- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05384236
A Comparative Study of Kinesiology Taping Versus Taping in the Treatment of Plantar Fasciitis (Taping)
Plantar fasciitis is a very studied pathology and treated with taping. There are studies that assess the effectiveness of Kinesio taping, as well as taping or low-dye taping, few studies that compare the two treatments and assess which is more effective.
In the present work the effectiveness of Kinesio taping and taping will be assessed, as well as whether possible differences among intervention effects exist in terms of pain improvement, comfort and durability of the bandage.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Valencia, Spain, 46010
- Universitat de València
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- People with plantar fasciitis.
- People of legal age.
Exclusion Criteria:
- Healthy people
- Minors.
- People with pathologies other than plantar fasciitis in the foot.
- People who have treatment for fasciitis at the time of starting the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: kinesiology taping
Application of a neuromuscular bandage on the plantar fascia
|
To apply kinesiology taping in plantar fascia
|
|
ACTIVE_COMPARATOR: taping or Low-dye taping
Application of a taping on the plantar fascia
|
To apply taping or Low-dye taping in plantar fascia
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale of Pain
Time Frame: seven days
|
It is rated on a scale of 0 to 10, where 0 is no pain and 10 is extreme pain.
|
seven days
|
|
comfort
Time Frame: seven days
|
Comfort is rated on a scale of 0 to 10, where 0 is no comfotable and 10 is very comfortable
|
seven days
|
|
Visual Analogue Scale of Mobility
Time Frame: seven days
|
the degree of MOBILITY that the foot has had when using the bandage, rated from 0 no mobility to 10
|
seven days
|
|
Visual Analogue Scale of comfort
Time Frame: seven days
|
The degree of COMFORT IN HYGIENE of the bandage: (for example at the time of showering or personal hygiene), rated from 0, no comfort to 10, maximum confort
|
seven days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UNIVERSIDAD DE VALENCIA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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