NCT05592808

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 20, 2022

Completed
4 days until next milestone

Study Start

First participant enrolled

October 24, 2022

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 25, 2022

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2023

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 27, 2023

Completed
Last Updated

March 30, 2023

Status Verified

October 1, 2022

Enrollment Period

5 months

First QC Date

October 20, 2022

Last Update Submit

March 28, 2023

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change from baseline in Pain at 3 Session

    A visual analog scale (VAS) numbered 0-10 will be used in the assessment of pain.

    Changes in the VAS scores of the three groups before the treatment

  • 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.

    Changes in the AOFAS scores of the three groups before the treatment

Study Arms (3)

Low-Dye Taping

EXPERIMENTAL

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.

Device: Extracorporeal Shockwave Therapy (ESWT)Other: Low-Dye Taping

Kinesio Taping

EXPERIMENTAL

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.

Device: Extracorporeal Shockwave Therapy (ESWT)Other: Kinesio Taping

Extracorporeal Shockwave Therapy (ESWT)

ACTIVE COMPARATOR

Participants in the control group will receive 3 sessions of ESWT once a week.

Device: Extracorporeal Shockwave Therapy (ESWT)

Interventions

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

Extracorporeal Shockwave Therapy (ESWT)Kinesio TapingLow-Dye Taping

After ESWT application, Low-Dye Taping will be applied 3 times, once a week.

Low-Dye Taping

After ESWT application, Kinesio Taping will be applied 3 times, once a week.

Kinesio Taping

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Individuals diagnosed with plantar fasciitis by a physician
  • Age between 18 and 30 years
  • Agree to participate in the study

You may not qualify if:

  • Not having surgery
  • Disagree to participate in the study
  • Infection
  • Pregnancy
  • Tumor

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

KTO Karatay University

Konya, 42020, Turkey (Türkiye)

Location

Bayram Sönmez ÜNÜVAR

Konya, 42250, Turkey (Türkiye)

Location

KTO Karatay University

Konya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Fasciitis, PlantarPainFoot Diseases

Interventions

Extracorporeal Shockwave Therapy

Condition Hierarchy (Ancestors)

FasciitisMusculoskeletal DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsSkin DiseasesSkin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Ultrasonic TherapyDiathermyHyperthermia, InducedTherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Officials

  • Bayram Sönmez ÜNÜVAR

    KTO Karatay University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 20, 2022

First Posted

October 25, 2022

Study Start

October 24, 2022

Primary Completion

March 20, 2023

Study Completion

March 27, 2023

Last Updated

March 30, 2023

Record last verified: 2022-10

Data Sharing

IPD Sharing
Will not share

Locations