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OpenTrials
Completed

NCT Number: NCT02794727

Physical Activity in the Medical Workplace

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 we are predominantly sedentary, strategies to increase physical activity at work are being pursued to help improve the physical and mental health of Americans. This 17 week randomized controlled trial will investigate changes of occupational physical activity in three groups: those provided with a FitBit® but not able to monitor their activity level, and those provided with activity goals and individual physical activity challenges, and those who do not use a FitBit®.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

About this study

All subjects will be entered into a 4 week run-in phase where subjects will wear a blinded Fitbit during work hours. The baseline work activity is collected at this time. This phase is followed by a randomization to one of 3 groups: the blinded Fitbit group, the unblinded Fitbit group, and the group which will not wear any activity monitors. During these 12 weeks we will collect data on activity levels during work hours. Everyone will have a final contact at week 17 to close out the study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be between 18 - 65 years of age
  • Be a Mayo Clinic employee at 0.75 FTE or more
  • Have no previous use of any activity monitor for 14 consecutive days or more
  • Not be 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
  • Be 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.

Treatment and study plan

Blinded Fitbit

Device

Subjects will wear a blinded Fitbit to monitor activity while in the workplace for 12 weeks.

Unblinded Fitbit

Device

Subjects will be unblinded to the Fitbit display for 12 weeks with set activity goals.

Primary outcomes

  1. Change in Fitbit Step Count Per Day

    Time frame: Baseline through Week 16

    change in number of daily steps as measured by the fitbit monitor

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Physical Activity in the Medical Workplace- a Way to Improve Physical and Mental Well-being?

Acronym: OPA

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Jun 9, 2016
Registry last updated
Apr 29, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.