Assessing the Effects Of Treadmill On LPA, Sitting Time, and Cardiovascular Risk
1 other identifier
interventional
15
1 country
1
Brief Summary
The purpose of this study is to:
- 1.Evaluate the relative efficacy of a treadmill desk intervention on light physical activity and sitting behaviors at work over four weeks;
- 2.Evaluate the relative efficacy of a treadmill desk intervention on the cardiovascular risk profiles (blood pressure, body weight, body fat percentage) over a four-week period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 27, 2017
CompletedFirst Posted
Study publicly available on registry
August 2, 2017
CompletedStudy Start
First participant enrolled
October 5, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 7, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 8, 2019
CompletedJanuary 7, 2020
January 1, 2020
1.2 years
July 27, 2017
January 6, 2020
Conditions
Outcome Measures
Primary Outcomes (3)
Time spent sitting
The change in time spent sitting as measured by the ActivPAL, from baseline to the final week of each intervention condition
7-days
Time spent standing
The change in time spent standing as measured by the ActivPAL, from baseline to the final week of each intervention condition
7-days
Time spent moving
The change in time spent moving as measured by the ActivPAL, from baseline to the final week of each intervention condition
7-days
Secondary Outcomes (3)
Cardiovascular risk: Blood pressure
7-days
Cardiovascular risk: Body weight
7-days
Cardiovascular risk: Percent body fat
7-days
Study Arms (2)
Usual Desk
NO INTERVENTIONparticipants will work at their usual desk for four weeks.
Treadmill desk
EXPERIMENTALParticipants will be asked to use a treadmill desk for a minimum of 30 minutes per day for four weeks (Participants will sign up for a total of 30 minutes each day). Additional time may be spent on the treadmill, time permitting (two treadmills will be available to up to 10 people over the four week period).
Interventions
A standing height desk with a treadmill attached.
Eligibility Criteria
You may qualify if:
- Not currently pregnant or planning to become pregnant during the 11 week study period.
- Able to read and write in English.
- No current use of a sit/stand or treadmill desk.
- Work that is done in a predominately stationary position.
- Working at UMN West Bank Office Building at least 30 hours per week.
- Not currently meeting physical activity guidelines.
- No balance issues (i.e. healthy vestibular system)
- No contraindications to standing or walking
- Weight stable for the past 12 months.
- Taking no more than 3 prescription drugs, with stable dosage, over the past 12 months
- Answer of no to all Physical Activity Readiness-Questionnaire (PAR-Q) questions
You may not qualify if:
- Currently pregnant or actively trying to become pregnant during the 14 week study period.
- Unable to read and write in English.
- Working less than 30 hours per week.
- Currently meeting physical activity guidelines.
- Non-sedentary job.
- Current use of treadmill desk
- Any reported balance problems
- Anyone with contraindications to standing or walking
- Weight fluctuations of more than +/- 10% of their body weight in the past year
- Individuals taking more than 4 prescription drugs and/or unstable dosage of medications over the past 12 months if taking 3 or less.
- Answer of yes to any PAR-Q questions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Minnesota West Bank Office Building
Minneapolis, Minnesota, 55454, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 27, 2017
First Posted
August 2, 2017
Study Start
October 5, 2018
Primary Completion
December 7, 2019
Study Completion
December 8, 2019
Last Updated
January 7, 2020
Record last verified: 2020-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, ICF, CSR, ANALYTIC CODE
- Time Frame
- Data will become available within 6 months of study completion.
- Access Criteria
- Data access requests will be reviewed by the Principal Investigator. Requestors will be required to sign a data access agreement.
Deidentified IPD for all primary and secondary outcome measures will be made available upon request.