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Clinical Trials/NCT06493006
NCT06493006
Recruiting
Not Applicable

Impact of Physically Active Versus Passive Way to Work on Physical and Mental Aspects of Health in Members at Hannover Universities: an Observational Study

Hannover Medical School1 site in 1 country500 target enrollmentAugust 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mobility on the Way to Work and Health-related Outcomes
Sponsor
Hannover Medical School
Enrollment
500
Locations
1
Primary Endpoint
Heart rate variability (HRV)
Status
Recruiting
Last Updated
5 months ago

Overview

Brief Summary

The aim of the study is to assess health data (heart rate variability, blood pressure, blood glucose, particulate matter pollution) and travel characteristics (length, duration and type of commute) on the way to and from work from members of the universities in Hannover (Germany).

Detailed Description

Active mobility, (i.e. moving around using the own physical strength) has positive sustainability effects. The physically active way to and from college is a great untapped resources for health promotion. The aim of this sub-project is to examine the way to university in order to assess its effect on individual health depending on the means of transport. In order to determine the status quo and changes in mobility behavior the investigators will use movement trajectories using smartphone apps or inexpensive trackers in a larger cohort, as well as more specified health measures including overweight status, blood pressure, blood glucose concentration, lack of exercise, particulate matter and risk of accidents in a smaller sub-cohort. By linking this data with the personal characteristics surveyed in other sub-projects, an evaluation of the individual health status and the expected health benefits depending on the route to work can be created. This represents the database for identifying certain groups of people or status groups who could particularly benefit from targeted promotion of an active commute.

Registry
clinicaltrials.gov
Start Date
August 1, 2024
End Date
June 30, 2026
Last Updated
5 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • living within 50km around the workplace

Exclusion Criteria

  • current participation in another interventional study

Outcomes

Primary Outcomes

Heart rate variability (HRV)

Time Frame: 24 hours on two separate days for the short-term subgroup, and 7 consecutive days for the long-term subgroup

HRV measured by a wearable activity tracker

Secondary Outcomes

  • Blood glucose concentration(24 hours on two separate days for the short-term subgroup)
  • Work-Ability-Index(Once at baseline for both study subgroups)
  • 24 hour blood pressure(24 hours on two separate days for the short-term subgroup)
  • Daily moderate to vigorous physical activity (MVPA) duration(7 consecutive days for the long-term subgroup)
  • Health-related quality of life(Once at baseline for both study subgroups)
  • Particulate matter(24 hours on two separate days for the short-term subgroup)

Study Sites (1)

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