ClinicalTrials.Veeva

Menu

Evaluation of the Dynamic Work Intervention for Office Workers to Reduce Sedentary Behaviour

A

Amsterdam UMC, location VUmc

Status

Completed

Conditions

Lifestyle-related Condition

Treatments

Other: Dynamic Work

Study type

Interventional

Funder types

Other

Identifiers

NCT03115645
DynamicWork

Details and patient eligibility

About

Long-term sitting has been associated with multiple health risks. To reduce sitting time for office workers in a Dutch insurance company, an intervention will be implemented. The goal of this study is to evaluate this intervention on the short term (3 months) and long-term (12 months).

Full description

Large volumes of sitting time have been associated with multiple health risks such as diabetes, heart disease and premature death. Especially, in office workers sitting time per day can accumulate to over 10 hours a day. To reduce sitting time for office workers in a Dutch insurance company, an intervention will be implemented. The intervention contains the introduction of alternative workstations, intervention sessions with an occupational physiotherapist and an activity tracker with a self-help program booklet. The goal of this study is to evaluate the (cost) effectiveness of this intervention on the short term (3 months) and long-term (12 months). The primary outcome is objectively assessed sitting time.

In a cluster randomized controlled trial 250 employees of an insurance company will participate in the study. After baseline measurements, matched departments will be randomly assigned to the control or intervention group. The evaluation includes an economic and process evaluation.

Enrollment

244 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Employed by the insurance company for at least the duration of the study (12 months)
  • Employed at least 28 hours per week
  • Employed at one of the participating departments

Exclusion criteria

  • Already access to the Dynamic Working Intervention
  • Unable to stand or walk for longer time periods (i.e. wheelchair bound)
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

244 participants in 2 patient groups

Intervention group
Experimental group
Description:
Participants in the intervention group will receive the Dynamic Working Intervention program, as described in the next section.
Treatment:
Other: Dynamic Work
Control group
No Intervention group
Description:
Participants in the control group will not receive any intervention and will perform their work in the same manner as before.

Trial contacts and locations

4

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems