- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06534866
"Effects of Kinesio Taping in Adjunct to Traditional Physical Therapy on Pain, Range of Motion and Gait Parameters in Patients With Plantar Fasciitis : a Randomized Controlled Trail"
"Effects of Kinesio Taping in Adjunct to Traditional Physical Therapy on Pain, Range of Motion and Gait Parameters in Patients With Plantar Fascitis : a Randomized Controlled Trail"
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The purpose of this study is to determine the difference between efffects of KInesio taping combined with traditional physical versus physical therapy alone.
The individual of Age 20-40 years among both genders and are diagnosed cases of plantar fasciitis Pain levels will be assessed using the Numeric Pain Rating Scale (NPRS). ROM will be assessed through goniometry. Gait parameters will be assessed through 30 meter walk test. Participants of interest would be approached and explained about the research. Informed written consent will be taken. It is a single-blinded study and randomization will be done through coin toss method. Both groups will receive conventional intervention. Additionally, Group B will receive kinesio taping treatment. Baseline and post intervention scores would be recorded for both groups.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Fatima Shakeel, MS-MSKPT*
- Phone Number: 03255784552
- Email: shakeefatima@gmail.com
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Recruiting
- Foundation University College of Physical Therapy
-
Contact:
- Ruqia Begum, MS-OMPT
- Phone Number: 03115532544
- Email: ruqia@fui.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both genders
- Age 20-40 years
- Diagnosed Cases of plantar fasciitis as per diagnosis criteria established by APTA
As described by American Physical Therapy Association:
Plantar medial heel pain: most noticeable with initial steps after a period of inactivity but also worse following prolonged weight bearing
- Heel pain precipitated by a recent increase in weight-bearing activity
- Pain with palpation of the proximal insertion of the plantar fascia
- Positive windlass test
- Negative tarsal tunnel tests
- Limited active and passive talocrural joint dorsiflexion range of motion
- Abnormal Foot Posture Index score
Exclusion criteria:
- Recent steroid injections
- History of ankle or foot surgery
- Arthritis history
- Radiculopathy
- Diabetic foot
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Traditional Physcial therapy group
|
|
|
Experimental: Kinesio taping + Traditional physical therapy group
Group B will receive :
(30 minutes session thrice a week for 2 consecutive weeks with total of 6 sessions) |
In the first step, after the metatarsophalangeal joints is dorsiflexed, the first strap will be adhered firmly to the posterior heel at its proximal end.
The other end of the strap is cut into four slices of equal width.
Each slice is applied with a 50% stretch (50% tensile strain) and attached to the plantar forefoot.
In the second step, another strap is applied with gentle compression across the bases of the four slices beneath the foot and wrapped around the rearfoot
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: 2 weeks
|
Pain is assessed by using numeric main rating scale comparing pre and post pain intensity.
This is 11- point numeric scale ranges from '0' representing one pain extreme (e.g., "no pain") to '10' representing the other pain extreme
|
2 weeks
|
|
Range of Motion at ankle joint
Time Frame: 2 weeks
|
Goniometer will be used to measure the pre and post treatment ranges of dorsiflexion and plantar flexion of ankle in supine and sitting positions.
|
2 weeks
|
|
Cadence (steps/min)
Time Frame: 2 weeks
|
Will asses gait parameters through 30 meters walk test.
steps counted x 60 / time (s)
|
2 weeks
|
|
Cycle time (s)
Time Frame: 2 weeks
|
Will asses gait parameters through 30 meters walk test.
time (s) x 2/steps counted
|
2 weeks
|
|
Gait speed
Time Frame: 2 weeks
|
Will asses gait parameters through 30 meters walk test.
Distance (m) /time (s)
|
2 weeks
|
|
Stride length(m)
Time Frame: 2 weeks
|
Will asses gait parameters through 30 meters walk test.
speed (m/s) x cycle time (s)
|
2 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- FUI/CTR/2024/23
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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