- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06575608
Estimation of VO2Max Using Smartphone Application
Estimation of VO2Max Using Smartphone Application in Elderly: Validation Study
The aim of this observational study Is to examine the validity of the Smartphone application (VO2max calculator) in calculating VO2max in elderly population.
Research hypotheses:
this study will test the following null hypothesis: (Vo2max calculator) application will not have criterion validity in estimating VO2max values in the elderly population.
Research question:
Is the Smartphone application (VO2max calculator) considered a valid tool for estimating accurate values of VO2max in the elderly population in comparison to the golden standard method?
Study Overview
Status
Conditions
Detailed Description
Although maximal oxygen consumption (VO2max) is growing in evidence as a powerful indicator of several health conditions it's rarely used in clinical practice due to the high expense, requirement of specialized equipment, and related risks of maximal exertion. So, we aim to develop a simpler method for estimating VO2max using modern smartphone technologies.
Method: participants of this study will be divided into 2 equal groups. The first group will perform a gold standard treadmill-based VO2max measurement and the other group will perform a smartphone based 1-mile walk test for VO2max estimation.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Ghada said, Bachelor
- Phone Number: +201148571986
- Email: ghadasaid700@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Elderly subjects aged from (65 to 75) years.
- BMI 18.5-29.9 kg/m2
- Answer (NO) to all of the questions in the Physical activity readiness questionnaire (PAR-Q)
- Do not have any absolute or relative contraindications for exercise testing according to the American Heart Association (AHA) statement.
Exclusion Criteria:
- Recent surgical conditions.
- Skeletal deformities.
- Blood pressure regulating medication intake.
- Any respiratory disorders.
- Back, hip, knee or ankle pain within last month.
- Any neurological or psychiatric conditions.
- Implanted pacemaker.
- Anemic patients.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
direct VO2max test group
Group A (n-26) will perform a direct VO2max test on the treadmill and vo2max will be calculated by the cardiopulmonary exercise testing (CPX) device Spirometry Medisoft Ergocart professional.
|
|
1-mile walk test group
Group B (n-26) will perform the 1 mile walk test and VO2 max will be calculated by the smartphone application VO2max calculator
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
maximum oxygen consumption (VO2MAX)
Time Frame: at the peak of exercise (peak VO2) over the final 30 seconds of exercise
|
The greatest amount of oxygen a person can take in from inspired air while performing dynamic exercise involving a large part of total muscle mass.
|
at the peak of exercise (peak VO2) over the final 30 seconds of exercise
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate (HR)
Time Frame: at baseline one shot
|
the number of times your heart beats per minute.
|
at baseline one shot
|
|
The Borg rating of perceived exertion (RPE) scale
Time Frame: at baseline one shot
|
It is a subjective scale for estimating effort and exertion, breathlessness, and fatigue during physical work.
|
at baseline one shot
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
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
- P.T.REC/012/004899
Drug and device information, study documents
product manufactured in and exported from the U.S.
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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