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Effectiveness of Neuromuscular Kinesiology Taping in Plantar Fasciitis

Primary Purpose

Fasciitis, Plantar

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Kinesiotaping
Tape
Sponsored by
University of Valencia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fasciitis, Plantar

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Universitat de València

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

kinesiotaping

Tape

Arm Description

Outcomes

Primary Outcome Measures

Visual Analogue Scale of Pain
A visual analogue scale of pain will assess from 0, no pain, to 10, the worst possible pain

Secondary Outcome Measures

Bandage durability
Period of time in days from when the bandage is put on until it comes off

Full Information

First Posted
March 22, 2022
Last Updated
November 16, 2022
Sponsor
University of Valencia
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1. Study Identification

Unique Protocol Identification Number
NCT05328700
Brief Title
Effectiveness of Neuromuscular Kinesiology Taping in Plantar Fasciitis
Official Title
Effectiveness of Neuromuscular Kinesiology Taping in Plantar Fasciitis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
April 15, 2022 (Actual)
Primary Completion Date
October 29, 2022 (Actual)
Study Completion Date
October 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Valencia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fasciitis, Plantar

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
kinesiotaping
Arm Type
Experimental
Arm Title
Tape
Arm Type
Placebo Comparator
Intervention Type
Other
Intervention Name(s)
Kinesiotaping
Intervention Description
Perform a neuromuscular bandage with kinesiotape in patients with plantar fasciitis
Intervention Type
Other
Intervention Name(s)
Tape
Intervention Description
Perform a neuromuscular bandage with tape (Hipofix(R)) in patients with plantar fasciitis
Primary Outcome Measure Information:
Title
Visual Analogue Scale of Pain
Description
A visual analogue scale of pain will assess from 0, no pain, to 10, the worst possible pain
Time Frame
Change from baseline (before intervention) to one day, two days, three days and four days after intervention
Secondary Outcome Measure Information:
Title
Bandage durability
Description
Period of time in days from when the bandage is put on until it comes off
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

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Universitat de València
City
València
State/Province
Valencia
ZIP/Postal Code
46010
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Effectiveness of Neuromuscular Kinesiology Taping in Plantar Fasciitis

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