NCT02071420

Brief Summary

Our objective in this pilot study is to test the combined effect of a) replacing office workers' sedentary workstations with active workstations (LifeBalance Station) and b) optimizing computer workstation ergonomics on daily occupational sedentary time, cardiometabolic risk factors, musculoskeletal symptom health outcomes and work productivity.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2014

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2014

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

February 21, 2014

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 25, 2014

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2014

Completed
3.3 years until next milestone

Results Posted

Study results publicly available

October 23, 2017

Completed
Last Updated

October 23, 2017

Status Verified

September 1, 2017

Enrollment Period

6 months

First QC Date

February 21, 2014

Results QC Date

August 24, 2015

Last Update Submit

September 20, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Occupational Physical Activity From Baseline to 16 Weeks

    Occupational physical activity (primary outcome) will be measured objectively with the GENEActiv physical activity monitor. The monitor will be worn on the right ankle and will be worn for 5 working days during all non-bathing hours. The outcome measure will be change in occupational activity (average counts/work day) from baseline to 16 weeks. The measure will be calculated as follows: 16 weeks value - baseline value.

    Baseline and 16 weeks

Study Arms (2)

Experimental Group

EXPERIMENTAL

This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.

Behavioral: Active Workstation InterventionBehavioral: Ergonomic InterventionBehavioral: Email InterventionDevice: Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application.

Active Control

ACTIVE COMPARATOR

This group will receive the ergonomic intervention and email intervention only for 16 weeks. This group will not receive a seated active workstation.

Behavioral: Ergonomic InterventionBehavioral: Email InterventionDevice: Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application.

Interventions

Participants in the experimental group will receive a seated active workstation at their work setting for 16 weeks.

Experimental Group

Participants of both arms will receive a face to face ergonomic workstation optimization intervention. This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.

Active ControlExperimental Group

Participants of both arms will receive three emails per week for 16 weeks. Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).

Active ControlExperimental Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • We will recruit overweight/obese (body mass index 25.0-40.0 kg/m2) adults (18-65 years) working in full-time (minimum 35 hours/week), sedentary (self-report sitting \>75% work time) occupations at an independent work site.

You may not qualify if:

  • Working in an office that will not meet the space or electrical requirements of the active workstation, acute or chronic illness not under treatment of a provider, orthopedic limitations that prohibit physical activity, current or planned pregnancy, hospitalization from a physical or mental disorder in the past six months and/or taking medication that may impair physical activity

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Iowa

Iowa City, Iowa, 52242, United States

Location

Related Publications (1)

  • Carr LJ, Leonhard C, Tucker S, Fethke N, Benzo R, Gerr F. Total Worker Health Intervention Increases Activity of Sedentary Workers. Am J Prev Med. 2016 Jan;50(1):9-17. doi: 10.1016/j.amepre.2015.06.022. Epub 2015 Aug 7.

MeSH Terms

Conditions

Sedentary BehaviorOverweight

Condition Hierarchy (Ancestors)

BehaviorOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Results Point of Contact

Title
Lucas Carr, PhD
Organization
University of Iowa

Study Officials

  • Lucas Carr, PhD

    University of Iowa

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

February 21, 2014

First Posted

February 25, 2014

Study Start

January 1, 2014

Primary Completion

July 1, 2014

Study Completion

July 1, 2014

Last Updated

October 23, 2017

Results First Posted

October 23, 2017

Record last verified: 2017-09

Locations