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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05971966
Other study ID # REC/01652 Nayab Mehmood
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 30, 2023
Est. completion date April 28, 2024

Study information

Verified date August 2023
Source Riphah International University
Contact Kinza Anwar, MS-OMPT
Phone +92-3239735427
Email kinza.anwar@riphah.edu.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this randomized controlled trial is to determine the effects of Virtual reality rehabilitation and muscle energy techniques in patients with patellofemoral pain syndrome for reducing pain, enhancing knee range of motion and improve functional activities.


Description:

Muscle energy technique is defined as a manual treatment in which patient produces a contraction in a precisely controlled position and direction against the counterforce applied by a manual therapist. Applications of MET to stretch and increase myofascial tissue extensibility seem to affect viscoelastic and plastic tissue property. Virtual reality generates a virtual world in three dimensional space through a computer simulation that stimulates user senses, such as sight and hearing, making users feel as if they are immersed in it. VRBR is effective in improving knee pain, ROM, strength and functions. immersive VR is more appropriate for pain reduction, improving range of motion and functional activities. It distracts the patient and allows to perform active and rehabilitation exercises to reduce cognitive attention in pain and avoidance behavior.


Recruitment information / eligibility

Status Recruiting
Enrollment 32
Est. completion date April 28, 2024
Est. primary completion date March 28, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Age group 18-40 - Both males and females - Retropatellar or anterior knee pain for atleast past 3 months - Having knee pain in atleast 2 activities among stair ascent and descent,squatting over 90 degrees, running,jumping,kneeling and prolong sitting with knees flexed. - Experience pain in one of the following knee tests; a) pain on patellar grinding test, b) pain on apprehension test, c) pain during resisted extension of the knee during 90 degree flexion Exclusion Criteria: - Cervical radiculopathy - Neurological disorder - Pregnancy - Rheumatoid arthritis - Hip or ankle injuries - Patellar instabilities - Meniscal or ligament tear - Who have visual or auditory problems - With cognitive issues - Previous surgery related to lower limbs/ radiculopathy - having received knee injections of corticosteroids or hyaluronic acid - knee osteoarthritis - drug use that affects the balance during the past 72 h.

Study Design


Intervention

Other:
Virtual Reality technique
They would be receiving treatment as follow: Specific exercises by using virtual reality with conventional treatment. The VR game included holopoint,hot squat and portal stories that will target the hamstring, quadriceps and gluteas muscles.Frequency: 3 times/week for 4 weeks Intensity: moderate intensity (pain free) Time: 20 mins Type: virtual reality gaming exercises Conventional PT including patellar mobilization+ ultrasound on anterior knee in supine lying + stretching of ITB . Frequency: 10 reps with 5 sec hold for 3 times/week for 4 weeks Intensity: moderate-high intensity (depending on pain tolerance) Time: 10 mins
Muscle energy technique
They would be receiving treatment as follow: Muscle energy technique of quadriceps and hamstring muscles. Frequency: 3 times/week for 4 weeks Intensity: moderate intensity (pain free) Time: 20 mins Type: Muscle energy technique to improve range of motion. Conventional PT including patellar mobilization + ultrasound on anterior knee in supine lying + stretching of ITB. Frequency: 10 reps with 5 sec hold for 3 times/week for 2 weeks Intensity: moderate-high intensity (depending on pain tolerance) Time: 10 mins

Locations

Country Name City State
Pakistan Dr.z pain & brain physiotherapy center Islamabad Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Kujala questionnaire It is a self administered questionnaire for patients with PFPS that consists of 13 questions that relate to specified activities, pain severity, and clinical symptoms. The scores range from a maximum of 100 to a minimum of 0, with lower scores indicating greater pain and disability. 4 weeks
Secondary Visual analogue scale (VAS) VAS is a qualitative pain measurement tool that assigns integer numbers between zero and 10 to different pain levels, where zero means no pain and 10 means excruciating pain. VAS is a reliable scale to measure knee pain 4 weeks
Secondary Goniometer It is an instrument that measures the available range of motion at a joint. 4 weeks
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