NCT07190768

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
5mo left

Started Oct 2025

Status
not yet recruiting

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 Progress60%
Oct 2025Oct 2026

First Submitted

Initial submission to the registry

September 17, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 24, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2026

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Expected
Last Updated

September 24, 2025

Status Verified

September 1, 2025

Enrollment Period

3 months

First QC Date

September 17, 2025

Last Update Submit

September 23, 2025

Conditions

Keywords

Kinesiologic tapingshoulder paindry needling

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

EXPERIMENTAL
Other: Kinesio TapingBehavioral: Exercise Program

Dry Needling + Exercise

EXPERIMENTAL
Other: Dry NeedlingBehavioral: Exercise Program

Kinesio Taping + Dry Needling + Exercise

EXPERIMENTAL
Other: Kinesio TapingOther: Dry NeedlingBehavioral: Exercise Program

Conventional Physical Therapy + Exercise (Control)

ACTIVE COMPARATOR
Behavioral: Exercise ProgramDevice: Conventional Physical Therapy (TENS/Ultrasound/Heat pack)

Interventions

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.

Kinesio Taping + Dry Needling + ExerciseKinesio Taping + Exercise

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).

Dry Needling + ExerciseKinesio Taping + Dry Needling + Exercise

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.

Conventional Physical Therapy + Exercise (Control)Dry Needling + ExerciseKinesio Taping + Dry Needling + ExerciseKinesio Taping + Exercise

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.

Conventional Physical Therapy + Exercise (Control)

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Shoulder PainShoulder Impingement Syndrome

Interventions

Dry NeedlingResistance Training

Condition Hierarchy (Ancestors)

ArthralgiaJoint DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsShoulder InjuriesWounds and Injuries

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeuticsPhysical Therapy ModalitiesExercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CarePhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Central Study Contacts

Erkan Kaya, Associate Prof.

CONTACT

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