Acceptability, Representations and Experiences of an Application and Captors Which Suggest a Walking Itinerary

NCT05984355 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2023-08-09

No results posted yet for this study

Summary

ParcourSenior is a project lead by School of Mines from Saint-Etienne, Gérontopôle AURA and "Senior Autonomie" to promote walking in a city environment. To enable that, we have two tools at your disposable. The first one is sensor which can measure physicals abilities. The second one is an application which proposes individual itineraries based on physical abilities. This application concern people whom want to walk alone, with supportive people or with new people encounter in this app. Both tools are in the process of being created. The current study focuses on needs, expectations and desire of the elders and professionals about both of these tools. After, we plan to focus on the acceptability of these devices. A qualitative study with focus groups is carried out to evaluate the needs and expectation follows by individual interviews to evaluate the project: acceptability, fears and use's perception.

Conditions

  • Aging

Interventions

OTHER

Individual interviews

Discussion between the searcher and the participant about representations and acceptability about a potential application and captors which suggest a Walking itinerary

Sponsors & Collaborators

  • Saint Etienne School of Mine

    collaborator OTHER
  • Senior Autonomie

    collaborator UNKNOWN
  • Centre Hospitalier Universitaire de Saint Etienne

    lead OTHER

Principal Investigators

  • Nathalie Barth, PhD · Gerontopole Auvergne Rhône Alpes

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05984355 on ClinicalTrials.gov