Effectiveness of Kinesiologic Taping and Dry Needling in the Treatment of Subacromial Pain Syndrome
The Comparison of the Effectiveness of Kinesiologic Taping and Dry Needling in the Treatment of Subacromial Pain Syndrome: a Randomize Trial
1 other identifier
interventional
100
0 countries
N/A
Brief Summary
This study aims to compare the effectiveness of two common physiotherapy methods, Kinesiologic Taping (KT) and Dry Needling (DN), in the treatment of Subacromial Pain Syndrome (SAPS), a frequent cause of shoulder pain. The trial also investigates whether using KT and DN together provides greater benefits than using them separately. The main goal is to determine which treatment approach is more effective in reducing pain and improving shoulder function in patients with SAPS.
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 Oct 2025
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 17, 2025
CompletedFirst Posted
Study publicly available on registry
September 24, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2026
ExpectedSeptember 24, 2025
September 1, 2025
3 months
September 17, 2025
September 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain intensity (Visual Analogue Scale, VAS)
Baseline, immediately after first treatment, 1 week after first treatment, and at the end of week 3.
Secondary Outcomes (2)
Shoulder function (Quick-DASH questionnaire)
Baseline, 1 week after first treatment, and at the end of week 3.
Kinesiophobia (Tampa Scale of Kinesiophobia, TSK-19)
Baseline, 1 week after first treatment, and at the end of week 3.
Study Arms (4)
Kinesio Taping + Exercise
EXPERIMENTALDry Needling + Exercise
EXPERIMENTALKinesio Taping + Dry Needling + Exercise
EXPERIMENTALConventional Physical Therapy + Exercise (Control)
ACTIVE COMPARATORInterventions
Participants received Kinesio Taping (KT) applied to the affected shoulder using standard 5-cm Kinesio Tex tape. Before application, an allergy test was performed by placing a small patch of tape on the contralateral forearm for 15 minutes. The taping procedure included three regions: supraspinatus muscle, deltoid muscle, and glenohumeral joint. Application technique: Supraspinatus: Y-strip applied from insertion on the greater tubercle along the muscle to its origin with 20-25% stretch. Deltoid: Y-strip applied from 3 cm below insertion to the origin, with anterior and posterior tails placed along corresponding edges. Glenohumeral joint: I-strip applied from the coracoid process, laterally under the acromion, around the posterior deltoid edge. Schedule: Tape was applied at baseline (Day 0), reapplied at Day 7, and removed permanently at Day 14.
Participants received dry needling (DN) applied with sterile, disposable stainless-steel needles (0.30 mm Ă— 50 mm). Target muscles included the supraspinatus, deltoideus, infraspinatus, subscapularis, and pectoralis major. Technique: The "fast-in, fast-out" method (Hong technique) was used. After cleaning the skin with alcohol, the needle was inserted into a palpable taut band until the first local twitch response (LTR) was elicited. The needle was moved vertically (5-10 mm) at \~1 Hz for 25-30 seconds. DN was applied for 45-60 seconds per muscle. Schedule: Twice per week, for 3 weeks (total of 6 sessions).
All participants were instructed in a standardized home-based exercise program designed to improve shoulder mobility and stability. Content: Exercises included active range-of-motion movements, scapular stabilization, and strengthening of rotator cuff and periscapular muscles. Ergonomic advice and posture correction were also provided. Delivery: Participants were taught the program in person and instructed to perform the exercises at home. Schedule: Exercises were performed daily for 3 weeks, in addition to the assigned intervention for each study arm.
Participants in this arm received conventional physical therapy modalities commonly used for the management of subacromial pain syndrome. Modalities: Transcutaneous electrical nerve stimulation (TENS), therapeutic ultrasound, or superficial heat pack were applied based on standard clinical practice. Additional care: Sessions also included passive mobilization of the shoulder into end range, scapular stabilization exercises, and ergonomic/postural advice. Schedule: One-hour treatment sessions, 5 days per week, for 3 consecutive weeks.
Eligibility Criteria
You may qualify if:
- Age 18-65 years
- Pain in the upper, outer arm, especially during shoulder elevation
- Shoulder pain lasting more than 6 weeks with or without partial rotator cuff tear
- At least three of the following findings:
- Painful arc during flexion or abduction
- Positive Neer test
- Positive Hawkins-Kennedy test
- Painful resisted external rotation
- Positive Jobe's test
- Diagnosis confirmed by MRI evaluation when indicated
You may not qualify if:
- Participation in a physical therapy program or receipt of injection therapy within the past 3 months
- Previous shoulder surgery
- Presence of joint contracture
- Complete tendon rupture
- Cervical radiculopathy
- Systemic inflammatory disease (e.g., rheumatoid arthritis, ankylosing spondylitis)
- Known allergy to tape or materials used in interventions
- Bleeding disorders
- Local infection or open wound in the treatment area
- Cognitive dysfunction that prevents cooperation
- History of malignancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc. Prof
Study Record Dates
First Submitted
September 17, 2025
First Posted
September 24, 2025
Study Start
October 1, 2025
Primary Completion
January 1, 2026
Study Completion (Estimated)
October 1, 2026
Last Updated
September 24, 2025
Record last verified: 2025-09