- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06109038
Effects of ITB Myofascial Release on Symptoms Associated With Knee OA.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Maria Khalid, MS-OMPT
- Phone Number: 0331-5369768
- Email: maria.khalid@riphah.edu.pk
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Pakistan General Hospital
-
Contact:
- Maria khalid, MS-0MPT
-
Contact:
- Nida Anwar, MS-OMPT*
-
Principal Investigator:
- NIDA ANWAR, MS-OMPT*
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- knee OA Grade 2 and Grade 3 according to kellgren and Lawrence grading scale
- Positive Ober's test
Exclusion Criteria:
- Patient with cardiovascular or medical illness.
- Patient with any severe trauma or surgery of knee.
- Knee deformity
- Low back pain with or without radiculopathy.
- Neurological illness
- Participants having any wound or scar on the site of treatment.
- Pregnant female
- Participants having co-morbidities such as neoplasm etc.
Study Plan
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: : Conventional PT + ITB release with graston technique
An emollient will be applied to the leg from the lateral joint line along the tibial condyle to just below the iliac crest. The instrument GT-4 will be used for treatment. The tool was used to assess the soft tissue in three locations on the lateral leg: anterior to the ITB, over the ITB, and posterior to the ITB. Brushing and strumming strokes were performed to the tissue utilising the instrument's convex surface. Treatment time with the instrument is 8 -10 mins . Conventional PT including Hot Pack for 5mins. Quadriceps setting exercises, short arc terminal knee extension, straight leg raise, ROM excercises, hamstring curls in prone lying position, quadriceps strengthening in high sitting position, gastrocnemius muscle stretching (10reps × 5sec × 2sets). Maitland mobilization (Grade 1, 2 and 3 for 10 repititions). |
An emollient will be applied to the leg from the lateral joint line along the tibial condyle to just below the iliac crest. The instrument GT-4 will be used for treatment. The tool was used to assess the soft tissue in three locations on the lateral leg: anterior to the ITB, over the ITB, and posterior to the ITB. Brushing and strumming strokes were performed to the tissue utilising the instrument's convex surface. Treatment time with the instrument is 8 -10 mins . Conventional PT including Hot Pack for 5mins. Quadriceps setting exercises, short arc terminal knee extension, straight leg raise, ROM exercises, hamstring curls in prone lying position, quadriceps strengthening in high sitting position, gastrocnemius muscle stretching (10reps × 5sec × 2sets). Maitland mobilization (Grade 1, 2 and 3 for 10 repetitions). |
Other: Conventional PT
Conventional PT including Hot Pack for 5mins.
Quadriceps setting exercises, short arc terminal knee extension, straight leg raise, ROM excercises, hamstring curls in prone lying position, quadriceps strengthening in high sitting position, gastrocnemius muscle stretching (10reps × 5sec × 2sets).
Maitland mobilization (Grade 1, 2 and 3 for 10 repititions).
|
Conventional PT including Hot Pack for 5mins.
Quadriceps setting exercises, short arc terminal knee extension, straight leg raise, ROM exercises, hamstring curls in prone lying position, quadriceps strengthening in high sitting position, gastrocnemius muscle stretching (10reps × 5sec × 2sets).
Maitland mobilization (Grade 1, 2 and 3 for 10 repetitions).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
WOMAC questionnaire
Time Frame: 4 WEEKS
|
The WOMAC is a reliable , valid, and responsive instrument for evaluating the severity of OA of the knee, with metric properties.
The WOMAC measures 5 items for pain (score range 0-20), 2 for stiffness (score range 0-8), and 17 for functional limitation (score range 0-68),
|
4 WEEKS
|
Numeric Pain Rating Scale
Time Frame: 4 WEEKS
|
The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain
|
4 WEEKS
|
Goniometer
Time Frame: 4 WEEKS
|
It is an instrument that measures the available range of motion at a joint.
|
4 WEEKS
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maria khalid, MS-OMPT, Riphah International University
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Nida Anwar / REC-01686
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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