PSY-COEHPAD-OC: Post-traumatic Stress, Signs of Depression and Burnout Syndrome Among Nursing Home Staff in Occitanie During the COVID-19 Pandemic

Sponsor
Centre Hospitalier Universitaire de Nīmes (Other)
Overall Status
Completed
CT.gov ID
NCT04916275
Collaborator
(none)
501
3
3.2
167
52.9

Study Details

Study Description

Brief Summary

Nursing home staff face multiple stresses during the Covid-19 pandemic including personal risk of infection, risk of transmission of the virus to residents and relatives, and risk of witnessing end-of-life scenarios under difficult contexts (absence of families). The hypothesis of this study is that the Covid-19 period is associated with an incidence of more than 30% of post-traumatic stress in nursing home staff.

Condition or Disease Intervention/Treatment Phase
  • Other: Cognitive tests

Study Design

Study Type:
Observational
Actual Enrollment :
501 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Stress Post Traumatique, Signes de dépression et Syndrome d'épuisement Professionnel Chez le Personnel Des EHPAD en Occitanie Pendant la pandémie COVID-19 : étude Prospective
Actual Study Start Date :
May 27, 2021
Actual Primary Completion Date :
Aug 31, 2021
Actual Study Completion Date :
Aug 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Staff working in a nursing home in Occitanie

Other: Cognitive tests
Optional tests: Corsi block-tapping task, Stroop test and Iowa gambling task

Outcome Measures

Primary Outcome Measures

  1. To assess the prevalence of post-traumatic stress disorder (PTSD) in the context of the COVID-19 health crisis [Day 0]

    Posttraumatic Stress Disorder Checklist Scale (PCL-5) scale, where the recommended cut-off threshold for screening is 44

Secondary Outcome Measures

  1. Prevalence of depression in the context of the COVID-19 health crisis [Day 0]

    Hospital Anxiety and Depression Scale (HADS) scale, using a cut-off above 7

  2. Prevalence of burn out in the context of the COVID-19 health crisis [Day 0]

    Masslach Burn out Inventory (MBI) questionnaire where high scores for the professional burnout and depersonalization sections and a low score for the personal accomplishments section will signal burn out

Other Outcome Measures

  1. Optional assessment of work memory abnormalities associated with symptoms of post-traumatic stress disorder, anxiety and depression [Day 0]

    Corsi block-tapping task - score ranging from 0(good memory) -18(bad memory)

  2. Optional assessment of cognitive flexibility abnormalities associated with symptoms of post-traumatic stress disorder, anxiety and depression [Day 0]

    Corsi block-tapping task - score ranging from 0(good memory) -18(bad memory)

  3. Optional assessment of decision-making abnormalities associated with symptoms of post-traumatic stress disorder, anxiety and depression [Day 0]

    Iowa Gambling Task - score ranes from -14 to +40

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Professional working in a nursing home in Occitanie

  • Professional agreeing to participate

  • Professional in a nursing home for at least 3 months

  • Professional able to read French

  • Profession with an internet connection

Exclusion Criteria:
  • The subject is in a period of exclusion determined by a previous study

  • The subject refuses to participate

  • The subject has already been included into the study

  • It is impossible to give the subject informed information

  • The subject is under safeguard of justice or state guardianship

  • The subject is unable to express consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU de Montpellier Montpellier France
2 CHU de Nîmes, Hôpital Universitaire Carémeau Nimes France 30029
3 CHU de Toulouse Toulouse France

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nīmes

Investigators

  • Principal Investigator: Ismaël Conejero, CHU de Nimes

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier:
NCT04916275
Other Study ID Numbers:
  • Local/2020/COVID/JYL IC-04
First Posted:
Jun 7, 2021
Last Update Posted:
Oct 4, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 4, 2021