- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07002736
- Original Trial
Impact of Balance Training in Community-Dwelling Older Adults After Recovery From COVID-19
The Impact of Balance Training on Functional Performance and Fall Risk in Community-Dwelling Older Adults Following Recovery From COVID-19"
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Older adults recovering from COVID-19 frequently face persistent physical limitations due to the virus's impact on the respiratory, muscular, and neurological systems. These limitations often manifest as impaired balance, reduced functional mobility, and increased risk of falls-conditions further exacerbated by prolonged inactivity or hospitalization during illness.
This research focuses on evaluating the effectiveness of a structured balance training program using The Biodex Stability System in older adults living independently in the community after recovering from COVID-19.
Participants are assessed using validated tools such as the Berg Balance Scale, Timed Up and Go (TUG) test, and The Biodex Stability System to measure changes in balance performance, fall risk, and confidence in daily movement.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Jeddah, Saudi Arabia, 32143
- BMC
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- were being older adults (aged ≥60 years), recovered from infection during the last 6 month,
Exclusion Criteria:
- Individuals were excluded if they have medical history of musculoskeletal trauma or surgery, systemic disease that could affect standing or walking, visual, auditory, or cognitive impairment that preclude the ability to comprehend the instructions during conduction of the study protocol.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The Biodex training
Balance Training
|
Participants will undergo balance training using the Biodex Balance System plus Traditional balance training
Traditional balance training only
|
|
Active Comparator: Control
Traditional Balance Training
|
Traditional balance training only
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Biodex Balance indices
Time Frame: Pre and Post 12 weeks
|
The Biodex Stability System will be used to evaluate dynamic postural stability
|
Pre and Post 12 weeks
|
|
Berg Balance Scale score
Time Frame: Pre and Post 12 weeks
|
The Berg Balance Scale will be used to evaluate balance capability
|
Pre and Post 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Timed up and Go test
Time Frame: Pre and Post 12 weeks
|
Timed up and Go test will be used to assess functional mobility, dynamic balance, and fall risk in older adults
|
Pre and Post 12 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Dr. Mariam Salem, BMC
Publications and helpful links
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Balance and covid 19
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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