DivAirCity Social Health Survey (DivAirCitySH)

February 15, 2024 updated by: Andreas Michalsen, Charite University, Berlin, Germany

Anonymous Survey Among Local Residents on the Impact of the Planned Measures in the Five Partner Cities of the DivAirCity Project on Their Social Life, Health and Well-being

To reduce stress among urban residents, the consortium members of the European Council Horizon 2020 research program DivAirCity install different stress reducing, noise reducing and air quality improving means in the five cities of the consortium. This study measures physiological and psychological stress and health factors before and after the implementation of the project (at intervention sites) and compares the change (improvement) to the change in comparable places where no means were installed (control site).

Study Overview

Detailed Description

Scientific studies show that increased stress can favor the development of e.g. high blood pressure, heart disease, mental illness, infectious diseases, headaches and sleep disorders. This means that stress causes considerable costs for western healthcare systems, including in our city and this neighbourhood. In large cities, where there are often hardly any natural green and forest areas left, depression and anxiety syndromes, for example, are more common than among the rural population.

For example, in Germany, more than three quarters of the population live in densely or moderately populated areas, while the global average is more than 50 per cent. Due to increasing urbanisation, people living in cities will be heavily dependent on urban nature, which can be a relevant health-promoting factor. Several studies have shown that natural spaces such as city parks, parks and even greenery on streets have a positive impact on the health of residents, both individually and collectively.

The European Council Horizon 2020 project DivAirCity (acronym explanation in the text below) is about making formerly busy public spaces in European cities more attractive again for residents and citizens. The aim is to redesign the spaces in such a way that people of different age groups, social classes and identities ("Div") can (once again) come together and meet in these places on a daily basis. To this end, these places are to be changed through various installations (planting trees, redesigning parks, shading, watering in summer) in such a way that the local air quality ("Air") in the cities ("City") improves significantly. This is realized on the one hand by installing air quality measuring equipment and by recording the number of people and the time they spend in these places (objective measurements).

In addition to these objective measurements, this study records the impact on psychological and physiological health that the installations (intervention) has on the residents. To this end, it will be measured how residents feel in terms of quality of life, current stress, general health, and whether they feel safe and secure in the specific place (comfort, safety and security) and whether they enjoy going there and staying there,. These measurements will take place both before (day -60 to day -30) and after (day +30 and day +60) the installment of the intervention.

Finally, we would like to know your age group, your gender and how close you live to the location of the conversion/installation. We would like to invite you to take part in this survey again after the remodelling project.

Study Type

Observational

Enrollment (Estimated)

1000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Berlin, Germany, 14109
        • Recruiting
        • Charité -- Universitaetsmedizin Berlin
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Residents of the five cities (18+ years of age)

Description

Inclusion Criteria:

  • Participants must live or work at or near the installation (intervention group) or control site (control group)

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Aarhus, installation site
Residents of Aarhus (DK), living at or nearby the site of the installed Intervention
A number of means to reduce traffic noise and traffic exhausts and improve air quality will be implemented at designated urban spaces (intervention sites), while other places with comparable amount of traffic and no such changes will serve as control sites.
Aarhus, control site
Residents of Aarhus (DK), living at or nearby the control site
Bucharest, intervention site
Residents of Bucharest (RO), living at or nearby the site of the installed Intervention
A number of means to reduce traffic noise and traffic exhausts and improve air quality will be implemented at designated urban spaces (intervention sites), while other places with comparable amount of traffic and no such changes will serve as control sites.
Bucharest, control site
Residents of Bucharest (RO), living at or nearby the control site
Castelló, intervention site
Residents of Castelló (ES), living at or nearby the site of the installed Intervention
A number of means to reduce traffic noise and traffic exhausts and improve air quality will be implemented at designated urban spaces (intervention sites), while other places with comparable amount of traffic and no such changes will serve as control sites.
Castelló, control site
Residents of Castelló (ES), living at or nearby the control site
Orvieto, intervention site
Residents of Orvieto (IT), living at or nearby the site of the installed Intervention
A number of means to reduce traffic noise and traffic exhausts and improve air quality will be implemented at designated urban spaces (intervention sites), while other places with comparable amount of traffic and no such changes will serve as control sites.
Orvieto, control site
Residents of Orvieto (IT), living at or nearby the control site
Potsdam, intervention site
Residents of Potsdam (DE), living at or nearby the site of the installed Intervention
A number of means to reduce traffic noise and traffic exhausts and improve air quality will be implemented at designated urban spaces (intervention sites), while other places with comparable amount of traffic and no such changes will serve as control sites.
Potsdam, control site
Residents of Potsdam (DE), living at or nearby the control site

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
WHO-5 Well-being Scale
Time Frame: Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
Validated Questionnaire
Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Kessler K6 psychological distress
Time Frame: Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
Validated Questionnaire
Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
ASKU questionnaire
Time Frame: Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
Validates Questionnaire for self-efficacy
Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Questionnaire for General Physiological Health
Time Frame: Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
Custom-made Questionnaire
Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
Questionnaire about feelings of safety and security at the site
Time Frame: Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented
Custom-made Questionnaire
Baseline: 60 to 30 days before the installation implementation vs Posttest: 30 to 60 days after the installation has been implemented

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

February 20, 2024

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

February 2, 2024

First Submitted That Met QC Criteria

February 15, 2024

First Posted (Estimated)

February 23, 2024

Study Record Updates

Last Update Posted (Estimated)

February 23, 2024

Last Update Submitted That Met QC Criteria

February 15, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EA4/252/23

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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