Immediate Effects of Flossband and Mobilization With Movement on Shoulder Mobility in Volleyball Athletes
Comparison of the Immediate Effect of Flossband and Mobilization With Movement on Shoulder Mobility in Volleyball Athletes: A Randomized Clinical Trial
1 other identifier
interventional
36
1 country
1
Brief Summary
The goal of this clinical trial is to learn if Floss Band application works as effectively as mobilization with movement (MWM) to improve shoulder mobility in volleyball athletes. It will also explore whether these techniques affect athletes' perception of movement fluency and sport-specific performance. The main questions it aims to answer are: Does Floss Band application immediately improve shoulder range of motion in volleyball athletes? Does Floss Band application change the perception of movement fluency compared to MWM? Does Floss Band application impact sport-specific performance tests compared to MWM? Participants will: Be randomly assigned to receive either Floss Band or mobilization with movement Have their shoulder mobility, perception of movement, and sport performance tested before and immediately after the intervention
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2025
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
First Submitted
Initial submission to the registry
September 9, 2025
CompletedFirst Posted
Study publicly available on registry
September 25, 2025
CompletedStudy Start
First participant enrolled
October 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 18, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 18, 2026
CompletedSeptember 25, 2025
September 1, 2025
6 months
September 9, 2025
September 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Shoulder Range of Motion - External Rotation
Glenohumeral external rotation (dominant shoulder) will be measured using the Baseline® Digital Inclinometer. The participant will lie in the supine position with the shoulder abducted to 90°, elbow flexed to 90°, and forearm in neutral. The inclinometer will be placed on the anterior mid-forearm, and the participant will perform active external rotation. Three measurements will be taken, and the mean value will be calculated for analysis.
Baseline (prior to intervention, Day 1) and post-intervention (Day 1)
Shoulder Range of Motion - Internal Rotation, Flexion, Abduction, Horizontal Abduction
Internal rotation: same supine position, inclinometer on posterior mid-forearm. Flexion and abduction: seated with hips, knees, and ankles at 90° flexion; inclinometer on anterior humerus for flexion, lateral mid-humerus for abduction. Horizontal abduction: supine, shoulder 90° abduction, 90° external rotation, elbow 90° flexion; inclinometer on anterior mid-humerus. Three measurements per movement will be recorded and averaged.
Baseline (prior to intervention, Day 1) and post-intervention (Day 1)
Secondary Outcomes (3)
Functional Performance - One-arm Seated Single Arm Shot Put Test (OSP)
Baseline (prior to intervention, Day 1) and post-intervention (Day 1)
Functional Throwing Performance Index (FTPI)
Baseline (prior to intervention, Day 1) and post-intervention (Day 1)
Perceived Movement Fluency (VAS)
Immediately post-intervention (Day 1)
Study Arms (2)
Mobilization with Movement (MWM) Group
ACTIVE COMPARATORParticipants in this arm will perform the standardized Mobilization with Movement (MWM) protocol. While seated in a chair with back support and hips, knees, and ankles at 90° flexion, the researcher will stabilize the scapula with one hand and apply a posterolateral glide to the anterior humeral head with the other hand during active shoulder elevation in the scapular plane. The intervention consists of 3 sets of 10 repetitions, with a 1-minute rest interval between sets. Assessments will be conducted at baseline and immediately post-intervention, including shoulder range of motion using a digital inclinometer, perception of movement fluency using a Visual Analogue Scale (VAS), and sport-specific performance tests (One-arm Seated Shot Put Test and Functional Throwing Performance Index).
Floss Band Group (FBG)
EXPERIMENTALParticipants in this arm will perform the standardized Floss Band (FBG) protocol. While seated with the shoulder at 90° abduction, the researcher will apply a compressive elastic band made of 100% polymer gel (T.P.E), measuring 210 cm in length, 5 cm in width, and 1.3 mm in thickness. The first anchor is placed two fingers medial to the acromion, and the band is wrapped around the shoulder until the second anchor at the end of the band is fixed. After the application, the participant will perform sport-specific movements (spike and serve) for 2 minutes. Following the completion of the compression period, the band will be removed. Assessments will be conducted at baseline and immediately post-intervention, including shoulder range of motion using a digital inclinometer, perception of movement fluency using a Visual Analogue Scale (VAS), and sport-specific performance tests (One-arm Seated Shot Put Test and Functional Throwing Performance Index).
Interventions
Participants in this arm will perform the standardized Floss Band (FBG) protocol. While seated with the shoulder at 90° abduction, the researcher will apply a compressive elastic band made of 100% polymer gel (T.P.E), measuring 210 cm in length, 5 cm in width, and 1.3 mm in thickness. The first anchor is placed two fingers medial to the acromion, and the band is wrapped around the shoulder until the second anchor at the end of the band is fixed. After the application, the participant will perform sport-specific movements (spike and serve) for 2 minutes. Following the completion of the compression period, the band will be removed. Assessments will be conducted at baseline and immediately post-intervention, including shoulder range of motion using a digital inclinometer, perception of movement fluency using a Visual Analogue Scale (VAS), and sport-specific performance tests (One-arm Seated Shot Put Test and Functional Throwing Performance Index).
Participants in this arm will perform the standardized Mobilization with Movement (MWM) protocol. While seated in a chair with back support and hips, knees, and ankles at 90° flexion, the researcher will stabilize the scapula with one hand and apply a posterolateral glide to the anterior humeral head with the other hand during active shoulder elevation in the scapular plane. The intervention consists of 3 sets of 10 repetitions, with a 1-minute rest interval between sets. Assessments will be conducted at baseline and immediately post-intervention, including shoulder range of motion using a digital inclinometer, perception of movement fluency using a Visual Analogue Scale (VAS), and sport-specific performance tests (One-arm Seated Shot Put Test and Functional Throwing Performance Index).
Eligibility Criteria
You may qualify if:
- Age between 18 and 50 years.
- Male or female volleyball athletes (indoor or beach), at amateur or professional level.
- Regular training routine of at least two sessions per week.
- No shoulder pain at the time of testing or during the previous three months.
You may not qualify if:
- History of shoulder surgery, structural shoulder injuries (e.g., fractures, labrum tear), or recurrent glenohumeral dislocation.
- Skin disorders contraindicating the intervention, including active dermatitis, inflammatory-phase psoriasis, cutaneous infections (e.g., folliculitis), open wounds, burns, eczema, or hypersensitivity in the shoulder region.
- Vascular disorders contraindicating the intervention, including history or diagnosis of deep vein thrombosis, symptomatic varicose veins, peripheral arterial disease, lymphedema, or advanced chronic venous insufficiency.
- Other conditions contraindicating intervention: peripheral neuropathies with significant sensory loss, presence of a pacemaker in the region of band application, known allergy to elastic band material, or pain during shoulder movement at assessment.
- Development of shoulder or elbow injuries during the study, especially requiring surgical intervention.
- Participants who voluntarily withdraw from the study at any time.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Federal University of Paraíba
Igarapé-Açu, Pará, 58051-900, Brazil
Related Publications (27)
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PMID: 33837162BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Researcher, and Principal Investigator (PhD), Federal University of Paraíba
Study Record Dates
First Submitted
September 9, 2025
First Posted
September 25, 2025
Study Start
October 20, 2025
Primary Completion
April 18, 2026
Study Completion
April 18, 2026
Last Updated
September 25, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ANALYTIC CODE
- Time Frame
- IPD and supporting information will be made available starting 6 months after publication of the main study results and will remain accessible for 5 years.
- Access Criteria
- Data will be shared with qualified researchers upon request. Researchers must submit a data access request and sign a data use agreement outlining the intended analyses and ensuring confidentiality. Requests will be reviewed by the principal investigator to ensure that proposed use aligns with the study objectives and ethical standards.
Individual participant data (IPD) collected in this study, including de-identified measurements of shoulder range of motion, functional performance tests, and perceived movement fluency, will be made available to other researchers. Data dictionaries describing each variable, coding, and units will also be provided. Sharing will occur in accordance with participant consent, ethical approvals, and data privacy regulations, after the publication of the main study results.