- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07719816
Qualitative Study of Student Financial Insecurity and Psychiatry (QUALIPEPSY)
A Qualitative Exploration of the Impact of Financial Insecurity on the Development of Psychiatric Disorders and the Use of Healthcare Services Among Students
Since the COVID-19 pandemic, mental health disorders have increased significantly, particularly among young people. In France, the proportion of young people aged 18 to 25 suffering from depression almost doubled between 2017 and 2021. This phenomenon particularly affects students, who are already identified as being at greater risk of mental health disorders than the general population. Medical students seem to be particularly vulnerable: in 2021, a national study showed very high rates of depression and suicidal thoughts in this population. The main factor associated with depression was the feeling of financial hardship.
Students often face multiple forms of insecurity. Financially, they have limited resources and struggle to cover their basic needs such as housing, food and healthcare. Socially, many experience significant isolation, particularly when they are away from their families or under pressure from their studies. All of this has a significant impact on their mental health. Unfortunately, many students do not seek help due to lack of time, resources, or awareness of support services. The 2021 study showed that only one-third of medical students suffering from depression received appropriate treatment.
The aim of the study is to explore the lived experiences of the students concerned in order to identify what they perceive as the various aspects of student precarity (housing, transport, isolation, financial difficulties, etc.) and the links they perceive between these and their psychological distress. This study will deepen our understanding of these factors by exploring students' lived experiences, and will bring to light elements not identified by quantitative studies.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Marie BENHAMMANI-GODARD
- Phone Number: 0033158411190
- Email: marie.godard@aphp.fr
Study Contact Backup
- Name: Cédric LEMOGNE, MC, PhD
- Phone Number: 0033 1 42 34 85 76
- Email: cedric.lemogne@aphp.fr
Study Locations
-
-
IDF
-
Paris, IDF, France, 75014
- Adult Psychiatry Department - Hôtel-Dieu Hospital
-
Contact:
- Cédric LEMOGNE, MD, PhD
- Phone Number: 0033 1 42 34 85 76
- Email: cedric.lemogne@aphp.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- A student enrolled at Paris Sciences et Lettres (PSL) University or the Faculty of Health Sciences at Université Paris Cité (UPC),
- Aged 18 or over,
- Fluent in French,
- be a student,
- have used the PPOP scheme,
- not object to participating after receiving clear information.
Exclusion Criteria:
- Participants under the age of 18,
- not enrolled at PSL universities or the UPCS Faculty of Health Sciences,
- insufficient proficiency in French to conduct an interview,
- refusal to participate,
- clinical vulnerability deemed incompatible by the referring consultant.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients
Students
|
Semi-structured interviews
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Semi-structured interview
Time Frame: Day of inclusion
|
This is an exploratory, inductive qualitative study.
The aim is not to measure but to explore and understand these students' lived experiences, without any preconceived assumptions
|
Day of inclusion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Semi-structured interview
Time Frame: Day of inclusion
|
This is an exploratory, inductive qualitative study.
The aim is not to measure but to explore and understand these students' lived experiences, without any preconceived assumptions
|
Day of inclusion
|
Collaborators and Investigators
Collaborators
Investigators
- Study Chair: Ariel FRAJERMAN, MD, Institut National de la Santé Et de la Recherche Médicale, France
- Study Director: Jordan SIBEONI, MD, PhD, Institut National de la Santé Et de la Recherche Médicale, France
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- APHP260752 - QUALIPEPSY
- 2026-A01287-44 (Other Identifier: France : Ministry of Health)
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
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.
Clinical Trials on Depressive Disorder
-
Aalborg University HospitalRecruitingDepressive Disorder | Depression | Depressive Episode | Depressive Disorders | Depressive Episodes | Depression - Major Depressive Disorder | Depressive Disorder, Major Depressive DisorderDenmark
-
Sheba Medical CenterNot yet recruiting
-
Rotman Research Institute at BaycrestRecruitingMajor Depressive Disorder (MDD)Canada
-
ACADIA Pharmaceuticals Inc.RecruitingACP-211 Monotherapy for Major Depressive Disorder With Inadequate Antidepressant Response (NORLIGHT)Depressive Disorder, Treatment-Resistant | Major Depressive Disorder (MDD)United States
-
The Royal Ottawa Mental Health CentreNot yet recruitingDepression | Major Depressive Disorder (MDD) | Depressive Episode | Depression - Major Depressive DisorderCanada
-
Stanford UniversityNational Institute of Mental Health (NIMH)Recruiting
-
TakedaRecruitingMajor Depressive DisorderJapan
-
Neurocrine BiosciencesRecruitingMajor Depressive DisorderSpain, Serbia, United States, Bulgaria, Canada, Estonia, Italy, Poland, Taiwan, Australia, South Korea
-
Luye Pharma Group Ltd.Enrolling by invitationMajor Depressive DisorderChina
-
NeuroQore Inc.Makromed Inc.Enrolling by invitationMajor Depressive DisorderUnited States
Clinical Trials on Semi-structured interviews
-
Indiana UniversityPatient-Centered Outcomes Research InstituteCompletedColorectal Cancer ScreeningUnited States
-
Institut Paoli-CalmettesNot yet recruiting
-
Assistance Publique - Hôpitaux de ParisURC-CIC Paris Descartes Necker CochinCompletedChronic (Non-malignant) Musculoskeletal PainFrance
-
Region SkaneLund UniversityCompletedSuicidal Ideation | Self-Harm, Deliberate | Self Injurious Behavior Without Suicidal IntentSweden
-
University of New MexicoSociety of Family PlanningWithdrawnPregnancy TerminationUnited States
-
Fundació Institut de Recerca de l'Hospital de la...UnknownChemotherapy-induced AlopeciaSpain
-
University of NimesNot yet recruitingCancer Colorectal | Hypnosis, AnimalFrance
-
Hospices Civils de LyonActive, not recruitingAdult Patients Managed in a Cardiac Critical Care Unit With a Pathology Requiring at Least One Potentially Painful and Anxiety-provoking Invasive ProcedureFrance
-
The Royal Orthopaedic Hospital NHS TrustCompletedGreater Trochanteric Pain SyndromeUnited Kingdom
-
Hospices Civils de LyonCompletedStroke | Breast Cancer | AsthmaFrance