- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05058235
Comparison of Active Release Technique and Bent Leg Raise In Osteoarthritis.
Comparison Of Effects Of Active Release Technique And Bent Leg Raise On Hamstring Flexibility In Patients With Knee Osteoarthritis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Federal
-
Islamabad, Federal, Pakistan, 44000
- Noor Physio and Sports Injury Clinic, G-8 Markaz
-
-
Punjab
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Rawalpindi, Punjab, Pakistan, 46000
- Riphah Rehabilitation Center, Westridge campus, Potohar Tower, Peshawar Road
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosed patients of Knee Osteoarthritis
- Hamstring length less than 160 degrees
- Minimum history of 3 months
- Willing to participate
Exclusion Criteria:
- Patients who have passive knee extension more than 160 degrees
- Patients with less than 3 months history
- Patients who have osteoarthritis of other than the knee joint
- Patients with history of fracture
- Patients with post surgical history
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 |
|---|---|
|
Experimental: Active Release Technique
Hot pack, TENS, Quadriceps Isometric strengthening, Active Release Technique
|
Moist Hot pack 10 mins/1 set/ (6 days/ week), TENS 20 mins/1 set/ (6 days/ week), Quadriceps Isometric Strengthening 5 sec hold, 10 reps/ 1 set/(6 days/ week), Active release Technique 5 reps/ 1 set/ (6 days/ week) A total of 2 weeks (12 sessions, 6 sessions/ week) were given each consisting of 40 mins. |
|
Active Comparator: Bent leg raise
Hot pack, TENS, Quadriceps Isometric strengthening, Bent leg raise
|
Moist Hot pack 10 mins/1 set/ (6 days/ week), TENS 20 mins/1 set/ (6 days/ week), Quadriceps Isometric Strengthening 5 sec hold, 10 reps/ 1 set/(6 days/ week), Bent leg raise 5 sec hold/ 5 sec stretch/ 3 reps/ 1 min rest interval/ 1 set/ (6 days/ week). A total of 2 weeks (12 sessions, 6 sessions/ week) were given each consisting of 40 mins. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hamstring flexibility
Time Frame: 12 days
|
Changes from baseline, Hamstring flexibility was measured through passive knee extension test with the help of Goniometer.
Normal value of knee extension angle is 180 degrees.
Values decreased than 160 degree represents hamstring tightness.
|
12 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional outcome
Time Frame: 12 days
|
Changes from baseline, Functional outcome was taken through western Ontario McMaster Universities Osteoarthritis Index tool.
It comprises three sections containing 24 items.
Score ranges from 0 to 96. 0 representing a healthy state and higher scores indicating worst health.
|
12 days
|
|
Pain on Visual analogue Scale
Time Frame: 12 days
|
Changes from baseline, Pain was measured through Visual Analogue Scale.
It comprises of a continuous scale of 10cm line.
0 to 4mm represents "no pain", 5mm to 44mm indicates "mild pain", whereas 45mm to 74mm indicates "moderate pain" and continues to the range of "worst pain" between 75mm to 100 mm.
|
12 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Asghar Khan, PhD, 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 (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
- REC/00853 Syeda Nayab Sheeraz
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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