Effects of Virtual Reality Rehabilitation and Muscle Energy Technique in Patients With Patellofemoral Pain Syndrome.

Sponsor
Riphah International University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05971966
Collaborator
(none)
32
1
2
8
4

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Virtual Reality technique
  • Other: Muscle energy technique
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effect of Virtual Reality Rehabilitation and Muscle Energy Technique in Patients With Patellofemoral Pain Syndrome.
Anticipated Study Start Date :
Aug 28, 2023
Anticipated Primary Completion Date :
Mar 28, 2024
Anticipated Study Completion Date :
Apr 28, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Virtual Reality technique

Virtual reality technique+ Conventional PT

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

Experimental: Muscle energy technique

Muscle energy technique + Conventional PT

Other: 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

Outcome Measures

Primary Outcome Measures

  1. Kujala questionnaire [4 weeks]

    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.

Secondary Outcome Measures

  1. Visual analogue scale (VAS) [4 weeks]

    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

  2. Goniometer [4 weeks]

    It is an instrument that measures the available range of motion at a joint.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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,

  1. 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dr.z pain & brain physiotherapy center Islamabad Punjab Pakistan

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: KINZA ANWAR, MS-OMPT, RIPHAH INTERNATIONAL UNIVERSITY,ISLAMABAD,PAKISTAN

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT05971966
Other Study ID Numbers:
  • REC/Nayab Mehmood
First Posted:
Aug 2, 2023
Last Update Posted:
Aug 2, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2023