Effectiveness of a Standardised Stabilisation Exercise Protocol in Volleyball Players With Non-traumatic Shoulder Instability

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorUniversidad Francisco de Vitoria

About this trial

This randomized controlled clinical trial aims to evaluate the effectiveness of a standardized shoulder stabilization exercise program in amateur volleyball players diagnosed with atraumatic shoulder instability. Shoulder pain is one of the most prevalent musculoskeletal complaints, affecting up to two-thirds of the general population at some point in life and frequently leading to long-term symptoms, functional limitations, sleep disturbances, and high socio-economic costs. Atraumatic glenohumeral instability is particularly common among athletes performing overhead movements, such as volleyball players, who are repeatedly exposed to high-velocity external and internal rotation actions during serves and spikes.

The Derby Shoulder Instability Rehabilitation Programme (DSIRP) is a structured, reproducible protocol integrating strengthening, proprioceptive, neuromuscular control, plyometric, and speed-oriented exercises. Although widely used in clinical practice, evidence supporting its superiority over the natural progression of the condition remains limited. More than 80% of physiotherapists in the United Kingdom do not use specific standardized protocols for atraumatic shoulder instability, highlighting the need for high-quality clinical trials that evaluate structured rehabilitation approaches.

This study will recruit amateur volleyball players aged 20 to 30 years with a clinical diagnosis of atraumatic shoulder instability lasting more than 3 months. Participants will be randomized (1:1) into two parallel groups: an experimental group performing the DSIRP for 8 weeks (three 25-minute sessions per week), and a control group following a "wait-and-see" approach. Outcome measures will be assessed at baseline, 1 month, and 2 months (post-intervention). The primary outcomes include pain intensity measured with the Numeric Pain Rating Scale and shoulder disability measured with the Spanish version of the Shoulder Pain and Disability Index. Secondary outcomes include external rotation strength, grip strength, shoulder range of motion, and health-related quality of life assessed with the SF-12 questionnaire. All measurements use validated instruments with high reliability for clinical and research settings.

Statistical analysis will follow an intention-to-treat approach using mixed-model repeated-measures ANOVA or non-parametric alternatives when appropriate. Effect sizes and Bonferroni correction for multiple comparisons will be applied. An independent biostatistician blinded to allocation will conduct the analysis. The study follows CONSORT and TIDieR guidelines for reporting and intervention description.

This trial seeks to determine whether a structured, progressive stabilization protocol offers clinically meaningful improvements in pain, disability, strength, mobility, and quality of life compared with no intervention in young volleyball players with atraumatic shoulder instability. Results may support the implementation of standardized rehabilitation strategies in physiotherapy practice for this condition.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Amateur volleyball players.

Age range: 18 to 30 years.

Clinical diagnosis of atraumatic shoulder instability.

Symptom duration greater than 3 months.

Disqualifiers

Previous surgeries on the affected shoulder.

Previous fractures of the affected shoulder.

History of traumatic shoulder dislocation.

Shoulder pain originating from cervical spine pathology.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Other intervention

    Participants assigned to the intervention group will complete the Derby Shoulder Instability Rehabilitation Programme (DSIRP), a structured and progressive exercise-based protocol specifically designed for individuals with atraumatic shoulder instability. The program integrates strengthening exercises, proprioceptive and neuromuscular control training, plyometric drills, and speed-oriented stabilization tasks. Progression through the exercises is criterion-based, following predefined functional milestones to ensure appropriate challenge and individualized adaptation. The DSIRP focuses on enhancing dynamic glenohumeral stability through rotator-cuff activation, scapular control, and kinetic-chain coordination. Each session includes components targeting isometric and isotonic strengthening, closed-chain stability tasks, rhythmic stabilization, rapid-response perturbation activities, and overhead-sport-specific movement patterns relevant to volleyball athletes.

Treatment groups

22 Participants
are divided into 2 treatment groups
Group A: ControlNo intervention 0 interventions
Group B: Intervention groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity

Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point numerical rating scale ranging from 0 ("no pain") to 10 ("worst imaginable pain"). The NPRS has demonstrated adequate test-retest reliability, with intraclass correlation coefficients (ICC) ranging from 0.63 to 0.92, and strong internal consistency, with Cronbach's alpha values between 0.84 and 0.98, as previously reported in studies evaluating its psychometric properties (Stratford \& Spadoni, 2001; Jensen \& McFarland, 1993; Jensen et al., 1986)

Time frame
From enrollment to the end of treatment at 8 weeks

Secondary outcomes

1

Shoulder disability

Shoulder disability will be assessed using the Spanish version of the Shoulder Pain and Disability Index (SPADI), a self-reported questionnaire designed to measure shoulder pain and functional limitations through 13 items originally developed by Williams et al. (1995). The instrument has demonstrated the ability to discriminate between patients who improve and those who worsen (Roy et al., 2009), and its Spanish cross-cultural adaptation preserves the original structure and psychometric properties, providing a reliable and valid patient-reported outcome measure suitable for both clinical practice and research (Membrilla-Mesa et al., 2015)

Time frame
From enrollment to the end of treatment at 8 weeks
2

External rotation strength

Isometric external rotation strength of the shoulder will be measured using the MicroFET 2 MT Digital Handheld Dynamometer (Hoggan Health Industries, West Draper, UT). Handheld dynamometry has shown good to excellent intra-examiner reliability for isometric shoulder strength assessment, with intraclass correlation coefficients ranging from 0.87 to 0.99, according to prior studies evaluating its reproducibility in clinical and research settings (McLaine et al., 2016; Holt et al., 2016)

Time frame
From enrollment to the end of treatment at 8 weeks
3

Hand grip strength

Hand grip strength will be measured using a Jamar handheld dynamometer (Sammons Preston Rolyan, Bolingbrook, IL), a device widely recognized for its robustness and reproducibility. This instrument has demonstrated good to excellent intra-examiner reliability for isometric grip strength outcomes, with intraclass correlation coefficients ranging from 0.85 to 0.98 in previous validation studies (Roberts et al., 2011)

Time frame
From enrollment to the end of treatment at 8 weeks
4

Shoulder mobility

Shoulder range of motion will be assessed for flexion, abduction, external rotation at 0°, external rotation at 90°, and internal rotation at 90° of abduction using a validated smartphone inclinometer application (Plaincode Software Solutions, Gunzenhausen, Germany). This tool has shown excellent inter-examiner reliability and validity in symptomatic individuals, with intraclass correlation coefficients greater than 0.80 for shoulder mobility measurements (Werner et al., 2014)

Time frame
From enrollment to the end of treatment at 8 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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