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OpenTrials
Completed

NCT Number: NCT01287208

Be Fit in Residency: a Randomized Controlled Trial of an Activity Device Among Medicine Residents

The main objective of this study is to test an intervention to increase the physical activity of medical residents, an employee population with little time for exercise. Specifically, the aims of this study are:

1. To determine if providing medical residents with an activity device that measures steps, distance, and calories burned and tracks this information over time on a website increases residents' physical activity levels as measured by number of steps per day compared to a control group using a blinded activity device (no feedback). 2. To determine if an unblinded team competition using the activity device directly following the randomized phase increases residents' activity level compared to baseline. 3. To determine if activity level is associated with change in weight during the residency year. 4. To determine if the average hours of sleep per week is associated with changes in weight and with activity level.

Completed

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Key information

Age range

21 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Massachusetts General Hospital medicine resident

Exclusion criteria

  • none

Treatment and study plan

Activity monitor

Device

The activity monitor is an accelerometer that records steps, distance, calories, and sleep

Other names: Fitbit

Activity device

Device

Accelerometer that has all the steps, distance, calories, and sleep data blinded to the study subject

Other names: Fitbit

Primary outcomes

  1. Steps Per Day

    Time frame: 12 weeks

    Steps will be recorded on the activity device

Secondary outcomes

  1. Distance Per Day

    Time frame: 12 weeks

    Distance in miles recorded on activity device.

  2. Calories Burned Per Day

    Time frame: 12 weeks

    Total calories burned per day recorded on activity device. This secondary outcome was not measured in the trial.

  3. Weight

    Time frame: 6 months

  4. Hours of Sleep Per Night

    Time frame: 12 weeks

    Number of hours slept per night as recorded on activity device.

    This secondary outcome was not measured in the trial.

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Feb 1, 2011
Registry last updated
Dec 7, 2017

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.

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