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Clinical Trials/NCT03115645
NCT03115645
Completed
Not Applicable

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

Amsterdam UMC, location VUmc1 site in 1 country244 target enrollmentJanuary 23, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lifestyle-related Condition
Sponsor
Amsterdam UMC, location VUmc
Enrollment
244
Locations
1
Primary Endpoint
Sitting time
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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).

Detailed 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.

Registry
clinicaltrials.gov
Start Date
January 23, 2017
End Date
April 18, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amsterdam UMC, location VUmc
Responsible Party
Principal Investigator
Principal Investigator

H. P. Van der Ploeg

Associate Professor

Amsterdam UMC, location VUmc

Eligibility Criteria

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

Outcomes

Primary Outcomes

Sitting time

Time Frame: Change in sitting time between baseline and 12 month follow up assessment

Total sitting time will be measured objectively with the activPAL activity tracker

Secondary Outcomes

  • Occupational sitting time(Assessed at baseline 3 months and 12 months)
  • Non-occupational sitting time(Assessed at baseline 3 months and 12 months)
  • Occupational stepping time(Assessed at baseline 3 months and 12 months)
  • Non-occupational stepping time(Assessed at baseline 3 months and 12 months)
  • Sitting time in bouts of 30 min(Assessed at baseline 3 months and 12 months)
  • Need for recovery(Assessed at baseline 3 months and 12 months)
  • Sitting, physical activity and work related outcomes(Assessed at baseline 3 months and 12 months)
  • Process evaluation(Assessed at 3 months and 12 months)
  • Quality of life measured with EQ-5D-5L(Assessed at baseline 3 months and 12 months)
  • Occupational sitting time in bouts of 30 min(Assessed at baseline 3 months and 12 months)
  • Total standing time(Assessed at baseline 3 months and 12 months)
  • Total stepping time(Assessed at baseline 3 months and 12 months)
  • Non-occupational sitting time in bouts of 30 min(Assessed at baseline 3 months and 12 months)
  • Musculoskeletal complaints(Assessed at baseline 3 months and 12 months)
  • Sitting time in bouts of 60 min(Assessed at baseline 3 months and 12 months)
  • Occupational standing time(Assessed at baseline 3 months and 12 months)
  • Non-occupational standing time(Assessed at baseline 3 months and 12 months)
  • Occupational sitting time in bouts of 60 min(Assessed at baseline 3 months and 12 months)
  • Waist circumference and body height(Assessed at baseline 3 months and 12 months)
  • Individual Work Performance(Assessed at baseline 3 months and 12 months)
  • Effort-reward imbalance(Assessed at baseline 3 months and 12 months)
  • Non-occupational sitting time in bouts of 60 min(Assessed at baseline 3 months and 12 months)
  • Body weight(Assessed at baseline 3 months and 12 months)
  • Vitality(Assessed at baseline 3 months and 12 months)
  • Absenteeism(Assessed at baseline 3 months and 12 months)
  • Healthcare consumption(Assessed at 3 months and 12 months)

Study Sites (1)

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