Study Stopped
Unable to conduct study due to equipment not operational from study Sponsor team in Germany
Health Care Provider Preventiomter Study
Health Care Providers Perceptions, Ratings and Motivation to Adopt/Utilize a Novel and State of the Art Physical Wellness Assessment Device (Preventiometer)
1 other identifier
interventional
N/A
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started May 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 12, 2022
CompletedFirst Posted
Study publicly available on registry
May 24, 2022
CompletedStudy Start
First participant enrolled
May 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2025
CompletedJune 27, 2024
June 1, 2024
7 months
May 12, 2022
June 26, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Likert scale questionnaire on Preventiometer Wellness Assessment
Health care providers perception of the Preventiometer Wellness Device.
1 day
Study Arms (1)
Preventiometer Device
OTHERThe 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.
Interventions
Four wellness coaching sessions with a certified wellness coach to develop and implement your own personalized wellness plan will be included in this study.
Eligibility Criteria
You may qualify if:
- Health care providers practicing at Mayo Clinic.
- Able to speak English and complete surveys.
- Able to read, understand and sign inform consent.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mayo Cliniclead
Study Sites (1)
Mayo Clinic Rochester
Rochester, Minnesota, 55901, United States
Related Links
Study Officials
- PRINCIPAL INVESTIGATOR
Brent Bauer, MD
Mayo Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 12, 2022
First Posted
May 24, 2022
Study Start
May 1, 2024
Primary Completion
December 1, 2024
Study Completion
January 1, 2025
Last Updated
June 27, 2024
Record last verified: 2024-06