A Study of the Effectiveness of FitBit Use to Increase Physical Activity in the Medical Workplace
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 15-003049
NCT ID: NCT02794727
Sponsor Protocol Number: 15-003049
About this study
The purpose of this study is to assess if providing sedentary workers a FitBit® and physical activity goals will lead to an increase in occupational physical activity. It is believed that measures of emotional health will also improve. Decreased physical activity is not only associated with multiple chronic medical conditions, including obesity, but also with depressed mood, and other negative emotions. As many employed adults spend a great deal of time at work where they are mostly sedentary, strategies to increase physical activity at work are being pursued to help improve the physical and mental health of Americans.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Between 18 - 65 years of age
- A Mayo Clinic employee at 0.75 FTE or more
- Have not used an activity monitor within 2 weeks of study entry
- Agrees not use any other activity monitor during study participation
- Not pregnant by subject self report
- Have a stable weight - defined as self-reported weight that has not changed more than 10% in the past 3 months
- Not have any previous history of joint problems that limit free movement, as determined by the PI
- Able to participate fully in all aspects of the study
- Have understood and signed study informed consent
Exclusion Criteria:
- Have a known history of any condition or factor judged by the investigator to preclude participation in the study or which might hinder adherence or skew data collection - such as a position where they predominantly provide transport as part of their job
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
Mayo Clinic Location |
Status |
|
Rochester, Minn.
Mayo Clinic principal investigator Sanjeev Nanda, M.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available