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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02109432
Other study ID # PBRC 2013-051
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date July 2015

Study information

Verified date March 2019
Source Pennington Biomedical Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this investigation is to evaluate participant use of a dedicated office pedal desk with and without behavioral support.


Description:

For this pilot study the investigators will identify and recruit up to 20 full time Pennington Biomedical staff members employed in sedentary jobs (i.e., report mostly sitting during working hours). The sample size is limited by the number of pedal desks being built for this pilot study and the need for timely data generation. Although the investigators can stagger starts as needed, all participants must intend to be on campus for the subsequent 6 weeks after they start the intervention. Two cohorts of 10 participants will complete the three 2-week conditions in the following order: 1) SELF-DIRECTED use where participants have access to their daily recorded data but will not have any other form of feedback or goal-setting; 2) FACILITATED use where participants are provided with their daily recorded pedal desk data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount; 3) FACILITATED use with PEDOMETER where participants will be provided with their daily recorded pedal desk and step count data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount and increase their step count by 3,000 steps/day compared to baseline. Participants will be asked to pedal at a sustainable and self-selected pace while using the pedal desk.


Recruitment information / eligibility

Status Terminated
Enrollment 7
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria:

- Be a full-time employee at Pennington Biomedical Research Center

- Be between 21 and 65 years of age

- Primarily sit while at work

- Work from a private office/cubicle

Exclusion Criteria:

- Weigh more than 250 pounds

- Have physical limitations that prevent performance of pedaling motions

- Plan to be away from work for the 6 weeks of the intervention

- Be pregnant

- Have a pace maker and/or metal joint replacement

- Plan to be away from work for the 6 weeks of the intervention

Study Design


Related Conditions & MeSH terms

  • Physical Activity in the Workplace

Intervention

Behavioral:
Self-Directed Pedal Desk
participants will have a pedal desk installed in their office and will have access to their daily recorded data but will not have any other form of feedback or goal-setting
Facilitated Pedal Desk
participants are provided with their daily recorded pedal desk data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount
Facilitated Pedal Desk with Pedometer
participants will be provided with their daily recorded pedal desk and step count data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount and increase their step count by 3,000 steps/day compared to baseline.

Locations

Country Name City State
United States Pennington Biomedical Research Center Baton Rouge Louisiana

Sponsors (1)

Lead Sponsor Collaborator
Pennington Biomedical Research Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight Change (kg) KG weight change from Baseline to 6 weeks Baseline to 6 weeks