NCT03098719

Brief Summary

GISMO combines spatial information with findings on the health effects of sustainable, active forms of mobility in the work environment in order to derive evidence-based decision-making bases for a health-promoting, operational mobility management. Existing approaches - with regard to spatial information systems, decision-support systems and health effects of active mobility - are considered and supplemented by our developments and investigations. Achieved non-personal results are provided through standardized web interfaces, ensuring integration into existing and prospective tools of an innovative and health-promoting mobility management.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2017

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 18, 2017

Completed
2 days until next milestone

Study Start

First participant enrolled

March 20, 2017

Completed
15 days until next milestone

First Posted

Study publicly available on registry

April 4, 2017

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2018

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2019

Completed
Last Updated

March 4, 2020

Status Verified

March 1, 2020

Enrollment Period

1.3 years

First QC Date

March 18, 2017

Last Update Submit

March 3, 2020

Conditions

Outcome Measures

Primary Outcomes (1)

  • Cardiorespiratory Fitness, i.e. metaboloic equivalents (METs)

    Ergometry

    1 year

Secondary Outcomes (1)

  • Cardiovascular Risk

    1 year

Study Arms (2)

Intervention

EXPERIMENTAL
Behavioral: Active Mobility

Control

NO INTERVENTION

Interventions

Active MobilityBEHAVIORAL

see detailed discription

Intervention

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • employees of SALK (possibly also employees of other companies), age 18-70 voluntary participation in the study, consent in German language, desire to change the currently prevailing passive mobility behavior.

You may not qualify if:

  • physical or psychological condition that makes the participation and completion of the study unlikely. i.e.:
  • Participation in further clinical trials at the same time, or at least four weeks time
  • Pregnancy or lactation
  • Well-known diseases of the movement apparatus, which could influence healthy mobility
  • Subjects with osteoporosis requiring treatment
  • Severe general disease (e.g., neoplasia, tuberculosis, heart failure)
  • Subjects with chronic infections
  • subjects with alcohol or drug abuse or dependency

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Sports Medicine, Prevention and Rehabilitation Paracelsus Medical University

Salzburg, 5020, Austria

Location

MeSH Terms

Conditions

Health Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Medicine

Study Record Dates

First Submitted

March 18, 2017

First Posted

April 4, 2017

Study Start

March 20, 2017

Primary Completion

June 30, 2018

Study Completion

October 30, 2019

Last Updated

March 4, 2020

Record last verified: 2020-03

Data Sharing

IPD Sharing
Will not share

Locations