Effects of Kinesio Taping and Extracorporeal Shock Wave Therapy in the Calcaneal Spur

July 30, 2024 updated by: Selda Çiftci, Sisli Hamidiye Etfal Training and Research Hospital

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

Completed

Detailed Description

The responses of patients who underwent ESWT or kinesio taping due to calcaneal spur before and after treatment will be compared. Pain, functionality and quality of life are the clinical parameters compared.

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • İstanbul, Turkey
        • Sisli Hamidiye Etfal Training and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Patients who applied to the Physical Medicine and Rehabilitation outpatient clinic of Şişli Hamidiye Etfal Training and Research Hospital with complaints of heel pain were evaluated. The data of patients who underwent ESWT and kinesio taping were compared with the information on the hospital system.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Group 1 : ESWT treatment group
ESWT treatment is applied once a week for 5 weeks
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain level before treatment and 3rd month after treatment
Time Frame: From enrollment to the end of treatment at 3rd month
Pain level will be evaluated with the Numerical Rating Scale. (minimum: 0, maximum: 10)
From enrollment to the end of treatment at 3rd month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of heel sensitivity
Time Frame: From enrollment to the end of treatment at 3rd month
It will be evaluated with the Heel Tenderness index. (0=no pain; 1=painful; 2=painful and whines; 3=painful, whines, and withdraws)
From enrollment to the end of treatment at 3rd month
Assessment of functionality
Time Frame: From enrollment to the end of treatment at 3rd month
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.
From enrollment to the end of treatment at 3rd month
Assessment of quality of life
Time Frame: From enrollment to the end of treatment at 3rd month
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.
From enrollment to the end of treatment at 3rd month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Banu Kuran, Professor, Sisli Hamidiye Etfal Training and Research Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2023

Primary Completion (Actual)

February 1, 2024

Study Completion (Actual)

March 1, 2024

Study Registration Dates

First Submitted

July 30, 2024

First Submitted That Met QC Criteria

July 30, 2024

First Posted (Actual)

August 1, 2024

Study Record Updates

Last Update Posted (Actual)

August 1, 2024

Last Update Submitted That Met QC Criteria

July 30, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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