- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03356613
GenI: a Tool to Generate Paramedical Research Ideas (GenI)
November 23, 2017 updated by: Central Hospital, Nancy, France
In order to develop paramedical research culture, the paramedical staff need adapted tools and methods.
The GenI project (Research ideas generation) has for main objective the design and validation of a tool that will allow the identification of paramedical research ideas.
This tool will be built based on paramedical staff views.
Our hypothesis is that the use of the GenI tool will help to detect research ideas in paramedical health care that could lead to research projects.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
52
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
-
-
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Vandœuvre-lès-Nancy, France, 54500
- CIC 1433 Epidémiologie clinique
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-
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
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
paramedical staff
Description
Inclusion Criteria:
- paramedical staff working in one of the 4 hospitals involved in the study
Exclusion Criteria:
- paramedical staff with a research degree
- paramedical staff that are paramedical coordinator in the hospital
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 |
|---|---|
|
focus group of paramedical staff from Nancy
During the focus group, the psychologist researcher asks the group a series of question about their views and opinions on research and how to make it.
|
An researcher in psychology will lead focus group on research views for paramedical staff
|
|
focus group of paramedical staff from Metz
During the focus group, the psychologist researcher asks the group a series of question about their views and opinions on research and how to make it.
|
An researcher in psychology will lead focus group on research views for paramedical staff
|
|
focus group of paramedical staff from Dijon
During the focus group, the psychologist researcher asks the group a series of question about their views and opinions on research and how to make it.
|
An researcher in psychology will lead focus group on research views for paramedical staff
|
|
focus group of paramedical staff from Bar-le-Duc
During the focus group, the psychologist researcher asks the group a series of question about their views and opinions on research and how to make it.
|
An researcher in psychology will lead focus group on research views for paramedical staff
|
|
Test of the tool by paramedical staff center 1
Paramedical staff who didn't participate to the focus group, will test the GenI tool to generate research ideas.
|
The GenI tool built on paramedic's view will be tested.
|
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Test of the tool by paramedical staff center 2
Paramedical staff who didn't participate to the focus group, will test the GenI tool to generate research ideas.
|
The GenI tool built on paramedic's view will be tested.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of the number of research ideas generated by a group of experts and by a group of paramedical staff
Time Frame: in 1 year
|
At the end of each focus group, the group of paramedical staff and the group of experts will provide the list of ideas generated with or without the use of the tool.
The number of ideas will be counted
|
in 1 year
|
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Comparison of the pertinence of research ideas generated by a group of experts and by a group of paramedical staff
Time Frame: in 1 year
|
Each research idea will be evaluated by an independent expert group on the "utility, innovation and feasibility" aspects (likert in 4 points) in order to compare the research ideas generated by paramedical groups (with the support of the GENI tool) and the research ideas generated by research experts groups.
|
in 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sylvie Klein, Chru Nancy Brabois
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 15, 2017
Primary Completion (ANTICIPATED)
April 1, 2018
Study Completion (ANTICIPATED)
December 1, 2018
Study Registration Dates
First Submitted
November 16, 2017
First Submitted That Met QC Criteria
November 23, 2017
First Posted (ACTUAL)
November 29, 2017
Study Record Updates
Last Update Posted (ACTUAL)
November 29, 2017
Last Update Submitted That Met QC Criteria
November 23, 2017
Last Verified
November 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- APPARA2016/GENI-KLEIN/ER
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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