- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06130774
Effects of Retro-walking in Patients With Knee OA
Effects of Retro-walking in Knee OA Along With Conventional Therapy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Knee pain is a major symptom of knee osteoarthritis (OA) that lead to stiffness, and capsular contracture along with muscle spasm. Decreased flexibility of muscles reduces the joint range of motion and thus contributes to increase in the stiffness of the joint lead to physical disability in persons with knee OA.Eighty percent of persons with knee OA experience pain and 25% struggle to perform activities of daily living.) Retro-walking is sometimes referred to as backward walking, has been thought to be used already for several decades in China, Japan and Europe to get a physical workout, improve sport performance, promote balance and also to stay mentally fit .
In fact in Europe, they have races which vary from sprints to the 26.2 miles marathon.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Rawalpindi, Punjab, Pakistan, 46000
- Riphah international hospital Sihala
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Unilateral Knee OA .
- Kellgren-Lawrence grading (grade 1 and 2)
- Participants fulfilling three out of the six clinical criteria listed by the American College of Rheumatology The criteria are Age >40 years, Morning stiffness lasting <30 mins. Crepitus with active motion, Bony tenderness, Bony enlargement and No warmth to touch and diagnosed to have knee OA
- Pain more than 6 weeks
Exclusion Criteria:
- Trauma or surgery in the last 6 months.
- Hip, knee, and foot deformities.
- Stroke and other neurovascular issues.
- Severe pain (greater than 7 in NPRS)
- Difficulty in walking for 10 min continuously.
- Obesity (body mass index greater than 25 kg/m2 )
- Osteoporosis
- Patients having any systemic joint pathology, inflammatory joint disease (e.g. rheumatoid arthritis, gouty arthritis, psoriatic arthritis).
- Patients who had any neurological deficit, myelopathy any mental illness.
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: Retro walking and conventional
Patient will start retro walking with first he/she will raise his/her one foot with toe off first then heel will be off from ground.
swing phase of same leg would be done in backward direction with flexion on knee and extension will be performed on hip.
Then patient will place the same foot on ground behind the other foot, with toe touch first on ground, and so this way patient would continue for 20 minutes continue his retro-walk for 20 minutes.
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Patient will start retro walking with first he/she will raise his/her one foot with toe off first then heel will be off from ground.
swing phase of same leg would be done in backward direction with flexion on knee and extension will be performed on hip.
Then patient will place the same foot on ground behind the other foot, with toe touch first on ground, and so this way patient would continue his retro-walk for 20 minutes
|
|
Active Comparator: conventional therapy
Hot pack in supine lying (10min) TENS (10min ) Tibiofemoral mobilization (grade 1,2 ,3) (10rep) Static quadriceps exercise in supine (10rep x 3sec x2set) hip abduction in side lying(10repx 2set) knee bending exercise in prone lying ( 10rep x 2set) Hamstring stretch in supine ( 10 rep x 2 set)
|
Hot pack in supine lying (10min) TENS (10min ) Tibiofemoral mobilization (grade 1,2 ,3) (10rep) Static quadriceps exercise in supine (10rep x 3sec x2set) hip abduction in side lying(10repx 2set) knee bending exercise in prone lying ( 10rep x 2set) Hamstring stretch in supine ( 10 rep x 2 set)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NPRS
Time Frame: six 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.
NPRS exhibited moderate reliability
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six weeks
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WOMAC
Time Frame: six weeks
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The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) is a widely used, proprietary set of standardized questionnaires used by health professionals to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain, stiffness, and physical functioning of the joints.
Higher scores indicate worse pain, stiffness, and functional limitations.
The WOMAC measures five items for pain (score range 0-20), two for stiffness (score range 0-8), and 17 for functional limitation (score range 0-68),
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six weeks
|
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Calcon Calculator
Time Frame: six weeks
|
To calculate your walking stride length, divide the number of steps you took by two and divide that number into the measured distance.
If it took you 18 steps to cover 21 feet, divide the number of steps (18) by 2 to get the number of strides.
Then take the answer (9) and divide it into the distance.
Distance in feet/number of strides = stride length.
In this case, you took nine strides in 22 feet, so your stride length would be 2.4 feet.
For step length divide the number of steps into the measured distance.
Distance in feet/number of steps = step length.
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six weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maria khalid, MSOMPT, 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
- REC 01681 MAIRA KANWAL
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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