Comparison of Taping Techniques in Plantar Fasciitis
Primary Purpose
Plantar Fasciitis, Pain, Foot Diseases
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Extracorporeal Shockwave Therapy (ESWT)
Low-Dye Taping
Kinesio Taping
Sponsored by
About this trial
This is an interventional treatment trial for Plantar Fasciitis
Eligibility Criteria
Inclusion Criteria:
- Individuals diagnosed with plantar fasciitis by a physician
- Age between 18 and 30 years
- Agree to participate in the study
Exclusion Criteria:
- Not having surgery
- Disagree to participate in the study
- Infection
- Pregnancy
- Tumor
Sites / Locations
- KTO Karatay University
- Bayram Sönmez ÜNÜVAR
- KTO Karatay University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Low-Dye Taping
Kinesio Taping
Extracorporeal Shockwave Therapy (ESWT)
Arm Description
In addition to the ESWT applied to the participants in the control group, Low-Dye Taping will be applied to the participants in this group once a week for 3 sessions.
In addition to the ESWT applied to the participants in the control group, Kinesio Taping will be applied to the participants in this group once a week for 3 sessions.
Participants in the control group will receive 3 sessions of ESWT once a week.
Outcomes
Primary Outcome Measures
Change from baseline in Pain at 3 Session
A visual analog scale (VAS) numbered 0-10 will be used in the assessment of pain.
Change from baseline in Pain at 3 Session
In functional evaluation, the scale developed by The American Orthopaedic Foot & Ankle Society (AOFAS) will be used.
Secondary Outcome Measures
Full Information
NCT ID
NCT05592808
First Posted
October 20, 2022
Last Updated
March 28, 2023
Sponsor
KTO Karatay University
1. Study Identification
Unique Protocol Identification Number
NCT05592808
Brief Title
Comparison of Taping Techniques in Plantar Fasciitis
Official Title
Comparison of the Effects of Low-Dye and Kinesio Taping Methods in Plantar Fasciitis
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
October 24, 2022 (Actual)
Primary Completion Date
March 20, 2023 (Actual)
Study Completion Date
March 27, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
KTO Karatay University
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
The aim of this study is to investigate the effects of Low-Dye and Kinesio Taping on pain and function in individuals with plantar fasciitis.
Detailed Description
Subject: In this study, the effects of Low-Dye Taping and Kinesio Taping (KT) on pain and function will be investigated in individuals with plantar fasciitis. There are studies on both Low-Dye banding and KT in the literature and they are popular applications recently. However, to the best of our knowledge, when we look at the Turkish and English literature, no study has been found comparing these two therapeutic massages in terms of pain, functionality and performance.
Purpose: Plantar fasciitis (PF) is a clinical picture characterized by degeneration of the plantar fascia resulting from repetitive microtrauma to the plantar fascia causing an inflammatory reaction. It is one of the most common causes of heel pain in adults. The plantar fascia has a fundamental role in the biomechanics of the foot, supporting the medial longitudinal arch (MLA), distributing forces and stresses of the foot during gait or other loading conditions. Disorders in the musculoskeletal and somatosensory system in patients with plantar fasciitis may cause pain and decrease in functional capacity. Therefore, its purpose is; This study was planned to show the effectiveness of taping methods applied in addition to ESWT in individuals presenting with heel pain. Thanks to the findings to be obtained from our study, it is aimed to contribute to the literature with objective, evidence-based results in this field.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fasciitis, Pain, Foot Diseases
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
45 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Low-Dye Taping
Arm Type
Experimental
Arm Description
In addition to the ESWT applied to the participants in the control group, Low-Dye Taping will be applied to the participants in this group once a week for 3 sessions.
Arm Title
Kinesio Taping
Arm Type
Experimental
Arm Description
In addition to the ESWT applied to the participants in the control group, Kinesio Taping will be applied to the participants in this group once a week for 3 sessions.
Arm Title
Extracorporeal Shockwave Therapy (ESWT)
Arm Type
Active Comparator
Arm Description
Participants in the control group will receive 3 sessions of ESWT once a week.
Intervention Type
Device
Intervention Name(s)
Extracorporeal Shockwave Therapy (ESWT)
Intervention Description
Extracoporeal shock wave, 2000 shots/time, once a week for 3 weeks, shock wave freqency: 10Hz, total energy: 166 mJ/mm2, Pressure 2.5 Bar
Intervention Type
Other
Intervention Name(s)
Low-Dye Taping
Intervention Description
After ESWT application, Low-Dye Taping will be applied 3 times, once a week.
Intervention Type
Other
Intervention Name(s)
Kinesio Taping
Intervention Description
After ESWT application, Kinesio Taping will be applied 3 times, once a week.
Primary Outcome Measure Information:
Title
Change from baseline in Pain at 3 Session
Description
A visual analog scale (VAS) numbered 0-10 will be used in the assessment of pain.
Time Frame
Changes in the VAS scores of the three groups before the treatment
Title
Change from baseline in Pain at 3 Session
Description
In functional evaluation, the scale developed by The American Orthopaedic Foot & Ankle Society (AOFAS) will be used.
Time Frame
Changes in the AOFAS scores of the three groups before the treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Individuals diagnosed with plantar fasciitis by a physician
Age between 18 and 30 years
Agree to participate in the study
Exclusion Criteria:
Not having surgery
Disagree to participate in the study
Infection
Pregnancy
Tumor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bayram Sönmez ÜNÜVAR
Organizational Affiliation
KTO Karatay University
Official's Role
Principal Investigator
Facility Information:
Facility Name
KTO Karatay University
City
Konya
ZIP/Postal Code
42020
Country
Turkey
Facility Name
Bayram Sönmez ÜNÜVAR
City
Konya
ZIP/Postal Code
42250
Country
Turkey
Facility Name
KTO Karatay University
City
Konya
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
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Comparison of Taping Techniques in Plantar Fasciitis
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