- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04364100
Experience of Hospital Students in the Odontology Department (EQUAVECU)
April 24, 2020 updated by: University Hospital, Brest
Qualitative Study of the Experience of Hospital Students in the Odontology Department
During their studies, the dental students of Brest (France) learn their future profession by working in the Dental University Hospital, from the fourth academic year.
This clinical activity is considered as both a source of satisfaction and stress by most of the students.
The main objective of this study is to investigate the experience of Brest dental students through a qualitative methodology, with individual interviews, followed by an analysis by grounded theory (Paillé, 1994).
Study Overview
Status
Completed
Conditions
Detailed Description
During their studies, the dental students of Brest (France) learn their future profession by working in the Dental University Hospital, from the fourth academic year.
This clinical activity is considered as a source of satisfaction by most of the students.
They are also reassured because they know that they will easily find an employment at the end of their studies.
However, the clinical activity can also create a stress among the students, which varies with their progress in their studies (Polychronopoulou et Divaris, 2009).
Other sources of stress could also be identified.
This multifactorial stress can influence their well-being, their practices and their relationships with patients.
The stress and satisfactions of the dental students have mainly been studied by some questionnaires (Inquimbert et al., 2017).
The main objective of this study is to investigate the experience of Brest dental students through a qualitative methodology, with individual interviews, followed by an analysis by grounded theory (Paillé, 1994).
This type of research can enable us to keep a broad approach of students' experience and to stay faithful to it.
Study Type
Observational
Enrollment (Actual)
12
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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Brest, France, 29200
- CHRU de Brest
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Volunteer students of Brest Dental University Hospital in fourth, fifth and sixth academic year
Description
Inclusion Criteria:
- volunteer students of Brest Dental University Hospital, having given his/her consent
- adult students of Brest Dental University Hospital, in fourth, fifth and sixth academic year
Exclusion Criteria:
- students in work-stoppage
- students in Erasmus program
- non-volunteer students or students refusing to give his/her consent
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 |
|---|---|---|
|
Evaluation of the hospital student (4th, 5th, 6th years) in odontology
Time Frame: 1 to 2 months
|
Data collection until saturation: no new information after two consecutive interviews (theorizing)
|
1 to 2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Valérie Chevalier, CHRU de Brest
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)
February 19, 2020
Primary Completion (Actual)
March 3, 2020
Study Completion (Actual)
March 3, 2020
Study Registration Dates
First Submitted
March 9, 2020
First Submitted That Met QC Criteria
April 24, 2020
First Posted (Actual)
April 27, 2020
Study Record Updates
Last Update Posted (Actual)
April 27, 2020
Last Update Submitted That Met QC Criteria
April 24, 2020
Last Verified
April 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 29BRC19.0255
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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