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Clinical Trial NCT07072091 (FocusVolley) for Shoulder Pain, Volleyball Players is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
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Focusing the Shoulder or Considering the Whole-Body in Volleyball Physiotherapy (FocusVolley) 40
Clinical Trial NCT07072091 (FocusVolley) is an interventional study for Shoulder Pain, Volleyball Players that is recruiting. It started on 20 July 2025 with plans to enroll 40 participants. Led by University of Trieste, it is expected to complete by 1 September 2025. The latest data from ClinicalTrials.gov was last updated on 14 August 2025.
Brief Summary
Shoulder pain can be common in overhead sports, and in particular, in volleyball. Different physiotherapy protocols can be adopted depending on the suspected pathophysiological mechanisms. Despite most of the protocols rely only on the shoulder district, some research suggests that treating the whole-body might produce better results as it could influence kinematic chains and correct muscle imbalances. The aim of thi...Show More
Official Title
Focusing the Shoulder or Considering the Whole-Body? A Randomized Controlled Trial on Physiotherapy Protocols for the Painful Shoulder in Volleyball Players
Conditions
Shoulder PainVolleyball PlayersPublications
Scientific articles and research papers published about this clinical trial:Other Study IDs
- FocusVolley
- DSM_Fisio_SpallaPallavolo25
NCT ID Number
Start Date (Actual)
2025-07-20
Last Update Posted
2025-08-14
Completion Date (Estimated)
2025-09
Enrollment (Estimated)
40
Study Type
Interventional
PHASE
N/A
Status
Recruiting
Primary Purpose
Treatment
Design Allocation
Randomized
Interventional Model
Parallel
Masking
Double
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
No InterventionHealthy controls A convenience sample of healthy volleyball players for cross-sectional comparison | N/A |
ExperimentalTotal body physiotherapy group Physiotherapy intervention consisting in whole body exercise and treatment | Total body physiotherapy This intervention consists in 5 weeks of 2 x week 60 min sessions of physiotherapy consisting in active exercise performed in upper limb, trunk, and lower limb muscles, in a whole-body approach. |
Active ComparatorFocus shoulder group Physiotherapy intervention consisting in shoulder exercise and treatment | Focus shoulder physiotherapy This intervention consists in 5 weeks of 2 x week 60 min sessions of physiotherapy consisting in active exercise performed only in the shoulder district, focusing on the trunk-arm muscles. |
OtherNo physiotherapy group No physiotherapy, only education | Education Single education session providing information about posture hygiene and proper warm-up |
Primary Outcome Measures
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Isometric strength with handheld dynamometer (Newtons) | Isometric strength during shoulder flexion, extension, external and internal rotation, bilaterally | At enrollment and at the end of treatment at 5 weeks |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Lateral symmetry (%) | Lateral symmetry will be assessed as percentage between the two upper limbs for the investigated muscles (pectoralis major, latissimus dorsi, upper trapezius, middle trepezius, lower trapezius, anterior deltoid, posterior deltoid) using the tensiomyography system | At enrollement and at the end of treatment after 5 weeks |
Time of contraction (ms) | Time of contraction (ms), i.e. the time requiring the muscle to reach the peak of muscle displacement, will be assessed as percentage between the two upper limbs for the investigated muscles (pectoralis major, latissimus dorsi, upper trapezius, middle trepezius, lower trapezius, anterior deltoid, posterior deltoid) using the tensiomyography system | At enrollement and at the end of treatment after 5 weeks |
Muscle belly displacement (mm) | Muscle belly displacement (mm), i.e. the amplitude of muscle displacement, will be assessed as percentage between the two upper limbs for the investigated muscles (pectoralis major, latissimus dorsi, upper trapezius, middle trepezius, lower trapezius, anterior deltoid, posterior deltoid) using the tensiomyography system | At enrollement and at the end of treatment after 5 weeks |
Participation Assistant
Eligibility Criteria
Eligible Ages
Child, Adult
Minimum Age
17 Years
Eligible Sexes
All
Accepts Healthy Volunteers
Yes
- practicing volleyball for at least 5 years with a training volume of minimum 5 h/wk
- history of previous surgical intervention or fractures on the shoulder or spine
Study Responsible Party
Alex Buoite Stella, Principal Investigator, PhD, Assistant professor, University of Trieste
No contact data.
1 Study Locations in 1 Countries
Trieste
University of Trieste - Exercise Physiology and Kinesiology Lab, Trieste, Trieste, 34100, Italy
Alex Buoite Stella, PhD, Contact, 0039 0403996582, [email protected]
Recruiting