Effects of HMB and Rehabilitation Program in Athletes With Patellar Tendinopathy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-49
SponsorUniversidad Complutense de Madrid

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18 and 49 years

Clinical diagnosis of patellar tendinopathy confirmed by a physician and physiotherapist

Competitive athlete in sports involving repetitive knee loading (e.g., basketball, volleyball, handball, athletics)

Minimum training frequency of three sessions per week

Disqualifiers

Any musculoskeletal injury other than patellar tendinopathy affecting performance

Systemic disease affecting musculoskeletal function

Inability to comply with the rehabilitation or supplementation protocol

Trial design

Design model

Parallel

Treatments tested in this trial

  • Eccentric exercise and extracorporeal shock wave therapy

    Other intervention

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

  • Beta-hydroxy-beta-methylbutyrate (HMB)

    Dietary supplement

    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.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: HMB Supplement + Rehabilitation ProgramExperimental treatment 2 interventions
Group B: Placebo + Rehabilitation ProgramPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

VISA-P Score

Change in pain and functional limitation assessed using the Victorian Institute of Sport Assessment-Patella (VISA-P) questionnaire. Scores range from 0 to 100, with higher scores indicating better function and lower pain levels.

Time frame
Baseline (PRE), Week 4 (INT), and Week 8 (POST)

Secondary outcomes

1

Patellar tendon thickness

Change in patellar tendon thickness (mm) measured by ultrasound imaging using a standardized longitudinal scanning protocol

Time frame
Baseline (PRE), Week 4 (INT), and Week 8 (POST)
2

Countermovement Jump (CMJ)

hange in countermovement jump (CMJ) height measured in centimeters using a contact platform. Participants will perform three maximal attempts, and the highest value will be recorded

Time frame
Baseline (PRE), Week 4 (INT), and Week 8 (POST)
3

Peak Power (PP) during squat test

Change in peak power (PP) measured in watts during an incremental squat test using a linear position transducer.

Time frame
Baseline (PRE), Week 4 (INT), and Week 8 (POST)
4

Peak Power Relative to Body Mass (PPkg)

Change in peak power relative to body mass (PPkg) measured in watts per kilogram during an incremental squat test using a linear position transducer.

Time frame
Baseline (PRE), Week 4 (INT), and Week 8 (POST)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Universidad Complutense de Madrid

Lead sponsor

Universidad de Córdoba

Collaborator

University of Seville

Collaborator

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