- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05060042
Comparison of Whole Body Vibration With Bilateral Proprioceptive Training in Elderly
Comparison of Whole Body Vibration With Bilateral Proprioceptive Training in Elderly Population
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Elderly population is defined as 'people aged 65 or above'. Aging is a complex and challenging process of physiological changes and it is associated with decline of biological functions. Increasing age is linked with impairments in visual, proprioception, vestibular systems, decline in muscular strength and control of the lower limbs, balance/postural control, and of the mobility patterns which are known to be substantial hazards for fall, and these parameters have been found to be dynamically more disabled with getting older. Among all these factors, there is obvious decline in normal functioning and balance related issues, common in elderly population due to proprioceptive function loss that is the person is unable to sense his joint position and motion which ultimately results in mobility impairments.
Therefore, researchers have been looking for new approaches that are more feasible to improve the independence and physical mobility in older individuals and over the past decade the whole body vibrator (WBV) have been seeking attention for the beneficence of the elderly population. It is a neuromuscular training modality used to improve muscle strength, power, balance, mobility, cardiorespiratory rehabilitation, improves neuromuscular and musculoskeletal functions and general health both in healthy and as well as in orthopedic patients and neurologically diseased elderly population .Bilateral proprioceptive training is also used for impaired balance, proprioception loss and decreased ROM in elderly population. Proprioceptive receptors are present in our skin, muscles, tendons and joints with the help of which we can sense position and movement of limbs and trunk, sense of force and sense of heaviness in the absence of vision. The mechanoreceptors of the proprioception cause activation of central nervous system by initiating action potential through release of stored sodium in to the cells, this afferent sensory stimuli to the central nervous system is essential for the control of body movements
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Islamabad
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Rawalpindi, Islamabad, Pakistan, 46000
- Pakistan General Railway Hospital
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Rawalpindi, Islamabad, Pakistan, 46000
- Misbah Ghous
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants with balance and proprioception problems
- Those having BBS score between 21-54
- Intact cognition: MMSE >25
Exclusion Criteria:
- Subjects with recent trauma or any other neurodegenerative disorder.
- Subjects with cognitive and hearing impairments
- Subjects who cannot follow my command.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Whole body vibration group
WBV will be provided with a frequency of 6-26Hz with amplitude of 1-3mm 4-5 bouts(60 sec each) for 3 times a week.
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WBV will be provided with a frequency of 6-26Hz with amplitude of 1-3mm 4-5 bouts(60 sec each) for 3 times a week
|
|
Active Comparator: Bilateral proprioceptive training Group
Static balance training will be provided in first week for 3-4 times for 10 mints of single session. 3 times a week In 2nd and 3rd week dynamic balance training for 3 times with a session of 10 mints. In 4th week progressive balance training will be done with same frequency and duration. Tai chai exercises will be given for 20 mints 3 times a week |
Static balance training will be provided in first week for 3-4 times for 10 mints of single session. 3 times a week In 2nd and 3rd week dynamic balance training for 3 times with a session of 10 mints. In 4th week progressive balance training will be done with same frequency and duration. Tai chai exercises will be given for 20 mints 3 times a week |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time up and go test
Time Frame: Change from Baseline balance to 8th Weeks
|
The assessment of functional mobility in community dwelling elderly population, is assessed precisely by a balance test called time up and go test.Time taken to complete the task is actually indicating the level of functional mobility.
An elder participant taking less than 20 seconds to complete the task have been shown to be independent in ADLs.
Time taken more than 30 seconds by an older subject, indicates more dependent in ADLs and requires assistive devices for ambulation.
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Change from Baseline balance to 8th Weeks
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Performance-Oriented Mobility Assessment (POMA):
Time Frame: Change from Baseline balance and gait to 8th Weeks
|
• The Tinetti Performance Oriented Mobility Assessment (POMA) is a widely used clinical assessment tool that gives an insight into the abnormalities in balance and gait, and it has the ability to predict fall risk in elderly population.•
This scale has a total maximum score of 28 in which there is 12 score of gait assessment and 16 score of balance assessment.
The overall score of 25-28 indicates low fall risk, 19-24 represents moderate fall risk and <19 means there is high risk of fall in suspected elderly population.
This scale has been declared has a valid and reliable tool to assess balance and gait impairments
|
Change from Baseline balance and gait to 8th Weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Misbah ghous, MS, Riphah International University Islamabad
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Aneela Riaz
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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