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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01991171
Other study ID # CAAE14385813.1.0000.5512
Secondary ID 250.259
Status Completed
Phase N/A
First received November 18, 2013
Last updated October 21, 2014
Start date May 2013
Est. completion date November 2013

Study information

Verified date October 2014
Source Paulista University
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

Forty-eight female patients will be randomized into three groups to receive the Kinesio taping, placebo Kinesio taping and control group. The group Kinesio taping receive the correct application of the method described. The placebo group will receive a placement without tension. The control group did not receive any form of intervention.


Description:

The group Kinesio taping receive the correct application of the method described with tension of 40%. The placebo group will receive a placement without tension.

The control group did not receive any form of intervention.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date November 2013
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria:

- Woman

- Sedentary

Exclusion Criteria:

- Physically active,

- pain

- men

- musculoskeletal injury in the last six months.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Kinesio Taping
Kinesiotaping intervention is based upon the use of specific elastic tapes (known as Kinesio Tex Gold) that are applied with a certain amount of tension fixed to the skin of patients with the target muscles in a stretched position. The tapes will be placed over the quadriceps muscle.

Locations

Country Name City State
Brazil Universidade Paulista Jundiaí São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Paulista University

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vertical Jump The vertical jump will be evaluated by the Counter Movement Jump 40 minutes No
Secondary Flexibility The flexibility will be evaluate by fleximeter 40 minutes No
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