Study Among People Living With HIV and Their Health Professionals of Associated Factors of Resilience to Self-stigma

NCT05149001 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 667

Last updated 2023-05-01

No results posted yet for this study

Summary

This study is perform to study the effect of psychological and psychosocial factors associated with resilience to the self-stigmatization of people living with HIV

Conditions

  • HIV Infections

Sponsors & Collaborators

  • Poitiers University Hospital

    collaborator OTHER
  • Poissy-Saint Germain Hospital

    collaborator OTHER
  • Centre Hospitalier Universitaire Dijon

    collaborator OTHER
  • Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

    collaborator OTHER
  • Hopital Antoine Beclere

    collaborator OTHER
  • Nantes University Hospital

    collaborator OTHER
  • Hospital, La Roche sur Yon

    collaborator UNKNOWN
  • Hôpital Necker-Enfants Malades

    collaborator OTHER
  • Centre Hospitalier de Bretagne Sud

    collaborator OTHER
  • Reims University hospital

    collaborator OTHER
  • Groupe Hospitalier de la Rochelle Ré Aunis

    collaborator OTHER
  • Hospital Laennec, Quimper

    collaborator UNKNOWN
  • University Hospital, Brest

    collaborator OTHER
  • Hospital Cornouaille, Quimper

    collaborator UNKNOWN
  • Centre Hospitalier de Cholet

    collaborator OTHER
  • University Hospital, Strasbourg

    collaborator OTHER
  • CH Annecy Genevois

    collaborator OTHER
  • Centre hospitalier de Perpignan

    collaborator OTHER
  • Centre Hospitalier le Mans

    collaborator OTHER
  • Centre Hospitalier VALENCIENNES

    collaborator OTHER
  • Bicetre Hospital

    collaborator OTHER
  • Centre Hospitalier Universitaire de Nice

    collaborator OTHER
  • University Hospital, Marseille

    collaborator OTHER
  • Jacques Lacarin Hospital Center

    collaborator OTHER
  • L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône

    collaborator OTHER
  • Centre Hospitalier Universitaire de Besancon

    collaborator OTHER
  • Hospital, Vannes

    collaborator UNKNOWN
  • Moulins Hospital

    collaborator OTHER
  • Hospital, Montluçon

    collaborator UNKNOWN
  • Centre Hospitalier de Niort

    collaborator OTHER
  • Hôpital Edouard Herriot

    collaborator OTHER
  • Hospital La Source, Orléans

    collaborator UNKNOWN
  • Centre Hospitalier du Pays d'Aix

    collaborator OTHER
  • Hospital Andre Mignot, Le Chesnay

    collaborator UNKNOWN
  • Hôpital Raymond Poincaré

    collaborator OTHER
  • University Hospital, Angers

    collaborator OTHER_GOV
  • University Hospital, Pointe-à-Pitre

    collaborator UNKNOWN
  • Centre Hospitalier des Pays de Morlaix

    collaborator OTHER
  • Hospital Foch, Suresnes

    collaborator UNKNOWN
  • Tenon Hospital, Paris

    collaborator OTHER
  • University Hospital of Saint-Etienne

    collaborator OTHER
  • Centre Hospitalier de Saint-Denis

    collaborator OTHER
  • University Hospital, Mulhouse

    collaborator UNKNOWN
  • University Hospital, Clermont-Ferrand

    lead OTHER

Principal Investigators

  • Christine JACOMET, Dr · University Hospital, Clermont-Ferrand

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-17
Primary Completion
2022-04-14
Completion
2022-04-14

Countries

  • France
  • Guadeloupe
  • Reunion

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05149001 on ClinicalTrials.gov