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Combined Physical Therapy and Hold-Relax Technique for Adolescent Osgood-Schlatter Knee Pain

Exploratory Effects of a Combined Hold-Relax Technique and Progressive Rehabilitation Program on Knee Pain in Adolescent Athletes With Osgood-Schlatter Disease: A Pilot Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07590128
Enrollment
6
Registered
2026-05-15
Start date
2026-01-02
Completion date
2026-04-15
Last updated
2026-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osgood-Schlatter Disease

Brief summary

This pilot study evaluates the preliminary effectiveness of a combined rehabilitation program incorporating hold-relax (H-R) stretching techniques and progressive therapeutic exercises on knee pain and range of motion (ROM) in adolescent athletes diagnosed with Osgood-Schlatter disease. Utilizing a retrospective, single-group pre-post design on a cohort of six athletic participants, this study aims to generate preliminary clinical evidence and assess feasibility to inform future larger-scale randomized controlled trials. Participants underwent a structured, multi-week rehabilitation protocol, with primary clinical outcomes assessed before and after the intervention period using validated measures of pain intensity and knee joint mobility.

Interventions

BEHAVIORALHold-Relax Proprioceptive Neuromuscular Facilitation (PNF)

A target-specific, manual stretching technique administered by a physical therapist to address muscular tightness in the lower extremity. The protocol focuses on the bilateral quadriceps and hamstring muscle groups to reduce the cumulative tensile traction forces exerted on the tibial tuberosity. For each target muscle group, the procedure is performed as follows: Passive Stretch: The physical therapist moves the joint to the limit of comfortable range of motion (ROM) where mild muscle tightness is felt. Isometric Contraction: The participant performs an active, sub-maximal isometric contraction (approximately 50% of maximum voluntary contraction) against the therapist's manual resistance for 6 to 10 seconds, ensuring no actual joint movement occurs. Relaxation and Deeper Passive Stretch: The participant is instructed to relax completely, and the therapist immediately moves the limb passively into a newly gained, deeper range of motion, holding the stati

A structured, step-by-step active exercise program designed to build lower-limb load tolerance, correct biomechanical compensations, and stabilize the knee joint complex. The rehabilitation progresses systematically through targeted phases based on individual pain levels and movement quality:Phase 1 (Pain Mitigation and Muscle Activation): Focuses on isometric quadriceps setting, straight leg raises (SLR), gluteal bridging, and ankle/hip mobility exercises to avoid direct loading of the patellar tendon while minimizing disuse atrophy.Phase 2 (Strength and Load Tolerance): Introduces closed-kinetic chain exercises with controlled ranges of motion, including shallow wall sits, leg presses, bilateral squats, and progressive calf raises.Phase 3 (Eccentric and Functional Progression): Focuses on eccentric quadriceps strengthening (e.g., controlled step-downs) and sport-specific functional retraining to prepare the adolescent athlete's patellar tendon and tibial tubercle to absorb high groun

Sponsors

Benha University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
14 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of Osgood-Schlatter disease * Presence of anterior knee pain localized at the tibial tuberosity * Regular participation in sports involving running and jumping * No participation in structured rehabilitation programs within the previous 3 months

Exclusion criteria

* History of knee surgery or major trauma * Presence of other knee pathologies (e.g., ligament or meniscal injuries) * Neurological or systemic disorders affecting movement

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Knee Pain Intensity on the Visual Analog Scale (VAS)Baseline (Day 1, pre-intervention) and post-intervention (Week 10, immediately following completion of the last rehabilitation session).Knee pain during athletic activity is assessed using a 10-centimeter Visual Analog Scale (VAS). The scale is a horizontal line where 0 centimeters indicates "no pain" and 10 centimeters indicates "the worst possible pain." The outcome is calculated as the change in the pain score (post-intervention score minus baseline score). A negative change indicates an improvement (reduction) in knee pain.

Secondary

MeasureTime frameDescription
Change from Baseline in Active Knee Flexion Range of MotionBaseline (Day 1, pre-intervention) and post-intervention (Week 10, immediately following completion of the last rehabilitation session).Active knee joint flexion range of motion measured in degrees of joint angle using a standard universal goniometer. The participant lies in a supine position and actively bends the knee as far as possible. The outcome is calculated as the change in degrees from baseline to post-intervention. An increase in degrees indicates an improved range of motion.

Countries

Algeria

Contacts

PRINCIPAL_INVESTIGATORMahmoud El sayed, Bachelor of Physical Therapy

Benha University

PRINCIPAL_INVESTIGATORAhmed Said, Bachelor of Physical Therapy

Benha University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 16, 2026