The Effectiveness of Kinesio Taping in Violin Players
1 other identifier
interventional
117
1 country
1
Brief Summary
This study aimed to investigate the effectiveness of Kinesio taping (KT) on playing-related pain, upper extremity and hand function, grip and pinch strength in violin players. One hundred seventeen participants who were professional violinists for at least two years were randomized to receive either therapeutic tape application (KT group), a sham tape application (placebo group) or no application (control group) for one week. The primary outcome was the Disabilities of the Arm, Shoulder and Hand (DASH) in one week. The secondary outcomes were the Visual Analogue Scale (VAS), the Purdue Pegboard Test, grip and pinch strength. Outcome measures were performed at baseline, immediately after the intervention, and one week later (follow-up). Participants were asked to play the "Violin Concerto No.2, Op.35", and pre-and post-performance pain and grip and pinch strength were assessed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2017
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
Study Start
First participant enrolled
September 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2018
CompletedFirst Submitted
Initial submission to the registry
August 15, 2021
CompletedFirst Posted
Study publicly available on registry
August 25, 2021
CompletedOctober 8, 2024
August 1, 2021
2 months
August 15, 2021
October 5, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Upper extremity function
The Disabilities of the Arm, Shoulder and Hand score is a self-administered questionnaire designed to evaluate single or multiple disorders and impairment levels in the upper limbs. It comprises 30 core questions and optional eight questions, which are scored on a 5-point Likert scale (no difficulty - unable). The cumulative score is ranged from 0 to 100, where the higher scores indicate an increased degree of disability.
Baseline
Secondary Outcomes (16)
Upper extremity function
Follow-up (one week later)
Playing-related pain
Baseline
Playing-related pain
Immediately after the intervention
Playing-related pain
Follow-up (one week later)
Playing-related pain
After one-week intervention (before playing Violin Concerto No.2, Op.35)
- +11 more secondary outcomes
Study Arms (3)
KT group
EXPERIMENTALParticipants were received single session therapeutic tape application for one week.
Placebo group
PLACEBO COMPARATORParticipants were received single session placebo tape application for one week.
Control group
NO INTERVENTIONNo intervention.
Interventions
Tape was applied to sternocleidomastoid, upper trapezius, deltoid, flexor palmaris longus muscles as suggested by Kase et al. (Kase, Wallis, Kase, \& Association, 2003). The tape was applied to the left side of the participants while sitting position because the violin is traditionally played by placing it on the left shoulder, balancing the neck using the left hand, and bowing with the right arm.
The placebo tape was applied transverse to the muscle groups in two levels (a point of 10 cm above to wrist and elbow) with no tension when the participants were sitting position with the shoulder flexed at 90°, and the elbow flexed at 90°.
Eligibility Criteria
You may qualify if:
- aged between 18 and 35 years;
- professionally playing violin at least for two years;
- having playing-related musculoskeletal pain at neck and upper extremity \[Visual Analogue Scale (VAS) ≥3\]
- ability to read and write in Turkish; and
- able to follow simple instructions.
You may not qualify if:
- having significant musculoskeletal, neurologic, or cardiovascular disorders;
- a history of surgery on the upper limbs in the previous six months;
- the initiation of any analgesic intervention for musculoskeletal pain within the previous six weeks;
- known allergies to tape; and
- participation in physiotherapy and rehabilitation program in the last six months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul University-Cerrahpasa
Istanbul, Bakırkoy, 34147, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Ebru Kaya Mutlu, PT, PhD
Istanbul University - Cerrahpasa
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
August 15, 2021
First Posted
August 25, 2021
Study Start
September 1, 2017
Primary Completion
November 1, 2017
Study Completion
March 31, 2018
Last Updated
October 8, 2024
Record last verified: 2021-08
Data Sharing
- IPD Sharing
- Will not share