Achilles tendon injuries, this specific observational approach focusing on comprehensive recovery metrics is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Able to provide informed consent * 16 years of age or above Exclusion Criteria: * Inability to provide informed consent due to cognitive impairment * Inability to provide informed consent as unable to understand sufficient English
Where this trial is running
Leicester
- University Hosptial of Leicester NHS Trust — Leicester, United Kingdom (RECRUITING)
Study contacts
- Study coordinator: Samuel Briggs-Price
- Email: sbp18@leicester.ac.uk
- Phone: 01162525141
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Achilles Tendon Rupture