- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02367157
Effectiveness of Kinesio Tape in Morning Stiffness and Functional Capacity in Patients With Rheumatoid Arthritis.
February 19, 2021 updated by: CEU San Pablo University
The purpose of this study is to determine how the applications of Kinesio Tape affect the morning stiffness in patients with rheumatoid arthritis.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
20
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 Locations
-
-
Madrid
-
Boadilla del Monte, Madrid, Spain, 28668
- San Pablo CEU 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
40 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Diagnosis of Rheumatoid Arthritis according to the criteria of the American Rheumatism Association with a minimum of 6 months evolution from diagnosis.
- These subjects must have morning stiffness daily in the wrist joint of a member or bilateral at least a month.
Exclusion Criteria:
- Subjects in postoperative affecting the mobility of joints to study phase.
- Subjects with sensory deficits or other inflammatory arthropathies.
- Subjects who are or come in a state of emergence of the hand or wrist joints during the investigation.
- Subjects who change their usual treatment (medication or other therapies) two months before the study or during the study.
- We exclude subjects who present some kind of allergy to Kinesio-Tape in which case it will be removed immediately.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental: Kinesio taping
Epicondilar and epitroclear muscle Kinesio Taping with a Space Correction on the wrist according Kenzo Kase Method
|
|
|
No Intervention: No intervention: Control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in the Wrist Morning Stiffness
Time Frame: participants will be followed for the duration in minutes of the morning stiffness, an expected average of 45 minutes]
|
participants will be followed for the duration in minutes of the morning stiffness, an expected average of 45 minutes]
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
March 1, 2016
Primary Completion (Actual)
May 1, 2017
Study Completion (Actual)
June 1, 2017
Study Registration Dates
First Submitted
February 13, 2015
First Submitted That Met QC Criteria
February 19, 2015
First Posted (Estimate)
February 20, 2015
Study Record Updates
Last Update Posted (Actual)
February 21, 2021
Last Update Submitted That Met QC Criteria
February 19, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- CEU-009
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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