- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03273361
Desk Cycling Work Performance Evaluation
March 20, 2018 updated by: Liza Rovniak, Milton S. Hershey Medical Center
Desk-Compatible Elliptical Device: Feasibility Evaluation
This lab study is evaluating the feasibility of accomplishing productive office work while simultaneously pedaling a compact desk-based cycling device.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
96
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18-65 years
- Ability to type without looking at the keyboard
- Native English speaker
- Normal hearing
- Spend 6 or more hours per day sitting
- Less than 150 minutes of physical activity per week
Exclusion Criteria:
- Positive response on the Physical Activity Readiness Questionnaire indicating that low intensity pedaling could present safety risks
- Pregnancy
- Body mass index less than 18 or greater than 35
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Seated
Participants completed work tasks while seated.
|
Participants pedaled a compact cycling device while simultaneously working at a desk.
|
|
Experimental: Low Intensity Pedaling
Participants completed work tasks while pedaling at a low intensity.
|
Participants pedaled a compact cycling device while simultaneously working at a desk.
|
|
Experimental: Low-Moderate Intensity Pedaling
Participants completed work tasks while pedaling at a low-moderate intensity.
|
Participants pedaled a compact cycling device while simultaneously working at a desk.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Typing task
Time Frame: 5 minutes
|
Participants completed a computerized typing task
|
5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reading task
Time Frame: 5 minutes
|
Participants read a brief passage and answered questions to assess reading comprehension.
|
5 minutes
|
|
Logic Reasoning and Phone Task
Time Frame: 5 minutes
|
Participants completed logical reasoning questions while answering a simulated phone call.
|
5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Liza Rovniak, PhD, MPH, Pennsylvania State University College of Medicine
- Study Director: Andris Freivalds, PhD, Penn State University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2016
Primary Completion (Actual)
September 1, 2017
Study Completion (Actual)
September 1, 2017
Study Registration Dates
First Submitted
September 1, 2017
First Submitted That Met QC Criteria
September 1, 2017
First Posted (Actual)
September 6, 2017
Study Record Updates
Last Update Posted (Actual)
March 21, 2018
Last Update Submitted That Met QC Criteria
March 20, 2018
Last Verified
March 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00001535
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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