search
Back to results

Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome

Primary Purpose

Patellofemoral Pain Syndrome

Status
Recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
whole body vibration
traditional exercise group
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Patellofemoral Pain Syndrome focused on measuring Patellofemoral pain syndrome, vibration, Planter/Dorsi ratio, pain

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age: Adults aged 18 -35 years Symptoms: Pain in the anterior or retro patellar knee region during activities such as running, jumping, squatting, or prolonged sitting Duration: Pain lasting at least 6 weeks Exclusion Criteria: Presence of other knee conditions: Individuals with PFPS who also have other knee conditions such as ligament or meniscal injuries, osteoarthritis, or patellar tendinopathy may be excluded. History of knee surgery: Patients who have undergone any knee surgery may be excluded as this may affect the outcomes of the study. Systemic conditions: Patients with systemic conditions that may affect the musculoskeletal system such as rheumatoid arthritis or lupus may be excluded. Pregnancy: Pregnant women with PFPS may be excluded as pregnancy may affect the outcomes of the study. Inability to comply with study requirements: Patients who are unable to comply with the study requirements such as attending follow-up appointments or completing questionnaires may be excluded.

Sites / Locations

  • Faculty of physical therapy , cairo universityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

whole body viberation group

control group

Arm Description

Outcomes

Primary Outcome Measures

Dorsi/planter torque ratio
dorsi/planter torque ratio will be measured through the Biodex System 4-Pro Isokinetic Strength Dynamometer for assessment of muscle torque
functional activities
Kujala Anterior Knee Pain Scale, which includes questions related to functional activities.
Pain intensity
10 cm Visual Analogue Scale (VAS) was used to assess pain intensity during activity in patients with patellofemoral pain (PFP). The scale ranged from 0, indicating "no pain," to 100, representing the "worst pain imaginable.

Secondary Outcome Measures

Full Information

First Posted
August 19, 2023
Last Updated
August 28, 2023
Sponsor
Cairo University
search

1. Study Identification

Unique Protocol Identification Number
NCT06017778
Brief Title
Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome
Official Title
Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome: Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 30, 2023 (Anticipated)
Primary Completion Date
October 30, 2023 (Anticipated)
Study Completion Date
November 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patellofemoral pain syndrome (PFPS) can significantly affect an individual's ability perform to functional activities, such as walking, running, climbing stairs, and sitting for prolonged periods. PFPS is often associated with pain and discomfort in the front of the knee, which can limit an individual's range of motion and cause difficulty with weight-bearing activities. The pain may also be exacerbated by activities that involve bending the knee, such as squatting or kneeling. Whole body vibration (WBV) has been suggested as a potential intervention for patellofemoral pain syndrome (PFPS). Some studies have shown that WBV can improve muscle strength, balance, and proprioception, which are all factors that may contribute to PFPS. Additionally, WBV may help reduce pain and improve functional abilities in individuals with PFPS However, the evidence for the effectiveness of WBV as an intervention for PFPS is still limited, and more research is needed to fully understand its potential benefits and limitations. It is important to note that WBV may not be suitable for all individuals with PFPS.
Detailed Description
Patellofemoral pain syndrome (PFPS) can significantly affect an individual's ability perform to functional activities, such as walking, running, climbing stairs, and sitting for prolonged periods. PFPS is often associated with pain and discomfort in the front of the knee, which can limit an individual's range of motion and cause difficulty with weight-bearing activities. The pain may also be exacerbated by activities that involve bending the knee, such as squatting or kneeling. Whole body vibration (WBV) has been suggested as a potential intervention for patellofemoral pain syndrome (PFPS). Some studies have shown that WBV can improve muscle strength, balance, and proprioception, which are all factors that may contribute to PFPS. Additionally, WBV may help reduce pain and improve functional abilities in individuals with PFPS. However, the evidence for the effectiveness of WBV as an intervention for PFPS is still limited, and more research is needed to fully understand its potential benefits and limitations. It is important to note that WBV may not be suitable for all individuals with PFPS. HYPOTHESES: There will be no significant difference on dorsi/planter flexor ratio , functional activities and pain level after adding the whole body vibration to traditional treatment of PFPS RESEARCH QUESTION: What is the impact of whole-body vibration on dorsi/planter flexor ratio, functional activities and pain levels in individuals with PFPS?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patellofemoral Pain Syndrome
Keywords
Patellofemoral pain syndrome, vibration, Planter/Dorsi ratio, pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
whole body viberation group
Arm Type
Experimental
Arm Title
control group
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
whole body vibration
Intervention Description
patients will receive WBV training in addition to traditional training will be performed on a tri-planar (mostly vertical, Z axis) oscillating vibration platform (Power PlateR pro5™; Power Plate North America, Inc., Northbrook, IL,USA) for 20-30 minutes per session. WBV training will be supervised and performed in a clinic three days a week with at least one day between each session for four weeks (total of 12 sessions).
Intervention Type
Other
Intervention Name(s)
traditional exercise group
Intervention Description
10 minutes warm-up (lower extremity stretching exercises), 20-30 minutes period of strength exercises with three sets of 10-15 repetitions (isometric quadriceps setting, knee extensions, double-legged wall squat), and 5 minutes cool-down (lower extremity stretching exercises). Lower extremity stretching exercises consisted of quadriceps, hamstring, gastrocnemius and iliotibial band stretching with 3 repetitions for 30 s each muscle.
Primary Outcome Measure Information:
Title
Dorsi/planter torque ratio
Description
dorsi/planter torque ratio will be measured through the Biodex System 4-Pro Isokinetic Strength Dynamometer for assessment of muscle torque
Time Frame
one month
Title
functional activities
Description
Kujala Anterior Knee Pain Scale, which includes questions related to functional activities.
Time Frame
one month
Title
Pain intensity
Description
10 cm Visual Analogue Scale (VAS) was used to assess pain intensity during activity in patients with patellofemoral pain (PFP). The scale ranged from 0, indicating "no pain," to 100, representing the "worst pain imaginable.
Time Frame
one month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: Adults aged 18 -35 years Symptoms: Pain in the anterior or retro patellar knee region during activities such as running, jumping, squatting, or prolonged sitting Duration: Pain lasting at least 6 weeks Exclusion Criteria: Presence of other knee conditions: Individuals with PFPS who also have other knee conditions such as ligament or meniscal injuries, osteoarthritis, or patellar tendinopathy may be excluded. History of knee surgery: Patients who have undergone any knee surgery may be excluded as this may affect the outcomes of the study. Systemic conditions: Patients with systemic conditions that may affect the musculoskeletal system such as rheumatoid arthritis or lupus may be excluded. Pregnancy: Pregnant women with PFPS may be excluded as pregnancy may affect the outcomes of the study. Inability to comply with study requirements: Patients who are unable to comply with the study requirements such as attending follow-up appointments or completing questionnaires may be excluded.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Radwa Elshorbagy
Phone
00966500920691
Email
Rtelshorbagy@ju.edu.sa
Facility Information:
Facility Name
Faculty of physical therapy , cairo university
City
Giza
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Radwa

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
6 months after publication
IPD Sharing Access Criteria
study protocol

Learn more about this trial

Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome

We'll reach out to this number within 24 hrs