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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04130932
Other study ID # 19-006733
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 1, 2020
Est. completion date December 31, 2021

Study information

Verified date October 2021
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Researchers are trying to better understand how offices and workspaces influence people's performance, behavior and health during the course of weeks and over long periods of time.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 31, 2021
Est. primary completion date July 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Ability to provide informed consent - Must be adults between the ages of 18 and 60 - Ability to relocate to the Well Living Lab for 9 consecutive weeks - Full-time Mayo Clinic employees (35+ hours per week) - Report working a sedentary job (e.g., sit for >= 50% of their work time). - Have a working mobile phone that can receive text messages - Must be present for 80% of the study (minimum of 4 days per week) Exclusion Criteria: - Individuals who are shift-workers - Individuals diagnosed with vascular diseases (i.e., Raynaud's disease, peripheral artery disease, etc.) - Individuals with diagnosed neurological and psychiatric disorders that may have physical limitations - Drug (illegal or prescription narcotic), nicotine, or alcohol dependency - Women who are lactating, pregnant or intend to become pregnant during the duration of the study - Individuals who are taking medications (either prescribed or over-the-counter) which may affect comfort levels (e.g., opiate based medications) - Working in occupation requiring standing/stepping >50% of work time - Report < 1 year at current job - Hospitalization from either a physical or mental disorder in the past six months - History of cardiovascular, pulmonary, metabolic, neurological, or orthopedic limitations that would prohibit occupational physical activity (e.g., standing, stepping, etc.)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ergonomic flooring
Specially designed flooring system to optimize ergonomics of participants

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sickness, absence, presenteeism Work Limitations Questionnaire 9 weeks
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