- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05050331
Comparative Effectiveness of Muscle Energy Technique and Trigger Point Release in Plantar Fasciitis
August 14, 2024 updated by: Dr Izza Ayub; PT, University of Faisalabad
Effectiveness of Muscle Energy Technique and Trigger Point Release in Plantar Fasciitis: A Comparative Study
Objective of this study was to compare the treatment effectiveness of MET and triggers point release in PF.
A single blinded, randomized clinical design was conducted.
Thirty patients was randomly allocated into two groups.
One group received muscle energy technique and the other receive trigger point release, while both groups performed self-stretching exercises as a home plan.
Their pain and foot function serve as outcome measure.
Treatment was given for 4 weeks, 3 sessions per week.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
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
-
-
Punjab
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Faisalābad, Punjab, Pakistan, 38000
- The University of Faisalabad
-
-
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
25 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Having unilateral plantar heel pain on weight-bearing
- Age 25-45
- Pain aggravated by walking few steps in the morning
- Having at least one identifiable trigger point in calf
Exclusion Criteria:
- Bilateral heel pain
- History of leg and foot tumor
- Lower limb fracture
- Lower limb injury,
- Achilles tendentious
- Ankle arthritis,
- Surgery or any vascular disease
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Muscle Energy Technique (MET) Group
Post-isometric relaxation was given as the form of MET.
It was applied to gastrocnemius and soleus muscle receiving a single set of 5 repetitions separately for 4 weeks, 3 sessions per week.
|
Muscle energy technique (MET) is an active manipulative technique that requires patient active muscle contraction of a respective muscle from a specific position in a specific direction with 10-20 percent force exerted by the patient which is resisted by the therapist in an attempt to relax and lengthen the muscle.
Self-stretching was performed 5 times twice a day with 20 seconds of intermittent stretch and 20 seconds relaxation time.
|
|
Experimental: Trigger Point Release Group
Trigger points of gastrocnemius muscle was released for 4 weeks, 3 sessions per week.
|
Self-stretching was performed 5 times twice a day with 20 seconds of intermittent stretch and 20 seconds relaxation time.
In trigger point release, a vertical downward pressure toward the trigger point for 90 seconds was applied with the therapist's thumb.
Three repetitions needed to be done with 30 seconds relaxation time.
After that, 3 longitudinal strokes in caudal to cranial direction are given by therapist's thumb over the taut band.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Foot Pain
Time Frame: Four Weeks
|
Numeric Pain Rating Scale was the primary outcome measure.
|
Four Weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Foot Function
Time Frame: Four Weeks
|
Foot function index was the secondary outcome measure of this study.
|
Four Weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Dr Sidra Majeed; PT, MSPP, The University of Faisalabad
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)
January 23, 2023
Primary Completion (Actual)
May 23, 2023
Study Completion (Actual)
May 24, 2023
Study Registration Dates
First Submitted
September 2, 2021
First Submitted That Met QC Criteria
September 14, 2021
First Posted (Actual)
September 20, 2021
Study Record Updates
Last Update Posted (Actual)
August 16, 2024
Last Update Submitted That Met QC Criteria
August 14, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TUF/DR/MSPP/174
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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