Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
ID06774547

The Efficacy of Early Implementation of Plyometric Exercises in the Rehabilitation of Individuals Suffering From Lower-Extremity Tendinopathies: A Randomised Clinical Trial

Led by Aalborg University · Updated on 2026-03-04

120

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

A

Aalborg University

Lead Sponsor

D

Department of Physiotherapy, University College of Northern Denmark

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether an early plyometric exercise approach improves recovery compared to traditional heavy, slow resistance training in people with tendinopathies of the Achilles tendon, patellar tendon, or plantar fascia. These common conditions cause pain, reduced function, and stiffness, often leading to long recovery times and incomplete return to sports. The study aims to see if early plyometric exercises can improve jump function after 12 weeks and reduce re-injury rates after 52 weeks. The trial includes 120 participants aged 18 to 50 who regularly engage in running or jumping sports and have symptoms lasting at least three months. Participants are randomly assigned to two groups: one performs heavy slow resistance training alone, while the other combines this training with a progressive plyometric exercise program. Both groups exercise three times weekly for 12 weeks, with plyometric training progressing through three levels based on self-assessed readiness. Participants will be assessed at the start, after 12 weeks, and at 52 weeks. Tests include measuring jump function using a force platform, dynamic strength, jump height, and pain thresholds. Questionnaires will capture symptoms, exercise compliance, return to sport, adverse events, re-injury rates, and psychological readiness. The main measure is the change in plyometric quotient over 12 weeks, showing functional ability improvements.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 50 years
  • Regularly perform running or jumping sports at least once per week for the three months before pain started
  • Have symptoms lasting at least three months
  • Have pain or soreness when pressing the affected tendon or fascia
  • Have average pain of at least 2 on a 0 to 10 scale in the past week
  • Experience pain during specific tendon tests (decline squats or heel raises)
Not Eligible

You will not qualify if you...

  • Previous lower-extremity surgery
  • Other recent lower-extremity musculoskeletal conditions treated in the past three months
  • Pregnancy
  • Diabetes
  • History of inflammatory systemic diseases like rheumatoid arthritis or spondylarthritis
  • Received corticosteroid injection in the affected area within the past six months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants undergo a 12-week intervention consisting of heavy-slow resistance training, with some participants also performing a plyometric exercise program. Exercises are performed unsupervised three times per week with progression based on tolerable pain and readiness.

Weekly visits for progress assessments

Follow-up

Duration - Up to 40 weeks after treatment

Participants are monitored for outcomes such as plyometric quotient, strength, pain, and return to sport for up to 52 weeks after the intervention.

Visits at 12-week and 52-week follow-ups

Trial Site Locations

Total: 1 location

1

University College of Northern Denmark

Aalborg, Denmark, 9220

Actively Recruiting

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Research Team

H

Henrik Riel, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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