- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06533683
Effects of Kinesio Taping and Extracorporeal Shock Wave Therapy in the Calcaneal Spur
Effects of Kinesio Taping Versus Extracorporeal Shock Wave Therapy on Pain in the Treatment of Calcaneal Spur: A Retrospective Clinical Study
The term "heel pain" is used to describe a common, painful condition that is localized in the plantar part of the heel and worsens when weight is placed on the heel. Patients with heel pain are more likely to have thickened plantar fascia, abnormal plantar fascia tissue, thicker plantar heel fat pad, and calcaneal spur. Calcaneal spurs are bony protrusions that typically occur just in front of the medial calcaneal tuberosity. Systemic medical treatments, physical therapy agents, exercise and local injections are often applied for heel pain caused by plantar fasciitis and calcaneal spur.
This study is to examine the effects of ESWT and kinesio taping on pain and other clinical outcomes in patients with calcaneal spurs.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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İstanbul, Turkey
- Sisli Hamidiye Etfal Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged 18 years and over with heel pain
- A calcaneal spur seen on foot radiographs
Exclusion Criteria:
- Those who had received a steroid injection into the heel within the past three months
- Those who had experienced trauma or surgery to the foot and ankle within the past six months
- Those with a rheumatic disease affecting the foot and ankle (e.g., spondyloarthritis)
- Those with open wounds or infections in the area to be treated with lesions.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Group 1 : ESWT treatment group
ESWT treatment is applied once a week for 5 weeks
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Group 2 : Kinesio taping treatment group
Kinesio taping was also applied once a week, for a total of 5 sessions.
The rake method was used for kinesio taping.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain level before treatment and 3rd month after treatment
Time Frame: From enrollment to the end of treatment at 3rd month
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Pain level will be evaluated with the Numerical Rating Scale.
(minimum: 0, maximum: 10)
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From enrollment to the end of treatment at 3rd month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Assessment of heel sensitivity
Time Frame: From enrollment to the end of treatment at 3rd month
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It will be evaluated with the Heel Tenderness index.
(0=no pain; 1=painful; 2=painful and whines; 3=painful, whines, and withdraws)
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From enrollment to the end of treatment at 3rd month
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Assessment of functionality
Time Frame: From enrollment to the end of treatment at 3rd month
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Foot Function Index was used.
The FFI consists of 23 items divided into 3 subscales that quantify the impact of foot pathology on pain, disability, and activity limitation in patients.
Pain, disability, and activity limitation subscale scores range from 0 to 100.
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From enrollment to the end of treatment at 3rd month
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Assessment of quality of life
Time Frame: From enrollment to the end of treatment at 3rd month
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The 12-item short-form health survey (SF-12) quality of life scale was used to evaluate general quality of life.
It was presented as a physical component score (PCS) and mental component score (MCS).
Scores range from 0 to 100, with higher scores indicating better physical and mental health functioning.
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From enrollment to the end of treatment at 3rd month
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Collaborators and Investigators
Investigators
- Study Director: Banu Kuran, Professor, Sisli Hamidiye Etfal Training and Research Hospital
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
- 26.09.2023 / 4096
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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