- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT04374643
Descriptive Study of the PSYchological Impact of CONFinement Measures in the General Population (PsyConfPop)
Descriptive Study of the PSYchological Impact of CONFinement Measures in the General Population : PsyConfPop
Quarantine is an unpleasant experience : separation from loved ones, loss of freedom, uncertainty about infection status, boredom. It may lead to negative mental health consequences and thus the emergence of anxiety and depressive symptoms.
From March 17th, 2020 to May 11th 2002, the French government has implemented national containment measures due to the Covid-19 epidemic.
Although there are data on the psychological impact and experience of quarantine measures in people who have been infected or suspected of being carriers of certain pathogens (e.g. Ebola), there are no data on such impact in the French population and quarantines lasting longer than 21 days. Investigators therefore propose to conduct a human and social sciences study in order to better understand the current situation
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
The main objective is to describe the psychological state during confinement (and the impact of the confinement) in a sample of the French general population.
Secondary objectives :
- to assess the evolution of psychological health between the period of confinement and post-confinement.
- to identify clinical factors modulating psychological state during confinement
It is expected to highlight :
- a link between the intensity of anxiety symptoms and the number/quality of social contacts
- a reduction of anxiety and depression symptoms in the post-confinement period.
- higher consumption of drugs during the confinement period
Self-questionnaires (Google form format) are sent by mailing lists or social networks to participants in order to complete the assessment of psychological state. A unique identifier is sent in a separate email. These assessments are performed at least once during the confinement period. It is planned to repeat them when the confinement is lifted: 15 days, 3 and 6 months after the lifting of the confinement because of the risk of developing anxiodepressive symptoms, in particular post-traumatic stressors.
Studietype
Inschrijving (Verwacht)
Contacten en locaties
Studie Locaties
-
-
-
Montpellier, Frankrijk, 34295
- Werving
- University Hospital
-
Contact:
- Catherine GENTY, MD
- Telefoonnummer: +33 4 67 99 61 45 75
- E-mail: c-genty@chu-montpellier.fr
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
Beschrijving
Inclusion criteria:
- age> 18
Exclusion criteria:
- protective measure (curatorship, guardianship)
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
---|---|
Confined patients
General population
|
Questionnaires to assess the psychological impact of confinement and its evolution over 6 months
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Depressive Symptomatology
Tijdsspanne: during confinement
|
depressive symptomatology with Patient Health Questionnaire : PHQ-9 scale (PHQ 9 higher score, more depressive -> min : 0 max : 27)
|
during confinement
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Depressive Symptomatology
Tijdsspanne: post-confinement : 15 days, 3 months, 6 months
|
depressive symptomatology with Patient Health Questionnaire : PHQ-9 scale (PHQ 9 higher score, more depressive -> min : 0 max : 27)
|
post-confinement : 15 days, 3 months, 6 months
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Psychological pain
Tijdsspanne: during confinement
|
Psychological pain : likert scale (higher score, more psychological pain-> min : 0 max : 10)
|
during confinement
|
sleep
Tijdsspanne: during confinement
|
quality of sleep assessed with Insomnia Seveity Index (ISI Insomnia Severity Scale ; higher score, more insomnia -> min : 0 max : 28)
|
during confinement
|
sleep
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
quality of sleep assessed with Insomnia Seveity Index (ISI Insomnia Severity Scale ; higher score, more insomnia -> min : 0 max : 28)
|
post-confinement (15 days, 3 months, 6 months)
|
anxiety
Tijdsspanne: during confinement
|
anxiety intensity assessed by Generalized Anxieety Disorder (GAD 7 Generalized Anxiety Disorder higher score, more anxious -> min : 0 max : 21)
|
during confinement
|
anxiety
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
anxiety intensity assessed by Generalized Anxieety Disorder (GAD 7 Generalized Anxiety Disorder higher score, more anxious -> min : 0 max : 21)
|
post-confinement (15 days, 3 months, 6 months)
|
psychological pain
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
psychological pain : likert scale (higher score, more psychological pain-> min : 0 max : 10)
|
post-confinement (15 days, 3 months, 6 months)
|
physical pain
Tijdsspanne: during confinement
|
psychological pain : likert scale (higher score, more psychological pain-> min : 0 max : 10)
|
during confinement
|
physical pain
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
psychological pain : likert scale higher score, more psychological pain-> min : 0 max : 10)
|
post-confinement (15 days, 3 months, 6 months)
|
anger
Tijdsspanne: during confinement
|
staxi state scale (STAXI ; State and Trait Anger Expression Inventory : higher score, more anger -> min : 0 max : 50)
|
during confinement
|
anger
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
staxi state scale (STAXI ; State and Trait Anger Expression Inventory : higher score, more anger -> min : 0 max : 50)
|
post-confinement (15 days, 3 months, 6 months)
|
Stressful Event Impact
Tijdsspanne: during confinement
|
Assessed by the Stressful Event Impact Scale - Horowitz (HOROWITZ higher score, more traumatizes -> min : 0 max : 45) ) |
during confinement
|
Stressful Event Impact
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
Assessed by the Stressful Event Impact Scale - Horowitz (HOROWITZ higher score, more traumatizes -> min : 0 max : 45)
|
post-confinement (15 days, 3 months, 6 months)
|
Use of psychotropic drugs
Tijdsspanne: during confinement
|
Number of patients declaring an increase of psychotropic drug use
|
during confinement
|
Use of psychotropic drugs
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
Number of patients declaring an increase of psychotropic drug use
|
post-confinement (15 days, 3 months, 6 months)
|
Tobacco consumption
Tijdsspanne: during confinement
|
Number of patients declaring an increase of tobacco consumption
|
during confinement
|
Tobacco consumption
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
Number of patients declaring an increase of tobacco consumption
|
post-confinement (15 days, 3 months, 6 months)
|
alcohol consumption
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
Number of patients declaring an increase of alcohol consumption
|
post-confinement (15 days, 3 months, 6 months)
|
alcohol consumption
Tijdsspanne: confinement
|
Number of patients declaring an increase of alcohol consumption
|
confinement
|
Illicit substances consumption
Tijdsspanne: confinement
|
Number of patients declaring an increase of illicit substances consumption
|
confinement
|
Illicit substances consumption
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
Number of patients declaring an increase of illicit substances consumption
|
post-confinement (15 days, 3 months, 6 months)
|
orientation of life
Tijdsspanne: confinement
|
Life Orinetation Test Revised (LOT-R questionnaire): higher score, more optimistic --> min : 0 max : 24
|
confinement
|
orientation of life
Tijdsspanne: post-confinement (15 days, 3 months, 6 months)
|
Life Orinetation Test Revised (LOT-R questionnaire): higher score, more optimistic --> min : 0 max : 24
|
post-confinement (15 days, 3 months, 6 months)
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Emilie Olie, MD PhD, University Hospital, Montpellier
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- RECHMPL20_0197
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
Klinische onderzoeken op Slef questionnaires fulfilment
-
University Hospital, ToulouseVoltooidAanhoudende pulmonale hypertensie van de pasgeboreneFrankrijk
-
Mỹ Đức HospitalWervingOnvruchtbaarheid | IVF | Ontwikkeling, kind | IVMVietnam
-
Mỹ Đức HospitalVoltooid
-
Mỹ Đức HospitalVoltooid
-
Mỹ Đức HospitalVoltooidOnvruchtbaarheid | IVFVietnam
-
Mỹ Đức HospitalWervingKinder ontwikkeling | Voorbereiding van het endometriumVietnam
-
Mỹ Đức HospitalVoltooidConventionele IVF, ICSIVietnam
-
Mỹ Đức HospitalVoltooid