New exercise may ease Jumper's knee in weightlifters
NCT ID NCT07361848
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a long-hold isometric exercise can reduce pain and improve function in competitive weightlifters with patellar tendinopathy (jumper's knee). About 24 athletes will either do the supervised exercise or follow routine training. Researchers will measure pain, tendon health via ultrasound, and performance to see if this approach is safe and effective.
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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 24 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2027
An estimate. Start dates often move.
- Expected to finish
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Apr 2028
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 45 years
- 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: 1. Competitive weightlifting athletes (Olympic weightlifting or CrossFit) training ≥3 times per week. 2. Age 18-45 years. 3. Symptom duration of at least 6 weeks. 4. Presence of vascularized patellar tendinopathy, defined as Doppler-detectable intratendinous neovascularization using standardized settings. 5. VISA-P score \< 80 at baseline. 6. Ability to perform loaded lower-limb exercises safely. 7. Willingness to refrain from other structured isometric interventions focused on the patellar tendon during the study period. 8. Ability to provide informed consent. 9. Sex/Gender requirement: both men and women eligible; the study includes sex-stratified analysis to examine potential sex-based differences in tendon response. Exclusion Criteria: 1. Previous knee surgery within the past 12 months. 2. Partial or complete patellar tendon rupture (confirmed clinically or by ultrasound). 3. Coexisting knee conditions (e.g., meniscal tear, ACL/PCL injury, patellofemoral joint instability) that significantly affect load tolerance. 4. Systemic diseases affecting tendon health (e.g., diabetes, rheumatoid arthritis, connective tissue disorders). 5. Corticosteroid injection in the patellar tendon within the last 6 months. 6. Participation in other clinical trials involving exercise or tendon-loading interventions. 7. Neuromuscular or medical conditions limiting safe performance of isometric or plyometric exercise. 8. Pregnancy. 9. Inability to commit to follow-up assessments at 8, 12, and 24 weeks.
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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
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Contacts and locations
Locations
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Universidad Complutense de Madrid, Faculty of Nursing, Physiotherapy and Podiatry, Department of Physiotherapy
Madrid, Madrid, 28040, Spain
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