The Effects of Dynamic Taping With Exercise on Neuromuscular Control in Individuals With Subacromial Impingement
NCT ID: NCT05957952
Last Updated: 2025-05-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
NA
50 participants
INTERVENTIONAL
2023-11-22
2025-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: This is a randomized control trial. Fifty individuals with SIS will be randomly assigned into either an exercise group or dynamic tape with exercise group. Both groups will receive 5 sessions of treatment in 2 weeks, with 30 minutes per sessions. Outcomes will be measured at baseline, after the first intervention and following 2-week intervention. Primary outcome measures will include scapular kinematics, scapular muscle activation and corticospinal system. Secondary outcome measures included shoulder pain by a numeric pain rating scale and shoulder function by the disability of the arm, shoulder \& hand scale (DASH). Data analysis: two-way and three-way mixed ANOVA will used to compare the intervention effect of two groups.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effects of Short-term Scapular Control Training in Overhead Athletes With Shoulder Impingement Syndrome
NCT04493190
Kinesio Taping Compared to Exercise Intervention for Round Shoulder Subjects With Impingement Syndrome
NCT03413488
Effects of Dynamic Taping on Shoulder Isokinetics Strength and Muscle Fatigue.
NCT06580925
Dynamic Taping in Symptomatic Rotator Cuff Tendinopathy
NCT05029544
Therapeutic Approaches for Subjects With Scapula Dyskinesis
NCT03252444
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exercise group
Motor control exercise
Motor control exercise
Subjects will learn how to control their scapula during motor control exercise without taping
Dynamic taping with exercise group
Motor control exercise combined with dynamic taping
Motor control exercise with dynamic taping
Subjects will learn how to control their scapula during motor control exercise with application of dynamic tape
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Motor control exercise with dynamic taping
Subjects will learn how to control their scapula during motor control exercise with application of dynamic tape
Motor control exercise
Subjects will learn how to control their scapula during motor control exercise without taping
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. The participants were only included if they were aged between 20-40 years.
3. Total participation time in shoulder exercises per week is greater than or equal to 4 hours.
4. Presence of scapular movement dysfunction.
5. Presence of shoulder impingement symptoms, with at least 3 positive results in the following 6 tests:
* Painful arc test
* Neer's impingement test
* Hawkins-Kennedy impingement test
* Empty can test
* Resisted external rotation test
* Tenderness of the rotator cuff tendons
Exclusion Criteria
2. Arm elevation angle less than 120 degrees
3. Have a history of dislocation, fracture, or surgery of upper extremity
4. A history of direct contact injury to the neck or upper extremities within the past 12 months
5. A concussion within the past 12 months or a history of three or more concussions
6. Brain injury and neurological impairment
7. History of frequent headache or dizziness
8. Contraindications to the use of transcranial magnetic stimulation, assessed with a safety screening questionnaire, including pregnancy, history of seizure, epilepsy and syncope, having cochlear implant, having medal implant and taking anti-depressant medication.
20 Years
40 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Yang Ming Chiao Tung University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yin-Liang Lin
Assistant Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Yang Ming Chiao Tung University
Taipei, Taiwan, Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NYCU112007AF
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.