Eccentric decline squat protocol offers superior results at 12 months compared with traditional eccentric protocol for patellar tendinopathy in volleyball players.
M A Young, J L Cook, C R Purdam...
https://pubmed.ncbi.nlm.nih.gov/15665207/Actively Recruiting
Led by University of Valencia · Updated on 2026-06-25
42
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the effectiveness of transcranial direct current stimulation tDCS combined with a therapeutic eccentric exercise program in people with patellar tendinopathy, a painful condition affecting the front of the knee. This randomized clinical trial compares two groups one receiving real tDCS plus exercise and the other receiving sham tDCS plus exercise. The study aims to understand how these treatments affect pain, functionality, muscle strength, proprioception, and quality of life. Participants will engage in an 8-week program involving supervised eccentric exercise sessions three times per week with a physiotherapist, plus additional unsupervised exercises at home on other weekdays. The experimental group will receive real tDCS applied at 1.5 mA for 20 minutes to the primary motor cortex during the first four weeks of exercise sessions. The control group will receive sham tDCS where the current is stopped after 30 seconds. Assessments are planned at baseline, week 4, week 8, and week 12. During the study, participants will be evaluated on knee functionality, pain intensity, quality of life, muscle strength and activity, muscle flexibility, tone, proprioception, and their overall perception of change. These assessments will involve various tests lasting from 1 to 10 minutes. The trial is designed to monitor progress and treatment effects over 12 weeks, including four scheduled assessment points.
CONDITIONS
Transcranial Direct Current Stimulation on Functionality and Pain in Individuals With Patellar Tendinopathy
M
Marta Inglés, Dr
E
Elena Muñoz-Gómez, Dr
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University of Valencia
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive supervised eccentric exercise sessions three times per week for 8 weeks, combined with either real or sham tDCS during the first 4 weeks. They also perform unsupervised exercises at home on other weekdays.
3 supervised sessions per week plus home exercises
Duration - 12 weeks from baseline
Participants undergo assessments at baseline, week 4, week 8, and week 12 to measure pain, knee function, muscle strength, proprioception, and quality of life.
4 assessment visits
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Lead Sponsor