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Clinical Trials/NCT06706531
NCT06706531
Recruiting
Not Applicable

Additional Effects of Dry Needling With Conventional Physical Therapy Versus Conventional Physical Therapy in Plantar Fasciitis: a Randomized Control Trial

Foundation University Islamabad1 site in 1 country44 target enrollmentJune 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Plantar Fascitis
Sponsor
Foundation University Islamabad
Enrollment
44
Locations
1
Primary Endpoint
Pain intensity
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This study is a randomized controlled trial and the purpose of this study is to determine the effects of dry needling with conventional physical therapy versus conventional physical therapy on gait parameters in plantar fasciitis: a randomized control trial.

Detailed Description

The purpose of this study is to determine the effects of dry needling with conventional physical therapy versus conventional physical therapy on gait parameters in plantar fasciitis Outcomes variables of Pain , Ankle ROM, gait parameters and activities of daily living in adults (age : 40-60 years ) will be determined using: 1. Numeric pain rating scale 2. Goniometer 3. 30 meter walk test 4. foot and ankle ability measure FAAM Data will be before and after the intervention protocol for each participant. Data collection procedure: Participants of interest would be approached and explained about the research. Informed written consent will be taken. Pre and post intervention scores will be recorded.

Registry
clinicaltrials.gov
Start Date
June 1, 2024
End Date
December 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Pain intensity

Time Frame: 3 weeks

Pain will be measured on Numerical Pain rating scale. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable").

The Foot and Ankle Ability Measure (FAAM)

Time Frame: 3 weeks

It is a self-report outcome instrument developed to assess physical function for individuals with foot and ankle related impairments .The response to each item on the ADL subscale is scored from 4 to 0, with 4 being 'no difficulty' and 0 being 'unable to do'

Gait speed:

Time Frame: 3 weeks

Gait speed = Distance (m) / time (s)

Cadence

Time Frame: 3 weeks

Cadence (steps/min) = steps counted x 60 / time (s)

Cycle length

Time Frame: 3 weeks

Cycle time (s) = time (s) x 2/steps counted

Stride length

Time Frame: 3 weeks

SL (m) = speed (m/s) x cycle time (s)

Range of motion

Time Frame: 3 weeks

Ankle range will be measured with goniometer

Study Sites (1)

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