Individualized Rehabilitation for Osgood-Schlatter or Sever Pain in Youth Athletes

NCT ID
NCT07521280
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Medical University of Gdansk
Conditions
Apophyseal Pain, Osgood-Schlatter Disease, Sever's Disease, Sinding-Larson and Johansson Syndrome (SLJ)

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: Feasibility, Clinical Response, and Exploratory Predictors of an Individualized Load-Based Rehabilitation Pathway in Youth Athletes With Osgood-Schlatter Disease or Sever Disease: A Prospective Single-Arm Interventional Study

Enrollment: 45 participants (Estimated).

What is being studied

  • Behavioral: Individualized Load-Based Rehabilitation Pathway

Who may be eligible

Ages
10 Years to 17 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Aged 10 to 17 years * Participates in organized sport and has at least 12 months of sport participation or training history * Has current lower-extremity apophyseal pain consistent with Osgood-Schlatter-related knee pain, Sever-related heel pain, and/or Sinding-Larsen-Johansson-related pain at the inferior pole of the patella, or has previous symptoms of these conditions with a residual or low-irritability presentation relevant to rehabilitation * Meets criteria for at least one pre-specified rehabilitation entry pathway: post-trial rehabilitation entry after completion of the separate photobiomodulation trial, or direct-entry rehabilitation with active apophyseal symptoms, or direct-entry rehabilitation with previous Osgood-Schlatter-related or Sever-related symptoms and a low-irritability or residual presentation For participants entering with active symptoms: * pain is located at the tibial tubercle region, the inferior pole of the patella, and/or the calcaneal apophyseal/heel region * pain is aggravated by activity, loading, or sport participation * pain is reproducible on clinical examination or the clinical history is consistent with the target condition Participant and parent/caregiver are willing to take part in the rehabilitation program, including in-person visits, home exercises, symptom/activity monitoring, and follow-up assessments. A parent or legal guardian provides written informed consent, and the participant provides assent when applicable. Exclusion Criteria: * Current pain episode started after an acute traumatic injury that better explains the symptoms * Clinical presentation suggests a condition other than the target rehabilitation condition, including a major alternative knee or heel diagnosis requiring different management * Lower-limb surgery that would substantially affect rehabilitation planning, safety, or interpretation of outcomes * Known serious musculoskeletal, neurological, rheumatological, inflammatory, autoimmune, metabolic, or other systemic disease that may affect safe participation or interpretation of outcomes * Any medical or developmental condition that would prevent safe participation in exercise-based rehabilitation * Current symptoms requiring urgent medical assessment or management outside the rehabilitation pathway * Inability to understand study instructions or complete study procedures with parent/caregiver support * Parent/caregiver or participant does not agree to participate or withdraws consent/assent

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: Poland

  • Debinki 7, Poland: 1

Sample of listed locations

  • Department of Immunobiology and Environment Microbiology — Gdansk, Debinki 7, 80-210, Poland — Recruiting

Study details

Start date
April 20, 2026
Primary completion date
June 30, 2027
Completion date
April 5, 2029
First posted
April 9, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07521280
Registry last updated
October 9, 2026
QualifiedStudies registry data refreshed
October 12, 2026
QualifiedStudies record fetched
October 12, 2026

View NCT07521280 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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