Comparison of Two Different Treatment Methods

Comparison of Short-term Effects of Two Different Treatment Methods in Patients With Subacromial Impingement Syndrome: a Randomized Controlled Single-blind Trial

A number of previous studies investigated the effects of kinesiotaping (KT) in subacromial impingement syndrome (SIS).

Study Overview

• Status: Completed
• Conditions: Musculoskeletal Diseases; Musculoskeletal Pain; Subacromial Impingement Syndrome; Musculoskeletal Injury; Weakness, Muscle
• Intervention / Treatment: Other: Kinesiotaping; Other: Mulligan Mobilization Technique

Detailed Description

Subacromial impingement syndrome (SIS) is characterized by shoulder pain that is exacerbated with especially arm elevation or overhead physical activities.

• Study Type: Interventional
• Enrollment (Actual): 60
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Turkey
  • Muğla, Turkey, 48000
    • Muğla Sıtkı Kocman University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 31 years to 61 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Impingement symptoms in clinical tests
• Pain >1 month

Exclusion Criteria:

• Any shoulder pathology.
• Have chronic systemic diseases or infections.
• History of any surgery shoulder complex.
• steroid injections and therapeutic approaches

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
No Intervention: Control Group (CG); Control group
Experimental: Kinesiotaping Group (KG); Experimental group	Other: Kinesiotaping; KT was applied.
Experimental: Mulligan Mobilization Technique Group (MG); Experimental group (2)	Other: Mulligan Mobilization Technique; MMT was applied

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of pain severity	Via VAS.	Baseline- after 2 weeks (after treatment)
Change of Range of Motion	Via goniometer.	Baseline- after 2 weeks (after treatment)
Change of Functionality	Via SPADI.	Baseline- after 2 weeks (after treatment)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of Sleep Quality	Via VAS.	Baseline- after 2 weeks (after treatment)
Change of Satisfaction of Life	Via SWLS.	Baseline- after 2 weeks (after treatment)
Change of Satisfaction of Treatment	Via VAs.	Baseline- after 2 weeks (after treatment)

Collaborators and Investigators

• Sponsor: Banu BAYAR
• Collaborators: Muğla Sıtkı Koçman University

Study record dates

Study Major Dates

• Study Start (Actual): September 28, 2021
• Primary Completion (Actual): October 15, 2021
• Study Completion (Actual): November 30, 2021

Study Registration Dates

• First Submitted: September 28, 2021
• First Submitted That Met QC Criteria: September 28, 2021
• First Posted (Actual): October 8, 2021

Study Record Updates

• Last Update Posted (Actual): December 21, 2022
• Last Update Submitted That Met QC Criteria: December 19, 2022
• Last Verified: December 1, 2022

More Information

Terms related to this study

• Keywords: Subacromial Impingement Syndrome; Physiotherapy; Kinesiotaping; Mulligan Mobilization Technique
• Additional Relevant MeSH Terms: Pathologic Processes; Nervous System Diseases; Pain; Neurologic Manifestations; Wounds and Injuries; Disease; Joint Diseases; Muscular Diseases; Rupture; Shoulder Injuries; Tendon Injuries; Neuromuscular Manifestations; Syndrome; Rotator Cuff Injuries; Muscle Weakness; Shoulder Impingement Syndrome; Musculoskeletal Pain; Musculoskeletal Diseases
• Other Study ID Numbers: 180030/16

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No