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Clinical Trials/NCT05754697
NCT05754697
Completed
Not Applicable

Instrument Assisted Soft Tissue Mobilization Versus Positional Release Technique in Patients With Chronic Plantar Fasciitis

Cairo University1 site in 1 country60 target enrollmentMarch 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Plantar Fasciitis
Sponsor
Cairo University
Enrollment
60
Locations
1
Primary Endpoint
Pressure Algometer (Change in pain pressure threshold)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial] is to compare between the effect of instrument assisted soft tissue mobilization and positional release technique in patients with chronic plantar fasciitis

The main question[s] it aims to answer are:

  1. Is there a difference between the effect of instrument assisted soft tissue mobilization and positional release technique on pain pressure threshold in patients with chronic plantar fasciitis?
  2. Is there a difference between the effect of instrument assisted soft tissue mobilization and positional release technique on foot function level in patients with chronic plantar fasciitis?

Detailed Description

Design of the study: Pretest - posttest randomized controlled trial. Subjects selection: Sixty patients their age range from 30-50 years of both genders with chronic plantar fasciitis will participate in this study according to sample size calculation.

Registry
clinicaltrials.gov
Start Date
March 15, 2023
End Date
July 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Doaa Said Mohamed Ibrahim

Assistant Lecturer

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Clinically diagnosed cases of plantar fasciitis not less than 3 months.
  • Heel pain felt maximally over plantar aspect of heel.
  • Pain in the heel on the first step in the morning.
  • Their age ranging from 30-50 years.
  • Body mass index range from (18.5 to 24.9 kg/m2).

Exclusion Criteria

  • Subjects can't tolerate close physical contact.
  • Subjects with skin infections.
  • Subjects with recent fracture with incomplete bony union.
  • Subjects with acute inflammatory or infectious process.
  • Subjects with hematoma.
  • Subjects with osteoporosis.
  • Subjects with foot deformity.
  • Subjects that take medications that may increase blood clotting.
  • Surgery to the ankle or foot.

Outcomes

Primary Outcomes

Pressure Algometer (Change in pain pressure threshold)

Time Frame: Pre-intervention and immediately after intervention

Change in pain pressure threshold as assessed using pressure algometer on medial plantar process, with the unit of measurement in kg/cm². Change in pain pressure threshold as assessed using pressure algometer on gastrocnemius muscle, with the unit of measurement in kg/cm². Change in pain pressure threshold as assessed using pressure algometer on soleus muscle, with the unit of measurement in kg/cm². Change in pain pressure threshold as assessed using pressure algometer over the posteromedial aspect of the calcaneus , with the unit of measurement in kg/cm².

Secondary Outcomes

  • The Arabic Version of Foot and Ankle Ability Measure(Pre-intervention and immediately after intervention)

Study Sites (1)

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