- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05424341
Effects Of Muscle Energy Versus Counter Strain Technique on Pain, Function and Satisfaction Level in Planter Fasciitis
Comparative Effects Of Muscle Energy Technique And Counter Strain Technique On Pain, Functional Status And Satisfaction Level In Planter Fasciitis Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Heel pain is one of the most prevalent musculoskeletal diseases of the lower limb, affecting both physically active and sedentary people. Amongst the possible causes, planter fasciitis is one of the most common cause of heel pain.
Planter fasciitis is a degenerative syndrome resulting from the repeated injury at its origin on the calcaneus. Its most common symptom is discomfort in the plantar area of the foot and, more specifically, in the inferior part of the heel. It is frequently more intense while taking your first steps in the morning or after a period of physical inactivity, and it worsens with prolonged standing or weight-lifting activities. It is not frequently linked to nocturnal discomfort or paresthesia.
Different physiotherapy treatment conventions help in pain relieving for example, rest, taping, stretching, orthosis-night brace, Silicon heel cups and myofascial release. This study will compare the effects of Muscle Energy Technique versus Counterstrain Technique in patients with plantar Fasciitis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
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Lahore, Punjab, Pakistan, 54000
- The University of Lahore
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Age 20 to 68 years.
- Both male and female.
- Patients are clinical diagnosed by the orthopedic surgeon.
- Patients present with pain that persist for more than 4 weeks in heel and planter surface of foot.
- Pain with the first steps after inactivity
Exclusion Criteria:
• Patients with history of ankle and foot fracture.
- Congenital or acquired deformity of ankle and foot.
- Patients with arthritis.
- Pervious history of surgery for planter fasciitis.
- Patients use an assistive device for walking.
- Patients use corticosteroid injection in heel.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A
This group will receive muscle energy technique along with routine physical therapy.
This protocol will be given for 3 alternative days for 2 weeks .
Each session will be of 50 mins.
Data will be collected at baseline , at 1st week and at 2nd week.
|
For Gastrocnemius muscle, subject will be in supine position keeping knee fully extended and therapist on affected side in walking position.
The subject's ankle joint will be dorsiflexed until a resistance feel and will ask to hold this position and exert 20% of force towards plantar flexion for a period of 5 to 7 seconds.
Resistance will be released and relaxation of 5 seconds will be given during which the ankle will was passively dorsiflexed to a new barrier.
5 repetitions will be given.
|
|
Active Comparator: Group B
This group will receive counterstrain technique along with routine physical therapy.
This protocol will be given for 3 alternative days for 2 weeks .
Each session will be of 50 mins.
Data will be collected at baseline , at 1st week and at 2nd week.
|
Therapist places thumb on tender point at plantar fascia insertion while patient in supine position with ipsilateral knee flexed.
Plantar flex the toes and ankle while monitoring sore site with thumb, curling around tender point until monitoring thumb feels symptomatic relief.
Supination/pronation of foot will be added if necessary.
The position of ease will be maintained for 90 secs until tissues beneath monitoring thumb softens.
Tender spot is re-evaluated once the foot is returned to neutral without moving the thumb.
It will be repeated 3 times for 30 secs resting interval in-between
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: Change in pain intensity will be measured at baseline, at end of first week, at end of second week
|
Pain intensity will be measured by Visual Analogue Scale (VAS)
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Change in pain intensity will be measured at baseline, at end of first week, at end of second week
|
|
Function
Time Frame: Change in Functional Status will be measured at baseline, at end of first week, at end of second week
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Functional status will be measured by Foot and Ankle Ability Measure (FAAM)
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Change in Functional Status will be measured at baseline, at end of first week, at end of second week
|
|
Satisfaction Level
Time Frame: Level of satisfaction will be observed at end of First Session, at end of first week, at end of second week
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Satisfaction level will be measured by Short-Form Patient Satisfaction Questionnaire (PSQ-18)
|
Level of satisfaction will be observed at end of First Session, at end of first week, at end of second week
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Ayesha Jamil, M.Phil, The University of Lahore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- Taliah Bashir Sindhu
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
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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