- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06609655
AgeTeQ Database Management Framework
AgeTeQ Database Management Framework "Arts, Health and New Information and Communication Technologies"
The AgeTeQ "Arts, health and new information and communication technologies (NICTs)" laboratory database contains all the clinical and paraclinical data of participants in clinical research projects carried out by the AgeTeQ laboratory on the themes of the arts, and/or health, and/or NICTs.
The database can thus contain quantitative data (i.e. non-invasive measurements taken with questionnaires or measuring devices providing numerical values such as blood pressure, heart rate or electrical activity of the brain, etc.) and qualitative data (i.e. extracted from a verbatim in the context of guided interviews) from participants in the above-mentioned clinical research projects. These data can take the form of spreadsheets containing numerical values, written documents such as verbatims, and audio or video recordings.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Olivier Beauchet, MD PhD
- Phone Number: 3637 514 340 3540
- Email: olivier.beauchet@umontreal.ca
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Had participate to a previous research project managed by the administrator of the databank
- Agreed to integrated the databank
Exclusion Criteria:
- Less than 18 years old
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
adults
Adults 18 years old and more, male and female, having participated in one research project and agreeing that data are integrated in the databank
|
The AgeTeQ database "Arts, health and new information and communication technologies" has three objectives. The first is to preserve the data collected as part of the research projects carried out by the AgeTeQ laboratory. The second objective of the database is to use the information provided by the recorded data to fuel reflection, test new research hypotheses and thus open up new avenues of research for the Arts, Health and New Information and Communication Technologies research team. The third objective is to share the AgeTeQ database with the scientific community on a non-commercial basis, to improve access to data on the themes of arts, health and new technologies, and to increase knowledge and enable the development of research in these fields. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Preserve the data collected as part of the research projects carried out by the AgeTeQ laboratory
Time Frame: 20 years
|
To centralized harmonize data from different protocols in the field of interest
|
20 years
|
|
Analyze the data collected as part of the research projects carried out by the AgeTeQ laboratory
Time Frame: 20 years
|
To analyze data to fuel reflection, test new research hypotheses and thus open up new avenues of research for the Arts, Health and New Information and Communication Technologies
|
20 years
|
|
Share the data collected as part of the research projects carried out by the AgeTeQ laboratory
Time Frame: 20 years
|
To improve access to data on the themes of arts, health and new technologies, and to increase knowledge and enable the development of research in these fields.
|
20 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2025-227
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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