Trust in Institutions, Environment, and Physical Activity (TrustAndMove)

March 13, 2026 updated by: University Hospital, Clermont-Ferrand
Trust is the willingness of people to cooperate. Although much research has been conducted on physical activity, little research has explored trust in institutions regarding environmental and physical activity recommendations. This study aims to assess the level of trust in sources of physical activity recommendations as well as to determine the factors that may influence trust in sources of physical activity recommendations, such as environmental, sociodemographic, or lifestyle factors.

Study Overview

Status

Enrolling by invitation

Conditions

Detailed Description

Cross-sectional observational study using an online self-administered questionnaire (RedCAP). Flyers with the QR code/link to the questionnaire will be distributed 1) electronically by email via institutional mailing lists of employees/agents, social networks, blogs, internet advertisements, etc. and 2) in paper format in all locations likely to increase the number of respondents (sports facilities, public or private establishments, supermarkets and places of consumption, etc.). The questionnaire is quick and easy to complete (5 to 10 minutes), and participation is voluntary. The study is completely anonymous. No identifying data will be collected (no email address, no date of birth, etc.).

Study Type

Observational

Enrollment (Estimated)

2000

Contacts and Locations

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

Study Locations

  • France
      • Clermont-Ferrand, France
        • CHU de Clermont-Ferrand

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Worldwide

Description

Inclusion Criteria:

  • Anyone willing to participate.

Exclusion Criteria:

  • Refusal to participate in the study is equivalent to not completing the self-administered questionnaire.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Level of trust on physical activity recommendation
Time Frame: Day 1
Level of trust on institutions regarding physical activity recommendations will be assessed using a questionnaire
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Factors influencing trust on institutions
Time Frame: Day 1
Age, gender, country, education, professional status, sector activity, ethnicity, BMI, lifestyle factors will be assessed using a questionnaire.
Day 1

Collaborators and Investigators

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

Sponsor

University Hospital, Clermont-Ferrand

Investigators

  • Principal Investigator: Frédéric Dutheil, CHU de Clermont-Ferrand

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 (Actual)

April 3, 2025

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

December 1, 2050

Study Registration Dates

First Submitted

March 10, 2026

First Submitted That Met QC Criteria

March 13, 2026

First Posted (Actual)

March 16, 2026

Study Record Updates

Last Update Posted (Actual)

March 16, 2026

Last Update Submitted That Met QC Criteria

March 13, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2026_Dutheil (Trust and Move)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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