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Recruiting NCT06774547

NCT06774547 Early Implementation of Plyometric Exercises in the Rehabilitation of Individuals Suffering From Lower-Extremity Tendinopathies

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Clinical Trial Summary
NCT ID NCT06774547
Status Recruiting
Phase
Sponsor Aalborg University
Condition Achilles Tendinopathy
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2025-09-18
Primary Completion 2027-10

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 50 Years
Study Type INTERVENTIONAL
Interventions
Heavy-slow resistance trainingPlyometric exercise

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2025-09-18 with a primary completion date of 2027-10.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This clinical trial aims to compare the effectiveness of an early plyometric exercise approach with traditional heavy, slow resistance training in treating tendinopathies of the Achilles tendon, patellar tendon, and plantar fascia. These conditions, commonly seen in general and rheumatology practices, cause pain, reduced function, and stiffness, often leading to prolonged recovery and incomplete return to full physical activity. The study hypothesizes that introducing plyometric exercises early in rehabilitation will improve jump function after 12 weeks and reduce re-injury rates within 52 weeks compared to traditional methods. The study is a randomized clinical trial including 120 participants aged 18-50 with tendinopathy in one of the targeted areas. Participants must regularly engage in running or jumping sports, have symptoms for at least three months, and meet other inclusion criteria. Exclusion criteria include recent surgery or specific medical conditions. Both groups will perform exercises three times weekly for 12 weeks, tailored to their tendinopathy. The intervention group will add progressive plyometric exercises to the standard strength training performed by the control group. Plyometric training will consist of three levels, with patients self-assessing readiness to progress. The primary outcome is the change in the plyometric quotient, a measure of functional ability, based on a jump test using a force platform at 0 and 12 weeks. Secondary outcomes include dynamic strength, jump height, patient-reported symptoms (via questionnaires), return to sport, training compliance, adverse events, pain thresholds, re-injury rates, and psychological readiness for sports. Assessments will occur at baseline, 12 weeks, and 52 weeks.

Eligibility Criteria

Inclusion Criteria: 1. participants are required to have performed either recreational running or participated in sports that include running or jumping activities (e.g., football, basketball, handball, volleyball) at least once per week for at least three months immediately prior to pain onset 2. have had symptoms for at least three months 3. have pain/soreness with palpation of the tendon/fascia 4. mean pain during the past week of at least 2 on a 0 to 10 Numerical Rating Scale 5. pain during a pain provocation test (patellar tendinopathy: five single-legged decline squats, Achilles tendinopathy and plantar fasciopathy: ten single-legged heel raises) Exclusion Criteria: 1. previous lower-extremity surgery 2. other lower-extremity musculoskeletal conditions that have required treatment by a healthcare professional during the past three months 3. pregnancy 4. diabetes 5. history of inflammatory systemic diseases (e.g., rheumatoid arthritis or spondylarthritis) 6. having received an injection with corticosteroid within the past six months.

Contact & Investigator

Central Contact

Henrik Riel, PhD

✉ heri@ucn.dk

📞 0045 72691014

Frequently Asked Questions

Who can join the NCT06774547 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 50 Years, studying Achilles Tendinopathy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06774547 currently recruiting?

Yes, NCT06774547 is actively recruiting participants. Contact the research team at heri@ucn.dk for enrollment information.

Where is the NCT06774547 trial being conducted?

This trial is being conducted at Aalborg, Denmark.

Who is sponsoring the NCT06774547 clinical trial?

NCT06774547 is sponsored by Aalborg University. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology