NCT03052426

Brief Summary

The aim of this study is to combat the growing global health issue of sedentary behavior and the associated health consequences of prolonged sitting in the workplace. The population of desk-based workers makes up a relatively large population and are an important target for this health promoting initiative with a focus on improving posture, encouraging movement, and fostering a more active and healthy business community. It's important to recognize that occupational therapy practitioners can contribute to community health promotion/disease prevention programs by the skill-set of practitioners to understand habits and routines that influence the adoption and maintenance of healthy behaviors.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
18

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2017

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 8, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 14, 2017

Completed
13 days until next milestone

Study Start

First participant enrolled

February 27, 2017

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 27, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 27, 2017

Completed
1.4 years until next milestone

Results Posted

Study results publicly available

January 14, 2019

Completed
Last Updated

January 14, 2019

Status Verified

January 1, 2019

Enrollment Period

6 months

First QC Date

February 8, 2017

Results QC Date

October 11, 2018

Last Update Submit

January 11, 2019

Conditions

Outcome Measures

Primary Outcomes (2)

  • Reported Musculoskeletal Discomfort Per Group at 3 Months

    Three scales were compiled 1) aches and pains, 2) discomfort and 3) interference due to aches and pains. All three scales included 9 questions centered on the occurrence in body regions, including the neck, shoulder, upper and lower back, upper arms, forearm/wrist, hip, thigh, and knee/lower leg. Aches and Pains was on a 5 point scale, from 1) Never to 5) Several Times a Day. Uncomfortable was on a 4 point scale, ranging from 0) No Discomfort to 3) Very Uncomfortable. Interference was on a 4 point scale from 0) Not a problem to 3) Substantially interfered. Higher scores indicated more problems in each of these areas.

    3 months

  • Reported Musculoskeletal Discomfort Per Group at 6 Months

    Three scales were compiled 1) aches and pains, 2) discomfort and 3) interference due to aches and pains. All three scales included 9 questions centered on the occurrence in body regions, including the neck, shoulder, upper and lower back, upper arms, forearm/wrist, hip, thigh, and knee/lower leg. Aches and Pains was on a 5 point scale, from 1) Never to 5) Several Times a Day. Uncomfortable was on a 4 point scale, ranging from 0) No Discomfort to 3) Very Uncomfortable. Interference was on a 4 point scale from 0) Not a problem to 3) Substantially interfered. Higher scores indicated more problems in each of these areas.

    6 months

Secondary Outcomes (1)

  • Reported Musculoskeletal Discomfort at Work at 3 Months and 6 Months All Groups Combined

    Beginning of study, 3 months, and 6 months (end of study)

Study Arms (3)

30 Minute Group

ACTIVE COMPARATOR

This group will use the Ergotron WorkFit-TL (a sit to stand work station) and be required to alternate periods of sitting and standing every 30 minutes throughout their workday.

Device: Ergotron WorkFit - TL

60 Minute Group

ACTIVE COMPARATOR

This group will use the Ergotron WorkFit-TL (a sit to stand work station) and be required to alternate periods of sitting and standing every 60 minutes throughout their workday.

Device: Ergotron WorkFit - TL

90 Minute Group

ACTIVE COMPARATOR

This group will use the Ergotron WorkFit-TL (a sit to stand work station) and be required to alternate periods of sitting and standing every 90 minutes throughout their workday.

Device: Ergotron WorkFit - TL

Interventions

A sit to stand work station.

30 Minute Group60 Minute Group90 Minute Group

Eligibility Criteria

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

You may qualify if:

  • Participants must spend \> 50% of their work day seated at the computer
  • Participants must be primarily English speaking
  • Participants must work within the Health Sciences Center building at West Virginia University

You may not qualify if:

  • Participants who are less than 18 years of age
  • Participants who are not primarily English speaking
  • Participants who spend \<50% of their work day seated at the computer
  • Participants who do not work within the Health Sciences Center building at West Virginia University
  • Participants who are pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

West Virginia University

Morgantown, West Virginia, 26506, United States

Location

MeSH Terms

Conditions

Musculoskeletal PainSedentary Behavior

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsBehavior

Limitations and Caveats

Number of participants per group were small creating decreased power for study results between groups.

Results Point of Contact

Title
Dr. Brandy Brown
Organization
West Virginia University

Study Officials

  • Brandy Brown, OTD

    West Virginia University

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

February 8, 2017

First Posted

February 14, 2017

Study Start

February 27, 2017

Primary Completion

August 27, 2017

Study Completion

August 27, 2017

Last Updated

January 14, 2019

Results First Posted

January 14, 2019

Record last verified: 2019-01

Data Sharing

IPD Sharing
Will not share

There is not a plan to share individual participant data.

Locations