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Completed

NCT Number: NCT01501994

Personalized Approach for Promoting Physical Activity in Mayo Clinic Physicians

The purpose of the study is to determine if providing physicians with a walking workstation, exercise counseling, and accelerometer feedback about activity will increase physician activity.

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Key information

Age range

25 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

20 physicians will be given an activity monitoring accelerometer (GRUVE from MUVE, inc.) for 2 weeks prior to starting the study (without feedback) and will continue to have their activity monitored for the duration of the study. The accelerometer (monitors movement and accurately estimates physical activity energy expenditure). The physicians will be randomized to 12 weeks with accelerometer monitoring but no feedback or counseling (control) or to 12 weeks of accelerometer monitoring (experimental) with feedback about activity levels and 20 minute weekly counseling sessions on how to increase activity (including walking while working). In the 12 week period where physicians receive feedback and counseling, they will also be provided a walking workstation. The walking workstation (assembled by the investigators) has a computer keyboard, computer monitor and telephone attached to an exercise treadmill. This allows the user to walk at 1 mile per hour while dictating, typing, responding to e-mail, etc. The treadmill can be placed in an examining room if the physician wishes to use it while dictating notes or it can be placed in a separate office.

Those physicians assigned to monitoring only for the first 12 weeks will then receive monitoring plus feedback, counseling, and walking workstation use for the next 12 weeks. Those physicians assigned to feedback, counseling, and walking workstation use for the first 12 weeks will continue to receive accelerometer feedback but will no longer receive counseling or use a walking workstation for the subsequent 12 weeks.

Ten physicians will complete the above for the first 26 weeks of the study and 10 physicians will complete the above for the last 26 weeks of the study.

The time line of the study is as follows:

12 Wks Experimental → 12 Wks Control 10 MDs (Wk 1-26) → 2 wks Monitor 12 Wks control → 12 Wks Experimental

12 Wks Experimental → 12 Wks Control 10 MDs (Wk 27-52) → 2 wks Monitor 12 Wks control → 12 Wks Experimental

In summary, physicians use an accelerometer without feedback while in the control group. In the experimental group physicians receive three interventions: accelerometer with feedback, exercise counseling, and the use of a walking workstation (treadmill desk).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Physicians working in the Department of Medicine at Mayo Clinic Rochester
  • Age 25 to 70 years
  • BMI > 25
  • Sedentary (exercise for 30 minutes less than 3 times weekly)

Exclusion criteria

  • Metastatic cancer
  • Unable to complete a Bruce protocol exercise stress test
  • Planning on retiring in the next 6 months
  • Planning on more than 3 weeks of vacation during the 6 month study
  • Women of child-bearing age who are pregnant or planning on becoming pregnant.

Treatment and study plan

GRUVE accelerometer (MUVE, inc.)

Other

Physicians in the experimental group will be given an accelerometer for 2 weeks (without feedback) prior to starting the study and will continue to have their activity monitored for the duration of the study. The accelerometer monitors movement and accurately estimates physical activity energy expenditure. They will receive feedback about their activity for the remainder of the trial. Physicians in the control group will wear the accelerometer but not receive feedback for the first 14 weeks of the trial. They will receive feedback for the last 12 weeks of the trial as they crossover to the experimental group.

walking workstation

Other

The physicians in the experimental group will be provided with a walking workstation. The walking workstation has a computer keyboard, computer monitor and telephone attached to an exercise treadmill (assembled by the investigators). This allows the user to walk at 1 mile per hour while dictating, typing, responding to e-mail, etc. The treadmill can be placed in an examining room if the physician wishes to use it while dictating notes or it can be placed in a separate office. For the last 12 weeks of the study the experimental group will not use the walking workstation while the control grop will use the workstation (crossover).

Other names: treadmill desk

exercise counseling

Procedure

After the first two weeks of baseline data collection, the experimental group will receive exercise counseling for the next 12 weeks. They will be advised to make use of the accelerometer and the walking workstation as well as how to increase their activity in other ways. This group will not receive exercise counseling for the last 12 weeks of the study while the control group will cross over and receive exercise counseling for the last 12 weeks of the study (the control group will not receive exercise counseling for the first 14 weeks of the study).

Primary outcomes

  1. Activity units determined by accelerometer

    Time frame: 26 weeks

Secondary outcomes

  1. weight in kilograms

    Time frame: 26 weeks

  2. Maximal oxygen consumption (VO2 max)

    Time frame: 26 weeks

    Fitness as determined by an oxygen consumption treadmill test

  3. Percent body fat determined by bone density scan (DEXA)

    Time frame: 26 weeks

  4. Fasting glucose

    Time frame: 26 weeks

  5. Hemoglobin A1c

    Time frame: 26 weeks

  6. Fasting insulin

    Time frame: 26 weeks

  7. Fasting lipid profile

    Time frame: 26 weeks

  8. high sensitivity c-reactive protein

    Time frame: 26 weeks

  9. Well Being using National Center for Health Statistics (NCHS) Well Being Scale

    Time frame: 26 weeks

  10. Depression by Center for Epidemiologic Studies Depression (CES-D) Scale

    Time frame: 26 weeks

  11. Linear Analog Self Assessment Scale

    Time frame: 26 weeks

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Dec 30, 2011
Registry last updated
Jun 6, 2014

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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