- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05328700
Effectiveness of Neuromuscular Kinesiology Taping in Plantar Fasciitis
One of the pathologies most studied and treated with kinesiotape (KT) is plantar fasciitis (PF). In most of the studies reviewed, it is concluded that there is an improvement in the symptoms of PF when treated with KT: either combined with other therapies or as a single treatment compared to placebo. However, most current studies have limitations because the sample is small, the effect size is small, and the evidence is insufficient or of low quality.
In the present work, the aim is to study the effectiveness of KT in PF, and to compare the results with those obtained in a placebo group, which is treated with tape. The researchers will assess the decrease in symptoms prior to performing other definitive treatments. In addition, the variability of the painful symptoms and the durability of the bandage will be studied, in order to determine whether it can be used in the short or long period of time, being able to take it into account and supposing a supplement to the pharmacological treatment.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Valencia
-
València, Valencia, Spain, 46010
- Universitat de València
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- People with acute plantar fasciitis with less than 3 months of evolution
- Who present pain in the fascia both during ambulation and on palpation
- Ecographic image compatible with plantar fasciitis (> 4 mm)
- The condition has not be previously treated with other treatment
Exclusion Criteria:
- Condition with no sintomatology
Study Plan
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: kinesiotaping
|
Perform a neuromuscular bandage with kinesiotape in patients with plantar fasciitis
|
|
Placebo Comparator: Tape
|
Perform a neuromuscular bandage with tape (Hipofix(R)) in patients with plantar fasciitis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale of Pain
Time Frame: Change from baseline (before intervention) to one day, two days, three days and four days after intervention
|
A visual analogue scale of pain will assess from 0, no pain, to 10, the worst possible pain
|
Change from baseline (before intervention) to one day, two days, three days and four days after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bandage durability
Time Frame: Change from baseline (the bandage is put on) until the first day that the loss of the bandage is documented, assessed up to 7 days
|
Period of time in days from when the bandage is put on until it comes off
|
Change from baseline (the bandage is put on) until the first day that the loss of the bandage is documented, assessed up to 7 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
- VNM_CC
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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