- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05745402
Longitudinal Study to Determine the Effectiveness of the Mobility Checkup for Older Adults (LEMCOA)
A Longitudinal Study of the Effectiveness of the Mobility Checkup for Older Adults: Feasibility in the 'Year 1' Cohort
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Healthy aging is defined as "the process of developing and maintaining the functional ability that enables well-being in older age" and includes mobility. Mobility disability (i.e., the inability to walk 400 meters and climb a flight of stairs without assistance) is the most prevalent form of disability for older adults in the United States. Unlike blood pressure or body mass index, physical performance measures such as walking speed help identify and predict preclinical mobility disability, but are rarely used in routine medical care. This is a missed opportunity, particularly for older adults, who may experience a subtle decline in physical performance that leads to mobility disability.
The position of the American Physical Therapy Association is that all people should have an annual physical therapy visit to optimize movement and promote health, wellness, and fitness; and slow the progression of impairments of body functions and structures, activity limitations, and participation restrictions.
Recommendations support preventive care for maintaining mobility. However, a model of care specific to preventing mobility disability in older adults is not common practice. Evidence suggests routine screening can predict mobility disability in older adults and that activity-based interventions prevent it.
The is year 1 of a longitudinal study that will determine the feasibility of an effectiveness study of a Mobility Checkup, an annual preventive visit within a model of physical therapy care. The Mobility Checkup prioratizes educating older adults on the value of physical performance as an indicator of health and aims to maintain mobility and reduce mobility disability among participants. Ultimately, this new model of care could result in a cost-effective tool to establish baseline physical performance and identify and prevent preclinical and mobility disabilities in older adults.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Alexandra L Borstad, PhD
- Phone Number: 218-625-4938
- Email: aborstad@css.edu
Study Locations
-
-
Minnesota
-
Duluth, Minnesota, United States, 55812
- Recruiting
- College of St. Scholastica-Health Science Center
-
Contact:
- Kathy King, BS
- Phone Number: 218-723-6786
- Email: kking@css.edu
-
Contact:
- John D Borstad
- Phone Number: 2187236523
- Email: jborstad1@css.edu
-
Principal Investigator:
- Alexandra L Borstad, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 55 years of age or older
- Walk independently with or without an assistive device
Exclusion Criteria:
- Experiencing short-term condition affecting their mobility
- Cardiac procedure or myocardial infarction (heart attack) in the last 6 months
- Has a guardian who is responsible for their healthcare decisions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mobility Checkup Intervention
45-minute Mobility checkup that includes 5 physical performance measures and education based on outcomes compared to age and gender normative values.
|
The Mobility Checkup (MC) for older adults is a 45-minute preventative physical therapy visit designed to maintain mobility during aging.
It has two parts, measurement (25 minutes) and education (20 minutes).
The 5 standardized measures of physical performance in the MC are Walking speed, single leg stance time (balance), Five rep sit to stand (muscular endurance, transitions), 6-meter walk test (general endurance), and Timed up from floor test (transitions).
Participants are provided education structured into 4 elements.
1.
They are told their performance scores 2. They are shown how their performance scores on each of the measures compare to age and sex-referenced normative values 3.
They are provided information about what their performance predicts about their health 4.
They are referred to an appropriate provider if there was a health or safety concern during their MC or they are educated to follow the recommendations for physical activity that are recommended by the CDC.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
LASA Physical Activity Questionnaire (LAPAQ)
Time Frame: one year
|
Questionnaire designed to measure the amount of physical activity a person completed over the last two weeks.
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The 6-minute walk test
Time Frame: one year
|
In the 6-minute walk test the distance in meters a person can walk in 6 minutes is measured as evidence of their endurance.
|
one year
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- 1234 (Department of Defense)
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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