Screening of Adductor Related Symptoms in Adolescent Taekwondo Athletes
Screening of Adductor-Related Symptoms and Comparison of Hip Muscle Strength, Range of Motion, and Functional Level Between Symptomatic and Asymptomatic Adolescent Taekwondo Athletes
1 other identifier
observational
80
1 country
1
Brief Summary
The goal of this observational study is to learn about the frequency and characteristics of adductor-related groin symptoms in adolescent Taekwondo athletes aged 12-17 years. The main questions it aims to answer are: How common are adductor-related groin symptoms in adolescent Taekwondo athletes? Do athletes with these symptoms show differences in hip strength, joint range of motion, or functional level compared to athletes without symptoms? Participants will complete a brief screening about their groin pain and training habits, followed by: Clinical tests of the hip and groin region (resisted adduction, palpation, FABER, and FADIR tests) Strength testing of hip abductor and adductor muscles using a hand-held dynamometer Range of motion measurements of the hip using a goniometer A self-reported questionnaire (Copenhagen Hip and Groin Outcome Score - HAGOS) to assess daily activity and sports function Data from this study will help identify early signs of adductor-related groin problems and guide preventive and rehabilitation strategies for young Taekwondo athletes
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 25, 2026
CompletedFirst Submitted
Initial submission to the registry
February 2, 2026
CompletedFirst Posted
Study publicly available on registry
February 13, 2026
CompletedFebruary 13, 2026
February 1, 2026
3 months
February 2, 2026
February 7, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Prevalence of Adductor-Related Groin Symptoms
The presence of adductor-related groin symptoms will be assessed using standardized clinical tests (resisted adduction test and adductor palpation test) based on the Doha classification framework. Unit of Measure: Percentage of athletes with positive test results (%) Purpose: To determine how common adductor-related groin symptoms are among adolescent Taekwondo athletes. Type: Categorical (Yes/No)
at baseline
Pain Intensity
Pain intensity during resisted adduction will be evaluated using a Numeric Pain Rating Scale (NPRS; 0-10). Unit of Measure: Points (0-10 scale). Higher points indicates severe pain. Purpose: To quantify the severity of pain in athletes with adductor-related symptoms.
at baseline
Secondary Outcomes (6)
Isometric Hip Adductor Strength
at baseline
Isometric Hip Abductor Strength
at baseline
Eccentric Hip Adductor Strength
at baseline
Eccentric Hip Abductor Strength
at baseline
Hip Range of Motion (Abduction and Internal Rotation)
at baseline
- +1 more secondary outcomes
Study Arms (2)
Symptomatic Group (Adductor-Related Groin Pain Group)
This group will include adolescent Taekwondo athletes aged 12-17 years who report groin pain or discomfort during training and test positive for adductor-related symptoms based on the Doha classification framework. Diagnosis of adductor-related groin pain will be confirmed through: Resisted adduction test (pain provocation) Palpation of adductor muscles and tendons Participants in this group will undergo hip strength, range of motion, and functional assessments.
Asymptomatic Control Group (Healthy Control Group)
This group will include age-, sex-, and activity-matched adolescent Taekwondo athletes who do not report groin pain or any lower extremity injury and test negative on the clinical provocation tests (resisted adduction, palpation, FABER, FADIR). They will undergo the same measurements as the symptomatic group for comparison.
Eligibility Criteria
The study population consisted of adolescent Taekwondo athletes aged 12 to 17 years who are actively training at the Göztepe Sports Club, İzmir, Türkiye. All participants held a black belt (professional level) and have at least three years of competitive Taekwondo experience with regular training sessions at least five times per week. Two groups formed: Symptomatic Group: Athletes who report groin pain or discomfort during training and show positive results on clinical tests for adductor-related groin symptoms (resisted adduction and palpation tests). Asymptomatic Control Group: Age-, sex-, and activity-matched athletes without groin pain or any lower extremity symptoms, who test negative on all clinical examinations. All participants are screened by a physiotherapist for eligibility prior to data collection.
You may qualify if:
- Aged between 12 and 17 years.
- Registered as an active Taekwondo athlete at a Sports Club.
- Holds a black belt level (professional) in Taekwondo.
- Has at least 3 years of professional Taekwondo training experience.
- Participates in training sessions at least 5 days per week.
- Able to participate in regular training and competition without restriction.
- Voluntarily agrees to participate and provides informed consent (and parental consent for minors).
You may not qualify if:
- Presence of any orthopedic, neurological, or systemic condition that may affect lower limb function or limit participation in training.
- History of lower extremity surgery (hip, knee, ankle, or foot).
- Current or recent (within the last 6 months) acute lower extremity injury other than groin-related symptoms.
- Refusal or inability to complete the required clinical tests or questionnaires.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Izmir Democracy University
Izmir, İzmir, 35290, Turkey (Türkiye)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 7 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assist. Prof.
Study Record Dates
First Submitted
February 2, 2026
First Posted
February 13, 2026
Study Start
October 15, 2025
Primary Completion
January 15, 2026
Study Completion
January 25, 2026
Last Updated
February 13, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share