Evaluation of Injury Risk Factors and Effects of Individualized Exercise Program in Basketball and Volleyball Athletes
IRISPORT
2 other identifiers
interventional
100
1 country
1
Brief Summary
This study aims to identify injury risk factors using a clinical/functional test battery in university basketball and volleyball athletes, to develop individualized exercise prescriptions for athletes scoring below established cut-off values on each test, and to evaluate the effects of an 8-week intervention program on test parameters. As a secondary aim, all participants will be monitored prospectively over a 6-month season to assess the incidence of injuries and health problems, and to evaluate the contribution of the individualized program to injury-related health outcomes. The study consists of four phases: (1) baseline cross-sectional assessment (T0), (2) 8-week individualized exercise intervention for athletes below cut-off thresholds, (3) post-intervention reassessment (T1), and (4) 6-month prospective injury surveillance (T2).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
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
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 3, 2026
CompletedFirst Posted
Study publicly available on registry
April 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2026
ExpectedApril 9, 2026
April 1, 2026
2 months
April 3, 2026
April 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Change in Y-Balance Test Lower Quarter (YBT-LQ) Composite Score
Composite score calculated as \[(Anterior + Posteromedial + Posterolateral) / (3 x Leg Length)\] x 100. Assessed bilaterally. Cut-off: composite score less than 94% or right-left asymmetry greater than 4 cm.
Baseline (T0) and 8 weeks (T1)
Change in Hop-for-Distance Test Limb Symmetry Index (LSI)
LSI calculated as (Weaker Side / Stronger Side) x 100. Three trials per limb, best distance recorded. Cut-off: LSI less than 90%.
Baseline (T0) and 8 weeks (T1)
Change in Active Straight Leg Raise (ASLR) Hip Flexion Angle
Hip flexion range of motion measured by goniometry in supine position with knee extended. Two measurements per limb, average recorded. Cut-off: hip flexion less than 70 degrees.
Baseline (T0) and 8 weeks (T1)
Change in Closed Kinetic Chain Upper Extremity Stability Test (CKCUEST) Score
Number of hand touches in 15 seconds from push-up position with hands 91 cm apart. Three trials, best score recorded. Cut-off: males less than 21 touches, females less than 23 touches.
Baseline (T0) and 8 weeks (T1)
Change in Glenohumeral Internal Rotation Deficit (GIRD)
Internal and external rotation measured by goniometry in supine (shoulder 90 degrees abduction, elbow 90 degrees flexion), scapula stabilized. GIRD = non-dominant IR minus dominant IR. Cut-off: IR deficit greater than 20 degrees or total rotation difference greater than 5 degrees.
Baseline (T0) and 8 weeks (T1)
Secondary Outcomes (3)
Incidence of Musculoskeletal Injuries and Health Problems
6 months (T0 through T2)
Pittsburgh Sleep Quality Index (PSQI) Global Score
Baseline (T0)
Borg Rating of Perceived Exertion (RPE)
Baseline (T0)
Study Arms (2)
Individualized Exercise Intervention
EXPERIMENTALAthletes scoring below established literature cut-off values on one or more clinical/functional tests at baseline (T0). Each athlete receives a test-specific individualized exercise prescription targeting their identified deficits. The program is administered 3 days/week for 8 weeks (20-30 min/session), with supervised sessions in weeks 1-2 and partially independent sessions in weeks 3-8.
Observation (No Intervention)
NO INTERVENTIONAthletes meeting all literature-defined cut-off thresholds on every clinical/functional test at baseline (T0). These athletes continue their routine training without additional exercise intervention. They undergo the same T0 and T1 assessments and 6-month injury surveillance as the intervention group.
Interventions
An 8-week individualized exercise program prescribed based on each athlete's baseline test deficits. Components include: 1. Dynamic balance/proprioception exercises (for YBT-LQ deficit): single-leg balance progressions, 3-direction reach drills, BOSU balance exercises. 2. Plyometric control and symmetry exercises (for Hop Test LSI deficit): single-leg hop-and-stick, lateral hops, eccentric step-up/step-down. 3. Hamstring/posterior chain flexibility exercises (for ASLR deficit): static hamstring stretching with strap, PNF contract-relax, seated hamstring stretch. 4. Scapular stability and upper extremity endurance exercises (for CKCUEST deficit): plank shoulder taps, bear crawl, side plank progressions. 5. Posterior shoulder capsule and rotator cuff exercises (for GIRD deficit): cross-body stretch, sleeper stretch, external rotation with resistance band. Dosage: 3 sessions/week, 20-30 minutes/session. Progressive overload applied. Weekly compliance monitored.
Eligibility Criteria
You may qualify if:
- Active member of Acibadem University basketball or volleyball team
- Regular training within the past 6 months
- Age 18 years or older
- Willing to participate and provide written informed consent
- Physical and cognitive capacity to complete test protocols
You may not qualify if:
- Surgical intervention within the past 6 months
- Acute musculoskeletal injury within the past 2 weeks (acute sprain/strain/contusion etc.) that would preclude testing
- History of vestibular disorder, neurological disease, or systemic condition that may affect balance testing
- Uncontrolled cardiovascular disease/hypertension or other medical condition contraindicating exercise
- Pregnancy or within the first 6 months postpartum (female athletes)
- Refusal to provide informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Acibadem Mehmet Ali Aydinlar University, Department of Physiotherapy and Rehabilitation
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ali Omer Acar
Acibadem Mehmet Ali Aydinlar University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Masking Details
- Open label. No masking is employed. Group allocation is based on objective test results against pre-defined cut-off values, making blinding not feasible.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer, Department of Physiotherapy and Rehabilitation
Study Record Dates
First Submitted
April 3, 2026
First Posted
April 9, 2026
Study Start
April 1, 2026
Primary Completion
June 1, 2026
Study Completion (Estimated)
November 1, 2026
Last Updated
April 9, 2026
Record last verified: 2026-04