NCT02146482

Brief Summary

The purpose of the study is to evaluate the changes in back pain from access to a sit-stand workstation. Other muscle and joint pain and/or discomfort will also be evaluated. We hypothesize that access to a sit-stand workstation will allow one to experience postural variation and reduce back pain.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
57

participants targeted

Target at P25-P50 for not_applicable low-back-pain

Timeline
Completed

Started Apr 2013

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

Study Start

First participant enrolled

April 1, 2013

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2013

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2014

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

May 21, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 23, 2014

Completed
1.1 years until next milestone

Results Posted

Study results publicly available

June 19, 2015

Completed
Last Updated

November 6, 2017

Status Verified

October 1, 2017

Enrollment Period

8 months

First QC Date

May 21, 2014

Results QC Date

May 18, 2015

Last Update Submit

October 6, 2017

Conditions

Keywords

back painlow back painsit-stand workstationstanding desk

Outcome Measures

Primary Outcomes (1)

  • Change in Back Pain

    The Roland-Morris Disability Questionnaire is designed to assess self-rated physical disability caused by low back pain. The patient is asked to agree or disagree with 24 different statements related to their back pain. The end score is the sum of the agreed statements. The score ranges from 0 (no disability) to 24 (maximum disability).

    Baseline (Week 1) and Follow-Up (Week 18)

Secondary Outcomes (1)

  • Change in Pain in Other Body Parts

    At the conclusion of each work day for 12 weeks and 8 weeks later

Study Arms (2)

Control

NO INTERVENTION

Did not receive an intervention during the active portion of the study (i.e. 12 weeks). After the active portion of the study, this group was given a sit-stand computer workstation.

Sit-stand computer workstation

EXPERIMENTAL

Given a sit-stand computer workstation to use at their place of work

Other: Sit-stand computer workstation

Interventions

A sit-stand computer workstation allows one to sit or stand throughout the day while maintaining continued use of one's computer.

Also known as: Standing desk, WorkFit
Sit-stand computer workstation

Eligibility Criteria

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

You may qualify if:

  • Back pain lasting ≥3 months and reported at a minimum of 4 out of 10 on the pain scale.
  • Sits \>6 hours out of an 8-hour work day for work purposes
  • Able and willing to fill out a daily survey for the first week prior to randomization
  • Participants must be \>18 years of age. There are no gender/race-ethnic restrictions.
  • Ability to understand and the willingness to sign a written informed consent document.

You may not qualify if:

  • Unable to stand for at least 10 minutes.
  • Currently using a sit-stand desk

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Stanford, California, 94305, United States

Location

Related Publications (45)

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MeSH Terms

Conditions

Low Back PainBack Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Results Point of Contact

Title
Grant Ognibene
Organization
Stanford University

Study Officials

  • Kathleen C Horst, MD

    Stanford University

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

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

Study Record Dates

First Submitted

May 21, 2014

First Posted

May 23, 2014

Study Start

April 1, 2013

Primary Completion

December 1, 2013

Study Completion

March 1, 2014

Last Updated

November 6, 2017

Results First Posted

June 19, 2015

Record last verified: 2017-10

Locations