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Health Care Provider Preventiomter Study

Sponsor
Mayo Clinic (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05387590
Collaborator
(none)
90
Enrollment
1
Location
1
Arm
7
Anticipated Duration (Months)
12.9
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate health care providers' perceptions, ratings and motivation to adopt a novel and state of the art physical wellness assessment device, the Preventiometer.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Preventiometer device with wellness coaching
 N/A

Detailed Description

The Preventiometer is a physical wellness tool that assesses multiple physical wellness measurements in a 60 +/- 15 minute period of time.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Health Care Providers Perceptions, Ratings and Motivation to Adopt/Utilize a Novel and State of the Art Physical Wellness Assessment Device (Preventiometer)
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
May 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Preventiometer Device

The Preventiometer is a physical wellness tool that assesses multiple physical wellness measures in a 60 ± 15 minutes period of time. It is intended to promote population wellness by empowering individuals to act upon the information they receive about their overall health.

Behavioral: Preventiometer device with wellness coaching
Four wellness coaching sessions with a certified wellness coach to develop and implement your own personalized wellness plan will be included in this study.

Outcome Measures

Primary Outcome Measures

  1. Likert scale questionnaire on Preventiometer Wellness Assessment [1 day]

    Health care providers perception of the Preventiometer Wellness Device.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

  • Health care providers practicing at Mayo Clinic.

  • Able to speak English and complete surveys.

  • Able to read, understand and sign inform consent.

Exclusion Criteria:

  • Unable to sign inform consent.

  • Pregnant women. (As verbalized by participant).

  • Unable to ambulate without assistance.

  • Not currently involved in another formal program or research study involving wellness coaching.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Rochester Rochester Minnesota United States 55901

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Brent Bauer, MD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Brent A. Bauer, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT05387590
Other Study ID Numbers:
  • 21-011313
First Posted:
May 24, 2022
Last Update Posted:
Aug 1, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 1, 2022