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Enrolling by invitationNCT07472569TrustAndMoveUpdated Jul 30, 2026

Trust in Institutions, Environment, and Physical Activity

An observational study in Physical Activity Attitude, Health Behavior and Trust, sponsored by University Hospital, Clermont-Ferrand. Enrolling by invitation at 1 site in France. Open to participants aged 16 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-30.

Sponsored by University Hospital, Clermont-Ferrand · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
2,000
Ages
16 Years and older
Sex
All
01

Study summary

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.

Read the 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.).

02

Conditions studied

  • Physical Activity Attitude
  • Health Behavior
  • Trust

Keywords

  • Physical activity
  • Sedentary behavior
  • Trust
  • Environment
  • Institutions
  • Climate
  • Government
  • WHO recommendation
  • Pollution alert
  • Extreme heat alert
03

In context

Health Behavior

967 studies on the registry are indexed under Health Behavior; 165 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 219 across 131 observational studies indexed under Health Behavior.

Browse Health Behavior studies →

Lead sponsor

University Hospital, Clermont-Ferrand is the lead sponsor of 859 studies on the registry; 179 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Worldwide

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Anyone willing to participate.

Exclusion criteria

Exclusion Criteria:

  • Refusal to participate in the study is equivalent to not completing the self-administered questionnaire.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
2,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Level of trust on physical activity recommendation

    Level of trust on institutions regarding physical activity recommendations will be assessed using a questionnaire. It will be measured using Visual Analog Scale (VAS) from (0) "don't trust at all" to (100) "trust a lot".

    Time frame: Day 1

Secondary outcomes

  1. Sociodemographic characteristics

    Age, gender, country of residence, education level, ethnicity collected using questionnaire

    Time frame: Day 1

  2. Professional characteristics

    Professional status, employment sector collected usijng questionnaire.

    Time frame: Day 1

  3. Anthropometric measure

    Body Mass Index (BMI - kg/m²) calculated from self-reported height (cm) and weight (kg).

    Time frame: Day 1

  4. Lifestyle factors

    Smoking status, alcohol consumption, physical activity level collected using questionnaire.

    Time frame: Day 1

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2025 (actual). Primary completion is estimated for Dec 2027, 32 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 10, 2026
First posted
Mar 16, 2026
StartActual
Apr 3, 2025
Primary completionEst.
Dec 2027
CompletionEst.
Dec 2050
Last update
Jul 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07472569
Responsible party
Sponsor
First posted
Mar 16, 2026
Start date
Apr 3, 2025
Primary completion
Dec 2027 (estimated)
Completion
Dec 2050 (estimated)
Last update
Jul 30, 2026

Study contacts

Frédéric Dutheil
principal investigator · University Hospital, Clermont-Ferrand

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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