NCT07521215

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
4mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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 Progress35%
Apr 2026Nov 2026

Study Start

First participant enrolled

April 1, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

April 3, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 9, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Expected
Last Updated

April 9, 2026

Status Verified

April 1, 2026

Enrollment Period

2 months

First QC Date

April 3, 2026

Last Update Submit

April 3, 2026

Conditions

Keywords

injury preventionindividualized exerciseY-Balance TestHop TestLimb Symmetry IndexGIRDCKCUESTuniversity athletesbasketballvolleyballfunctional screeningneuromuscular training

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

EXPERIMENTAL

Athletes 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.

Behavioral: Test-Specific Individualized Exercise Program

Observation (No Intervention)

NO INTERVENTION

Athletes 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.

Individualized Exercise Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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)

Location

MeSH Terms

Conditions

Athletic Injuries

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Officials

  • Ali Omer Acar

    Acibadem Mehmet Ali Aydinlar University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation

    PRINCIPAL INVESTIGATOR

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
Model Details: Non-randomized parallel assignment. Athletes scoring below literature-defined cut-off values on any clinical/functional test are assigned to the Intervention Group and receive test-specific individualized exercise prescriptions. Athletes meeting all cut-off thresholds are assigned to the Observation Group and receive no intervention. Group assignment is determined by baseline test performance, not by randomization.
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

Locations