Shoulder Injury Prevention in Adolescent Handball Players Based on Scandinavian Protocols

Not Applicable

Active, not recruiting

• Conditions: Injury Prevention; Shoulder Injuries

• Registration Number: NCT07146243
• Lead Sponsor: Semmelweis University

Brief Summary

This cluster-randomised controlled trial will evaluate the effects of two internationally recognised shoulder injury prevention programmes - the Swedish Shoulder Control programme and the Norwegian Oslo Sports Trauma Research Center Shoulder Injury Prevention programme - on shoulder function, scapular control, and injury incidence in Hungarian adolescent handball players (U16-U20). Six elite-level teams (3 male, 3 female) from a single handball academy will be randomised by cluster into two intervention arms for an 18-week intervention period. Primary outcomes are changes in objective shoulder function tests; secondary outcomes include self-reported function and weekly injury monitoring.

Detailed Description

This study is a two-armed cluster-randomised controlled trial designed to assess the effects of two established, evidence-based shoulder injury prevention programmes in Hungarian adolescent elite handball players. Both programmes have previously demonstrated effectiveness in reducing the incidence of shoulder injuries in overhead athletes; however, it remains unclear how they compare in their ability to improve specific objective outcomes such as shoulder stability, proprioception, strength, and scapular control. The trial will be conducted at a single elite handball academy, including six teams (three male, three female) in the U16-U20 age categories. Teams will be randomised at the cluster level (team) into one of two intervention arms, each performing one of the two prevention programmes for the entire competitive half-season (18 weeks).

Unlike most injury prevention studies in adolescent athletes, this trial combines weekly self-reported monitoring of shoulder health (OSTRC-O Shoulder Module) with a comprehensive battery of objective, instrumented assessments of shoulder function, scapular control, strength, and proprioception. This dual approach allows for a more precise evaluation of programme effectiveness, capturing both perceived and measurable physical changes.

This prevention trial forms part of a larger, ongoing research programme investigating shoulder function and return-to-sport readiness following shoulder injury in overhead athletes. The same battery of objective tests (scapular dyskinesis assessment, LSST, mLSST, CKCUEST, YBT-UQ, proprioception testing, isometric strength testing) used here is also applied in the broader project, allowing the present study to generate insights that directly inform both preventive strategies and post-injury rehabilitation protocols.

The findings from this trial are expected to inform refinements of existing shoulder injury prevention protocols, enhance compliance strategies, and support sport-specific adaptations for adolescent elite handball players and other overhead athletes.

Study Timeline

• Status Verified: 2025-08
• Study Start: 2025-08-01
• Study First Submitted: 2025-08-13
• Study First Submitted QC: 2025-08-21
• Study First Posted: 2025-08-28
• Last Update Submitted: 2025-09-01
• Last Update Posted: 2025-09-08
• Primary Completion: 2025-12-22
• Study Completion: 2025-12-22

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 137

Inclusion Criteria

• Registered competitive handball players from the participating academy team (U16, U18, U20; male and female).
• Age between 13 and 19 years at baseline assessment.
• Currently participating in regular handball training and matches (minimum 3 training sessions per week).
• Member of a team assigned to the intervention for the full study period.
• Provided written informed consent (and parental consent for participants under 18 years).

Exclusion Criteria

• Acute shoulder injury at baseline preventing training
• Shoulder surgery in last 6 months
• Contraindication to resistance training
• Concurrent enrolment in another interventional study targeting the shoulder/upper limb.
• Refusal of informed consent (and parental consent for participants <18 years).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Scapular Dyskinesis Test (SDT) - classification during flexion and abduction	Baseline and 18 weeks	Description: Standard Kibler/McClure SDT with five consecutive repetitions of active shoulder flexion and abduction at a metronome cadence. Participants hold hand weights scaled to body mass: 1.5 kg if body mass \<68.1 kg, and 2.5 kg if ≥68.1 kg. Testing is video-recorded. Two trained assessors, rate each shoulder from the videos as none / subtle / obvious dyskinesis for each plane. Primary outcome: proportion with any dyskinesis (subtle+obvious) by plane; secondary: shift in severity category from baseline. Lower prevalence/severity indicates improvement.; Rater reliability plan: Inter-rater agreement will be quantified using weighted Cohen's kappa per plane.
Change in Y Balance Test - Upper Quarter (composite reach, % limb length)	Baseline and 18 weeks	Description: YBT-UQ performed for each arm in three directions (medial, inferolateral, superolateral), three valid trials per direction. Composite reach score = (sum of the 3 maximal reaches / limb length) × 100. Limb length = C7 to tip of middle finger. Primary score is the composite % per arm; higher is better.
Shoulder proprioception error in external and internal rotation (absolute error, degrees)	Baseline and 18 weeks	Joint position sense was assessed in supine position using a wrist-mounted digital angle gauge. For external rotation testing, the participant actively moved the arm to their individual full external rotation in 90° abduction. The target angle was then calculated using the formula: (Full ER in degrees-90)/2+90 This yields a mid-range position between neutral and the individual's maximal external rotation.; First, with eyes open, then vision was occluded using a towel, and the procedure was repeated three times per limb: the assessor passively positioned the arm at the target, returned it to vertical, and the participant attempted to reposition it to the same angle without visual feedback.; The absolute repositioning error (in degrees) between the target and reproduced positions was recorded for each trial, then averaged across the three trials per limb.; Internal rotation target angle calculated as: 90-(90-Full IR in degrees)/2 Lower error values indicate better proprioceptive acuity
OSTRC-O Shoulder Module severity score (0-100)	Weekly for 18 Weeks	Weekly Oslo Sports Trauma Research Center Overuse Injury Questionnaire (4 items). Composite 0-100 severity (higher = worse). Report mean weekly severity, prevalence of any problem (non-minimum response on any item), and prevalence of substantial problem (moderate/severe reduction in training/performance or complete inability to participate), as per standard methodology.

Secondary Outcome Measures

Name	Time	Method
Change in CKCUEST performance (touch count)	Baseline and 18 weeks	Closed Kinetic Chain Upper Extremity Stability Test (CKCUEST). Participants assume a standard push-up position with two parallel tape lines placed at a distance equal to 1.5 × the participant's biacromial breadth (measured between the lateral edges of the acromion processes). They alternately touch the opposite hand with one hand for three trials of 15 seconds each, with 30 seconds rest.; Two outcomes are recorded: 1. Touch count - mean number of valid touches across the three trials (per participant). Higher values indicate better upper-extremity closed-chain stability and power.; 2. Error count - number of form faults (e.g., loss of plank, hip rotation \>45°, line misses) summed across the three trials. Lower values indicate better movement quality/control.; A trained assessor records both outcomes according to published protocols, flagging invalid repetitions and documenting errors in real time.
Lateral Scapular Slide Test (LSST) total asymmetry score (3 positions)	Baseline and 18 weeks	LSST performed by measuring the side-to-side difference (mm) in the distance between the inferior angle of the scapula (angulus inferior) and the nearest midline spinous process in three standardized arm positions: (1) arms relaxed at sides; (2) hands on hips with thumbs posterior; (3) 90° humeral abduction with internal rotation. The total LSST score is calculated as the sum of absolute asymmetries across the three positions. Lower scores indicate better scapular symmetry/control. Measurements are taken with a non-elastic, millimeter-scale measuring tape, with the athlete standing in a relaxed posture, feet shoulder-width apart.
Modified LSST (mLSST; 2 kg and 4 kg)	Baseline and 18 weeks	Modified Lateral Scapular Slide Test (mLSST) performed in a static 30° scaption position while holding dumbbells of 2 kg and 4 kg, respectively. For each load, the side-to-side difference (mm) between the inferior angle of the scapula (angulus inferior) and the nearest midline spinous process is measured using a non-elastic, millimeter-scale measuring tape. The outcome for each load is the absolute asymmetry (mm). Lower values indicate better scapular symmetry/control under load.
Change in isometric shoulder strength - external and internal rotation	Baseline and 18 weeks	Maximal isometric shoulder external rotation (ER) and internal rotation (IR) strength measured using a ForceFrame testing system (VALD Performance). Testing was performed in supine position with the shoulder in 90° abduction and neutral rotation. For each rotation direction, participants completed two maximal-effort trials per limb (due to time constraints; standard protocols recommend three), with \~30 seconds rest between trials.; The highest peak force (N) from the two trials was used for analysis. Participants received standardized verbal encouragement during each trial. The ForceFrame system was calibrated before testing and measurements were recorded according to manufacturer guidelines.
Training/match exposure (minutes per week)	Weekly for 18 Weeks	Self-reported weekly minutes of handball training, match play, and strength/conditioning. Used to adjust analyses and to compute injury rates (exploratory).
Programme adherence (sessions/week)	Weekly for 18 Weeks	Number of completed prevention sessions per week (team logs + player self-report). Outcome: mean sessions/week per athlete and per team; proportion achieving ≥2 sessions/week.
Programme compliance (perceived usefulness score)	Weekly for 18 Weeks	Weekly self-reported perception of the programme's usefulness on a 0-10 scale (0 = not useful at all, 10 = extremely useful). Report mean weekly score and trends over time. Used to explore the relationship between perceived usefulness and adherence.
Time-loss shoulder injury incidence (per 1,000 exposure hours) - exploratory	Up to 18 Weeks	Any acute or overuse shoulder complaint causing time-loss (missed full training/match), verified with staff logs. Rate = injuries / 1,000 h (training + match).
Adverse events related to prevention sessions	Up to 18 Weeks	Number and nature of adverse events (e.g., exacerbation of pain leading to missed session; other exercise-related events) recorded by staff.

Trial Locations

Locations (1)

FTC Handball Academy; 🇭🇺 Budapest, Hungary