NCT05779033

Brief Summary

studying the effect of ultrasound and kinesiotaping in shoulder impingement syndrome in reliefing pain and increase range of motion in subjects with shoulder impingement syndrome .

Trial Health

87
On Track

Trial Health Score

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

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 9, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

March 22, 2023

Completed
18 days until next milestone

Study Start

First participant enrolled

April 9, 2023

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 8, 2023

Completed
Last Updated

November 19, 2025

Status Verified

November 1, 2025

Enrollment Period

5 months

First QC Date

March 9, 2023

Last Update Submit

November 17, 2025

Conditions

Keywords

ultrasoundkinesiotapingShoulder Impingement Syndromeshoulder painshoulder range of motion

Outcome Measures

Primary Outcomes (4)

  • severity of pain

    Assessed By visual analogue scale (VAS) , The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health) orientated from the left (worst) to the right (best).

    4 weeks

  • Range Of Motion

    assessed By Digital Goniometer

    4 weeks

  • Function

    assessed by disability of arm and hand quick questionnaire (quick DASH).

    4 weeks

  • Hand strength

    assessed by hand dynamometer.

    4 weeks

Study Arms (3)

control group

PLACEBO COMPARATOR

will receive scapular stabilization exercises 3 times per week for 4 weeks.

Behavioral: scapular stabilization exercises

study group (A)

ACTIVE COMPARATOR

will receive scapular stabilization exercises and Kinesiotape 3 times per week for 4 weeks

Behavioral: scapular stabilization exercisesOther: Kinesio Tape

study group (B)

ACTIVE COMPARATOR

will receive scapular stabilization exercises and Ultrasound 3 times per week for 4 weeks.

Behavioral: scapular stabilization exercisesDevice: ultrasound

Interventions

scapular stabilization exercises 3 times per week for 4 weeks.

control groupstudy group (A)study group (B)

Ultrasound 3 times per week for 4 weeks.continuous US operated at a frequency of 1 MHz and at an intensity of 1.5 W/cm2 for 5 minutes

Also known as: US
study group (B)

Kinesiotape 3 times per week for 4 weeks. We will apply taping to two muscles (deltoideus and supraspinatus). A "Y' tape was placed over the deltoid muscle using the muscle stimulation (KT strip arms were located by stretching slightly by 15%-25%) and mechanical correction techniques (KT strip arms were located with maximal stretching). Another "Y" tape was placed over the supraspinatus muscle using the muscle inhibition technique (the starting point of the tape was attached to the sub acromial-greater tubercle with submaximal (75%) stretching and without stretching on strip arms).

Also known as: KT
study group (A)

Eligibility Criteria

Age20 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients with shoulder impingement syndrome from both genders their age will be ranged and divided into three groups from 20-50 years.
  • History of shoulder pain for one month.
  • Positive Neer's impingement test and Hawkin's kiennedy test.
  • Provocation of pain above 60 degrees of flexion and abduction.

You may not qualify if:

  • History of Shoulder girdle fracture, dislocation and surgery
  • Diagnosed with frozen shoulder or rotator cuff tear
  • History of cervicobrachial pain
  • Any neuromuscular pain in upper limb and use of corticosteroids or pain subsiding medication

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mahmoud Ahmed Kashef

Cairo, Cairo Governorate, 0325, Egypt

Location

Related Publications (2)

  • Letafatkar A, Rabiei P, Kazempour S, Alaei-Parapari S. Comparing the effects of no intervention with therapeutic exercise, and exercise with additional Kinesio tape in patients with shoulder impingement syndrome. A three-arm randomized controlled trial. Clin Rehabil. 2021 Apr;35(4):558-567. doi: 10.1177/0269215520971764. Epub 2020 Nov 6.

  • Gunay Ucurum S, Kaya DO, Kayali Y, Askin A, Tekindal MA. Comparison of different electrotherapy methods and exercise therapy in shoulder impingement syndrome: A prospective randomized controlled trial. Acta Orthop Traumatol Turc. 2018 Jul;52(4):249-255. doi: 10.1016/j.aott.2018.03.005. Epub 2018 Apr 25.

Related Links

MeSH Terms

Conditions

Shoulder Impingement SyndromeShoulder Pain

Interventions

UltrasonographyAthletic Tape

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and InjuriesArthralgiaPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosisBandagesEquipment and SuppliesOrthotic DevicesOrthopedic EquipmentSurgical Equipment

Study Officials

  • Hassan hu ahmed, professor

    Cairo University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Patients with shoulder impingement syndrome from both genders will participate in this study after approval of ethical committee of the faculty of physical therapy, Cairo University, and all participants provided written informed consent. Sample size: estimate 45 patients until we measure power analysis The subjects will be arranged into three groups: * Group I (control group) will receive scapular stabilization exercises 3 times per week for 4 weeks. * Group II will receive scapular stabilization exercises and Kinesiotape 3 times per week for 4 weeks. * Group III will receive scapular stabilization exercises and Ultrasound 3 times per week for 4 weeks.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
B.SC physical therapy

Study Record Dates

First Submitted

March 9, 2023

First Posted

March 22, 2023

Study Start

April 9, 2023

Primary Completion

September 1, 2023

Study Completion

October 8, 2023

Last Updated

November 19, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will share

(age-severity of pain-range of motion function level of shoulder joint)'s of patients will be shared

Shared Documents
ICF
Time Frame
4 weeks
Access Criteria
paper concent

Locations