NCT03507764

Brief Summary

The principal objective of this study is to determine if the provision of a treadmill workstation in an emergency medical services (EMS) dispatch center increases the number of steps that participants make daily within 6 months compared to the usual working conditions. The investigators hypothesized that the provision of a treadmill workstation with a slow walking could increase the number of daily steps and decrease days of leave, musculoskeletal disorders without decreasing the dispatch quality.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2018

Typical duration 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

First Submitted

Initial submission to the registry

February 12, 2018

Completed
3 days until next milestone

Study Start

First participant enrolled

February 15, 2018

Completed
2 months until next milestone

First Posted

Study publicly available on registry

April 25, 2018

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2019

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2019

Completed
Last Updated

October 7, 2021

Status Verified

August 1, 2019

Enrollment Period

1.2 years

First QC Date

February 12, 2018

Last Update Submit

September 29, 2021

Conditions

Keywords

TreadmillsExerciseNumber of stepsDispatchers

Outcome Measures

Primary Outcomes (1)

  • Difference of number of steps at 0 and 6 months

    Number of daily steps measured by actimetry (including all walking activities measured over a day). Measurements will be done with actimetry during one week before the randomization and at 6 months

    0 and 6 months

Secondary Outcomes (13)

  • Evaluation of Quality of life

    0, 6 and 12 months

  • Evaluation of Anxiety and depression

    0, 6 and 12 months

  • Change in blood pressure

    0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 months

  • Change in heart rate

    0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 months

  • Change in Weight

    0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 months

  • +8 more secondary outcomes

Study Arms (2)

Control Group

NO INTERVENTION

During the randomized study phase (6 months),subjects will perform their usual activity without access to the treadmill workstation in the dispatch center. After six months, all subjects will continue to be assessed with free access to the treadmill workstation at the workplace.

Experimental Group

EXPERIMENTAL

During the randomized study phase, subjects will have an open access to the treadmill workstation with the indication to use it for at least one hour (continuous or split) on working days. After six months, all subjects will continue to be assessed with free access to the treadmill workstation.

Other: Use of the treadmill workstation at work

Interventions

During the randomized study phase, provision of the treadmill workstation with the recommendation to use it for at least one hour (continuous or split) during each of the working shifts. After six months, all subjects will use treadmill without restrictions or conditions.

Experimental Group

Eligibility Criteria

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

You may qualify if:

  • Dispatchers working in Emergency Medical Service

You may not qualify if:

  • Pregnant women
  • Inability to walk

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Grenoble

Grenoble, France

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Guillaume Debaty, MD, PhD

    CHU Grenoble Alpes, SAMU38

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 12, 2018

First Posted

April 25, 2018

Study Start

February 15, 2018

Primary Completion

May 15, 2019

Study Completion

December 31, 2019

Last Updated

October 7, 2021

Record last verified: 2019-08

Data Sharing

IPD Sharing
Will not share

Locations