Skip to content

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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07190768
Enrollment
100
Registered
2025-09-24
Start date
2025-10-01
Completion date
2026-10-01
Last updated
2025-09-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder Impingement Syndrome, Shoulder Pain

Keywords

Kinesiologic taping, shoulder pain, dry needling

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.

Interventions

OTHERKinesio Taping

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.

OTHERDry Needling

Participants received dry needling (DN) applied with sterile, disposable stainless-steel needles (0.30 mm × 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).

BEHAVIORALExercise Program

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.

DEVICEConventional Physical Therapy (TENS/Ultrasound/Heat pack)

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.

Sponsors

Bursa City Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Pain intensity (Visual Analogue Scale, VAS)Baseline, immediately after first treatment, 1 week after first treatment, and at the end of week 3.

Secondary

MeasureTime frame
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.

Contacts

Primary ContactErkan Kaya, Associate Prof.
doktorerkankaya@yahoo.com+905056719830

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026