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Completed

NCT Number: NCT04496622

WBV Training on Physical Function and Muscle Strength in Knee OA

In this study compare different frequencies of whole body vibration training on physical function and muscle strength in patients with knee osteoarthritis.

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Key information

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Railway General Hospital

Rawalpindi, Punjab Province, 44000, Pakistan

About this study

This randomized controlled trial is to compare different frequencies of whole-body vibration (WBV) training on physical function and quadriceps muscle strength in patients with knee osteoarthritis and further will be researched which frequencies are effective for knee OA patients and how much WBV training is useful modality for knee osteoarthritic patients. This research will have significant effects in improving muscle strength and functional level of knee OA patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 40-70 years
  • Both genders
  • Kellgren and Lawrance grade 2 and 3.
  • Pain symptoms for at least 3 months
  • Had no previous experience in WBV

Exclusion criteria

  • Knee surgery in the past 6 months
  • Patient with acute symptomatic knee OA
  • Unable to walk unaided
  • Diagnosed with other muscular and joint disease that affect the lower limb function
  • Patient with any neurological conditions
  • History of trauma to knee joint during last week.

Treatment and study plan

WBV technique

Other

Whole body vibration with frequency of 16-25 Hz were given from week 1-8 for 10 minutes/10 repetitions. Time were increased weekly Convention therapy were hot pack 10 minutes, stretching exercise (SLR) 10 repetition x 3 sets and quadriceps exercise 10 repetition x 3 sets.

3 session/week for 8 weeks

Whole body vibration technique

Other

Whole body vibration with frequency of 26-35 Hz were given from week 1-8 for 10 minutes/10 repetitions. Time were increased weekly Convention therapy were hot pack 10 minutes, stretching exercise (SLR) 10 repetition x 3 sets and quadriceps exercise 10 repetition x 3 sets.

3 session/week for 8 weeks

Primary outcomes

  1. Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

    Time frame: 8 week

    Changes from base line WOMAC is a widely used self-administered health status measure used in assessing pain, stiffness, and function in patients with OA of hip and knee. It consists of 3 sections with the total score of 96

  2. 1 Repetition maximum (1 RM)

    Time frame: 8 week

    Changes from base line 1 RM measure muscle strength with maximum amount of weight that a person can possibly lift for one repetition

Secondary outcomes

  1. Visual Analog Scale (VAS)

    Time frame: 8 week

    Changes from baseline visual analog scale for pain starting from 0-10

  2. Timed up and Go test (TUG)

    Time frame: 8 week

    Changes from baseline time up and go test to determine fall risk and measure the progress of balance, sit to stand and walking.

  3. 6 minute walk test

    Time frame: 8 week

    Changes from baseline 6 minute walk test measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Comparison of Different Frequencies of Whole Body Vibration Training on Physical Function and Muscle Strength in Patients With Knee Osteoarthritis

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Aug 3, 2020
Registry last updated
Aug 3, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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