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NOT YET RECRUITING
NCT07466407
NA

Effects of HMB and Rehabilitation Program in Athletes With Patellar Tendinopathy

Sponsor: Universidad Complutense de Madrid

View on ClinicalTrials.gov

Summary

This randomized, double-blind, placebo-controlled clinical trial evaluates the effects of oral beta-hydroxy-beta-methylbutyrate (HMB) supplementation combined with an eccentric exercise and extracorporeal shockwave rehabilitation program on pain, tendon morphology, and neuromuscular performance in athletes with patellar tendinopathy. Thirty athletes with a confirmed diagnosis of patellar tendinopathy are randomized to receive either HMB supplementation (3 g/day) or placebo during an 8-week rehabilitation program. Participants are evaluated at baseline, week 4, and week 8. The primary outcome is pain and functional limitation assessed using the Victorian Institute of Sport Assessment-Patella (VISA-P) questionnaire. Secondary outcomes include patellar tendon thickness measured by ultrasound imaging, countermovement jump (CMJ) performance, and neuromuscular performance variables derived from an incremental squat test using a linear position transducer. The aim of the study is to determine whether HMB supplementation enhances clinical recovery and neuromuscular performance when combined with a standardized rehabilitation program compared with placebo.

Official title: Effects of Beta-Hydroxy-Beta-Methylbutyrate (HMB) Supplementation in Athletes With Patellar Tendinopathy

Key Details

Gender

All

Age Range

18 Years - 49 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-03-01

Completion Date

2026-07-01

Last Updated

2026-03-12

Healthy Volunteers

No

Interventions

OTHER

Eccentric exercise and extracorporeal shock wave therapy

Participants undergo a standardized rehabilitation program consisting of eccentric exercise and extracorporeal shock wave therapy.

DIETARY_SUPPLEMENT

Beta-hydroxy-beta-methylbutyrate (HMB)

Participants ingest 3 g/day of beta-hydroxy-beta-methylbutyrate (HMB) in capsule form, administered 60 minutes before each eccentric training session during the 8-week intervention period.

Locations (1)

Clínica Fisio-Agil

Córdoba, Córdoba, Spain