- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05110326
Ergon Technique Versus PNF Stretching on Hamstring Flexibility in Knee Osteoarthritis
March 15, 2023 updated by: Riphah International University
Comparison of Ergon Technique Versus Proprioceptive Neuromuscular Facilitation Stretching on Hamstring Flexibility in Patients With Knee Osteoarthritis
The study will be a randomized control trial and will be conducted in Pakistan Railway Hospital Rawalpindi.
A sample of 60 participants will be taken.
Patients will be divided into two groups (A&B) of 30 participants in each group by sealed envelope method.
Hot pack will be applied to both groups for 15 minutes at the start of intervention.
ERGON Technique(IASTM) will be applied to group A along with strengthening exercise.
Proprioceptive Neuromuscular Facilitation (PNF) stretching will be given to group B along with strengthening exercise.
A 35 minute session will be given to the patients and 3 sessions will be given once a week.
Intervention will be given for 6 weeks.
The outcome measure will be Visual analog Scale (VAS), Western Ontario and McMaster Universities Arthritis Index (WOMAC), and Active Knee Extension Test (AKE) will be measured at baseline and at the end of 6th week.
Data will be analyzed by SPSS 22.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
57
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
-
-
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Islamabad, Pakistan, 44000
- RHS Rehabilitation Centre
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-
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
35 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Unilateral/bilateral osteoarthritis
- Participants with unilateral/bilateral hamstring tightness
- 200 from Active Knee Extension test
- Grade 1 and 2 in Kellgren and Lawrence criteria for knee osteoarthritis
Exclusion Criteria:
- Participant failing to fall in the category below will be excluded from the study:
- Any lower extremity injury in past 3 months
- Any fracture or surgery done for pelvis, hip or knee.
- Any neurological symptoms.
- Any recent knee reconstructive surgery
- Burns of lower extremities
- Other musculoskeletal disorders associated with knee joint, Iliotibial band, adductor muscle and Sartorius muscle tightness
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ERGON Technique Group
Patients in this group will receive ERGON Technique along with conventional therapy
|
|
|
Experimental: Proprioceptive Neuromuscular Facilitation(PNF) stretching Group
Patients in this group will receive Proprioceptive Neuromuscular Facilitation (PNF) stretching along with conventional therapy
|
Strengthening Exercises:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analog Scale (VAS)
Time Frame: 6 Weeks
|
The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain.
Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain.
It is used to find out the intensity of pain.
|
6 Weeks
|
|
Western Ontario and McMaster Universities Arthritis Index(WOMAC)
Time Frame: 6 Weeks
|
The Western Ontario and McMaster Universities Arthritis Index(WOMAC) is widely used in the evaluation of Hip and Knee Osteoarthritis.
It is a self-administered questionnaire consisting of 24 items divided into 3 subscales.
|
6 Weeks
|
|
Active Knee Extension Test
Time Frame: 6 Weeks
|
The Active Knee Extension Test is used to assess hamstring muscle length and the range of active knee extension in the position of hip flexion.
|
6 Weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 10, 2022
Primary Completion (Actual)
May 30, 2022
Study Completion (Actual)
June 25, 2022
Study Registration Dates
First Submitted
October 26, 2021
First Submitted That Met QC Criteria
October 26, 2021
First Posted (Actual)
November 5, 2021
Study Record Updates
Last Update Posted (Actual)
March 17, 2023
Last Update Submitted That Met QC Criteria
March 15, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Narmeen Anjum
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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