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Clinical Trials/NCT04346563
NCT04346563
Completed
Not Applicable

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

Mahidol University1 site in 1 country26 target enrollmentJanuary 7, 2021
ConditionsShoulder Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Pain
Sponsor
Mahidol University
Enrollment
26
Locations
1
Primary Endpoint
The pushing force (average of peak force) of both arms (pounds)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

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).

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.

Registry
clinicaltrials.gov
Start Date
January 7, 2021
End Date
May 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

The pushing force (average of peak force) of both arms (pounds)

Time Frame: 2 minutes

Maximum strength of pushing, measures by Evaltech machine

The pulling force (average of peak force) of both arms (pounds)

Time Frame: 2 minutes

Maximum strength of pulling, measures by Evaltech machine

Time measurement tolerance (TMT) (seconds)

Time Frame: 4 minutes

Time tolerance of overhead reaching, measures by Evaltech machine

Secondary Outcomes

  • Visual analog pain scale (VAS)(1 minute)
  • The distance from the posterior aspect of acromion to the bed (inches)(2 minutes)

Study Sites (1)

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