Effect of Kinesio Taping on Upper Extremity Performance in Individuals With Rounded Shoulders

November 20, 2023 updated by: Mahidol University
The objective of this research is to study the effect of kinesio tapes with functional correction technique in combination with exercise management to increase strength and decrease pain, in people with rounded shoulders. The study would be evaluated with the EvaltechTM machine, (functional capacity assessment).

Study Overview

Detailed Description

Participants

  • Age 25-50 years, male and female
  • People who have a shoulder condition. (By measuring in the supine position, distance from the posterior aspect of acromion to the bed> 1 inch on both sides)
  • People with moderate to severe neck and shoulder pain (VAS> 3)
  • People who have to use their arms for work Overall more than 3 hours per day

For attaching the tape, the researcher will prepare a replacement shirt in case the For the convenience of tape, the experimental group, trained by Certified Kinesio tape, attached the kinesio tape. Attaching the tape By using functional correction techniques, apply from the front of the acromion process to the spinous process T10 on both sides.

Measurements

  1. The pressure of (average of peak force) of both arms (pounds)
  2. The pulling force (average of peak force) of both arms (pounds)
  3. Time of overhead endurance test (TMT) (seconds)
  4. Visual analog scale (VAS)
  5. The distance from the posterior aspect of acromion to the bed (inches)

process of measuring the evaluation 3 times

  1. st after physical therapy treatment Before attaching the kinase tape
  2. nd evaluation period was 48 hours apart before the next treatment.
  3. rd evaluation period is 1 week apart.

Study Type

Interventional

Enrollment (Actual)

26

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Nakhonpathom
      • Salaya, Nakhonpathom, Thailand, 73170
        • Mahidol University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age 25-50 years, male and female
  • People who have a shoulder condition. (By measuring in the supine position, distance from the posterior aspect of acromion to the bed> 1 inch on both sides)
  • People with moderate to severe neck and shoulder pain (VAS> 3)
  • People who have to use their arms for work Overall more than 3 hours per day

Exclusion Criteria:

  • People with neck pain, fracture in the arm, and numbness
  • People who have pain and have limited shoulder movement of the shoulder joint
  • People who have had a history of spine / shoulder surgery
  • People with a history of allergies to cloth tapes
  • People who have rheumatoid arthritis that affects inflammation of the joints such as rheumatoid etc.
  • People receiving medication that affects their participation in the study
  • People with neurological symptoms
  • People with cognitive disabilities

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Kinesio tape, functional correction applying
The experimental group, trained by Certified Kinesio tape researcher will attache the kinesio tape. Attaching the kinesio tape by using functional correction techniques, apply tape from the front of the acromion process to the spinous process T10 on both sides, providing 50% of the tape's tension (Kase, 2003, Han JT et al) to create a scapular retraction.
According to Kinesio Taping, functional correction technique could use for correcting shoulder, scapular alignment and decrease pain.

The exercise in which both groups will receive Introduction of exercise with rubber bands (Elastic band) It is a home exercise (Home base exercise program) for patients to do with appropriate resistance. Which can be done at least 10 times and not more than 20 times continuously,will be asked to do all 3 positions.

1) Shoulder external rotation in shoulder abduction 90 degrees 2) Shoulder horizontal abduction in shoulder abduction 90 degrees 3) Seated bend row, which will be done 15 times, each hold for 10 seconds, do 3 sets, each set rest 2 minutes, 2 times a day ( Morning-evening) consecutively for 1 week

Placebo Comparator: Placebo Kinesio taping apply
Apply kinesio tape without tension.

The exercise in which both groups will receive Introduction of exercise with rubber bands (Elastic band) It is a home exercise (Home base exercise program) for patients to do with appropriate resistance. Which can be done at least 10 times and not more than 20 times continuously,will be asked to do all 3 positions.

1) Shoulder external rotation in shoulder abduction 90 degrees 2) Shoulder horizontal abduction in shoulder abduction 90 degrees 3) Seated bend row, which will be done 15 times, each hold for 10 seconds, do 3 sets, each set rest 2 minutes, 2 times a day ( Morning-evening) consecutively for 1 week

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The pushing force (average of peak force) of both arms (pounds)
Time Frame: 2 minutes
Maximum strength of pushing, measures by Evaltech machine
2 minutes
The pulling force (average of peak force) of both arms (pounds)
Time Frame: 2 minutes
Maximum strength of pulling, measures by Evaltech machine
2 minutes
Time measurement tolerance (TMT) (seconds)
Time Frame: 4 minutes
Time tolerance of overhead reaching, measures by Evaltech machine
4 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual analog pain scale (VAS)
Time Frame: 1 minute
0-10 centimeters visual analog scale, higher score means higher pain and worse outcome
1 minute
The distance from the posterior aspect of acromion to the bed (inches)
Time Frame: 2 minutes
Measure in lying position by measurement tape
2 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Prasert Sakulsriprasert, PhD, Lecturer

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 7, 2021

Primary Completion (Actual)

May 1, 2023

Study Completion (Actual)

May 31, 2023

Study Registration Dates

First Submitted

April 11, 2020

First Submitted That Met QC Criteria

April 11, 2020

First Posted (Actual)

April 15, 2020

Study Record Updates

Last Update Posted (Estimated)

November 21, 2023

Last Update Submitted That Met QC Criteria

November 20, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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