Effects of Eccentric Exercises on Gait Parameters in Patellofemoral Pain Syndrome: A Quasi-Experimental Study

April 23, 2024 updated by: Foundation University Islamabad
This study is a quasi experimental and the purpose of this study is to determine the effects of eccentric exercises on gait parameters in patellofemoral pain syndrome: a quasi - experimental study

Study Overview

Detailed Description

The purpose of this study is to determine the effects of eccentric exercises on gait parameters in patellofemoral syndrome : a - quasi experimental study

Pain , gait parameters, ROM and dynamic knee valgus angle of young adults (age : 18-35 years ) will be determined using:

  1. Numeric pain rating scale
  2. Goniometer
  3. 30 meter walk test
  4. dynamic knee valgus angle via quentic software Data will be before and after the intervention protocol for each participant. Data collection procedure: Participants of interest would be approached and explained about the research. Informed written consent will be taken. Pre and post intervention scores will be recorded.

Study Type

Interventional

Enrollment (Estimated)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Recruiting
        • Foundation University College of Physical Therapy
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age 18-35 years
  • Females
  • Having pain from at least 2 months
  • Pain score greater than 3 on NPRS
  • Retro patellar pain in at least two of the following activities:

    1. Ascending, descending stairs
    2. Hooping / jumping
    3. Prolonged sitting with flexed knees
    4. Kneeling and squatting
  • Pain on palpation of medial or lateral patellar facet.
  • Pain on palpation on anterior portion of medial or lateral femoral condyles.

Exclusion Criteria:

  • Diagnosed with Chondromalacia patellae
  • Instability of tibiofemoral joint
  • Subluxation of patellofemoral joint
  • Patellar instability
  • Previous surgery of lower limb
  • Negative findings on examination of knee ligaments, menisci and bursa.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Interventional group
There will be only one group in the study. After application of Mc Connell taping, patients will perform eccentric exercises taught by the therapist for 6 weeks. Mentioned below are detailed protocols for the treatment of patellofemoral pain syndrome.
Begin with the patient in supine lying with the knee slightly bent. The knee should be completely relaxed and a foam roller or rolled up towel under the knee. Start the tape in line with the middle of the knee cap at the outer aspect of the knee. Using your thumb on top of the sports tape, gently push the patella towards the inner aspect of the knee whilst simultaneously using your fingers to pull the skin at the inner aspect of the knee towards the patella. Finish this taping technique at the inner aspect of the knee ensuring you have created some wrinkling of the skin at the inner aspect of the knee.

Performed for 6 weeks, in 3 sets of 10-12 repetitions each day. Detailed protocol is as under:

Warm up phase (5 minutes) It will comprise of following components 5 minutes warm up exercise protocol: Marching in place while swinging your arm, rotating toe touching, walking jacks, leg swings, arm circles, shoulder shrugs Eccentric exercises: Each of the following exercise will be performed for 30 seconds, repetitions and hold time will increase with increasing weeks according to patient's stamina.

Straight leg raise, side lying hip abduction, single leg bridging, supported double leg squatting, hip hikes,supported single leg squatting Following is the detailed description of Cool down phase: Hip stretch, cat cow stretch, oblique stretch, lower back stretch, calf stretch, cross body shoulder stretch

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dynamic knee valgus angle
Time Frame: 6 weeks
2D analysis using a video camera will be used to analyze dynamic knee valgus, specifically the inward movement of the knees during task performance. Participants will be instructed to perform a single-leg squat task. They will also be directed to adequately flex the contralateral knee to prevent the foot from touching the floor. A digital video camera positioned at a 90-degree angle to the frontal plane will be placed on a tripod stand 2m in front of the participant's landing point at knee level for 2D video recording purposes. The recorded video will be processed into slow motion and exported to Quintic® biomechanics v31 software.. Dynamic knee valgus angle (DKVA) will be calculated at the intersection point of two lines: the first line connecting markers placed on the anterior superior iliac spine (ASIS) and the middle of the tibio femoral joint, and the second line connecting the middle of the tibio femoral joint and the middle of the ankle mortise.
6 weeks
Hip Range of Motion
Time Frame: 6 weeks
It will be measured with goniometer
6 weeks
Knee Range of Motion
Time Frame: 6 weeks
It will be measured with goniometer
6 weeks
Pain intensity
Time Frame: 6 weeks
Numeric pain rating scale will be used to access pain of the subject pre and post intervention.
6 weeks
Gait Speed
Time Frame: 6 weeks
Gait speed is the distance that the patient has covered per unit time Calculated as: Gait speed = Distance (m) x time (s)
6 weeks
Cadence
Time Frame: 6 weeks
Cadence is the number of steps patient takes per unit time. Calculated as: Cadence (steps/min) = steps counted x 60 / time (s)
6 weeks
Stride length
Time Frame: 6 weeks
Stride length is the distance between two heel strikes of the same foot. Calculated as: SL (m) = speed (m/s) x cycle time (s)
6 weeks
Step length
Time Frame: 6 weeks
Step length is the vertical distance between heels of two feet. Calculated as: Step length (m) = stride length/2
6 weeks
Cycle length
Time Frame: 6 weeks
Cycle length is the time between the two heel strikes of one foot. Calculated as: Cycle time (s) = time (s) x 2/steps counted
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 15, 2023

Primary Completion (Estimated)

November 20, 2024

Study Completion (Estimated)

November 20, 2024

Study Registration Dates

First Submitted

April 23, 2024

First Submitted That Met QC Criteria

April 23, 2024

First Posted (Actual)

April 29, 2024

Study Record Updates

Last Update Posted (Actual)

April 29, 2024

Last Update Submitted That Met QC Criteria

April 23, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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