ClinicalTrials.gg
CompletedNCT05149001RESILSTIGMAUpdated Aug 7, 2026

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

An observational study in HIV Infections, sponsored by University Hospital, Clermont-Ferrand. Completed at 43 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-07.

Sponsored by University Hospital, Clermont-Ferrand · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
667
Ages
18 Years and older
Sex
All
01

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

Read the detailed description

Epidemiological and sociological survey carried out with patients and their caregivers in the CHUs and CHGs of France via the COREVIH from 01/17/2022 to 02/17/2022.

Primary endpoint: Self-stigmatization as experienced by PLWHA will be explored through a patient questionnaire Secondary endpoints:The main explanatory variables will be studied by means of a custom questionnaire intended for the patient and covering psychological flexibility, social provisions, avoidance and fusion mechanisms, quality of life, anxiety and depression.

The socio-demographic explanatory variables will be collected by questionnaire, covering the following areas: sex, age, geographical origin, insecurity, drug use, sexuality, family context, employment, leisure, care environment.

A questionnaire intended for caregivers will study the self-stigmatization perception of the people they care for and the means implemented to fight against self-stigmatization.

Anonymous data will be reported in Redcap. The population will be described by numbers and percentages for categorical variables and by the mean ± standard deviation or the median [interquartile range] for the quantitative variables, with regard to their statistical distribution. Normality will be studied by the Shapiro-Wilk test and / or by histogram. As far as possible, graphical representations will be associated with the analyzes.

02

Conditions studied

  • HIV Infections

Keywords

  • HIV
  • Stigmatization
  • Self-stigma
03

In context

HIV Infections

4,734 studies on the registry are indexed under HIV Infections; 244 are open to participants now.

This study's enrollment of 667 is above the median of 200 across 781 observational studies indexed under HIV Infections.

Browse HIV Infections studies →

Lead sponsor

University Hospital, Clermont-Ferrand is the lead sponsor of 859 studies on the registry; 179 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

people living with HIV

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • For patients: adult patient, male or female, infected with medically monitored in a hospital department involved in the investigation.
  • Affiliation to a Social Security scheme For caregivers:Caregiver caring for people living with HIV as part of a hospital service involved in the survey (doctor, IDE, psychologist, other ...).

Exclusion criteria

Exclusion Criteria:

  • Minor patient
  • Refusal of participation
  • Persons under guardianship, guardianship or legal protection
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
667 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Self-stigma as experienced by PLHIV will be explored through a custom questionnaire intended for the patient

    Percentage of patient with self-stigma

    Time frame: 1 day during the scheduled consultation in the infectious diseases department of the Gabriel Montpied University Hospital in Clermont-Ferrand

Secondary outcomes

  1. The main explanatory variables will be studied by means of a custom questionnaire intended for the patient

    multivariate analysis of factors associated with disparition of self-stigma

    Time frame: 1 day during the scheduled consultation in the infectious diseases department of the Gabriel Montpied University Hospital in Clermont-Ferrand

  2. Self-stigma of patients perceived by their caregivers

    Percentage of caregivers who perceive self-stigma and how they propose to their patients the way to surpass themselves

    Time frame: 1 day during the scheduled consultation in the infectious diseases department of the Gabriel Montpied University Hospital in Clermont-Ferrand

07

Study locations

43 sites
  • Centre Hospitalier du Pays d'Aix
    Aix-en-Provence, France
  • Chu Angers
    Angers, France
  • CH Annecy Genevois
    Annecy, France
  • Chru Besancon
    Besançon, France
  • CHRU Brest
    Brest, France
  • CH Cholet
    Cholet, France
  • Hopital Antoine Beclere
    Clamart, France
  • Clermont-Ferrand University Hospital
    Clermont-Ferrand, France
  • Chu Dijon
    Dijon, France
  • Hopital Raymond Poincaré
    Garches, France
  • CHD Vendrée
    La Roche-sur-Yon, France
  • Groupe Hospitalier de La rochelle-Ré-Aunis
    La Rochelle, France
  • CH de Versailles
    Le Chesnay, France
  • Hopital Bicetre Aphp
    Le Kremlin-Bicêtre, France
  • Ch Le Mans
    Le Mans, France
  • Centre Hospitalier Bretagne Sud
    Lorient, France
  • CHU LYON
    Lyon, France
  • CISIH
    Marseille, France
  • Ch Montlucon
    Montluçon, France
  • CH Morlaix
    Morlaix, France
  • CH Moulins-Yzeure
    Moulins, France
  • CHU de Mulhouse
    Mulhouse, France
  • Chu Nantes
    Nantes, France
  • CHU NICE
    Nice, France
  • CH NIORT
    Niort, France
  • CH Orléans
    Orléans, France
  • Hopitel Necker
    Paris, France
  • CH Perpignan
    Perpignan, France
  • Chu Poissy
    Poissy, France
  • CHU Poitiers
    Poitiers, France
  • Centre Hospitalier Intercommunal de Cornouaille
    Quimper, France
  • Pole Santé Publique - CH Laennec
    Quimper, France
  • Chu Reims
    Reims, France
  • CHU Nord
    Saint-Etienne, France
  • CHU Strasbourg
    Strasbourg, France
  • Hopital Tenon
    Thenon, France
  • Chu Toulon
    Toulon, France
  • Ch Valenciennes
    Valenciennes, France
  • CHBA Vannes
    Vannes, France
  • CH VICHY
    Vichy, France
  • Hôpital Nord Ouest villefranche sur Saone
    Villefranche-sur-Saône, France
  • CHU Pointe-à-Pitre
    Pointe-à-Pitre, Guadeloupe
  • CHU Felix Guyon
    Saint-Denis, Reunion
08

References and documents

Publications

  • Jacomet C, Miele C, Goncalves E, Lambert C, Belletier C, Linard F, Phalip-Le Besnerais J, Dellamonica P, Dambrun M. RESILSTIGMA. Resilience to self-stigmatization experienced by people living with HIV: Which self-reported factors improve awareness among health workers? PLoS One. 2025 Feb 6;20(2):e0311776. doi: 10.1371/journal.pone.0311776. eCollection 2025. PubMed 39913414 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jan 2022 to primary completion in Apr 2022, 2 months.

Of 187 non-industry observational studies under HIV Infections, half reached primary completion within 37 months of starting (the median), counting those still running; a quarter within 16 and three quarters within 69. This study's 2 months is below that.

Counting every sponsor, half of 201 studies reached it within 38 months; a quarter within 16 and three quarters within 69.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 29, 2021
First posted
Dec 8, 2021
StartActual
Jan 17, 2022
Primary completionActual
Apr 14, 2022
CompletionActual
Apr 14, 2022
Last update
Aug 7, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05149001
Collaborators
Poitiers University Hospital, Poissy-Saint Germain Hospital, Centre Hospitalier Universitaire Dijon, Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer, Hopital Antoine Beclere, Nantes University Hospital, Hospital, La Roche sur Yon, Hôpital Necker-Enfants Malades, Centre Hospitalier de Bretagne Sud, Reims University hospital, Groupe Hospitalier de la Rochelle Ré Aunis, Hospital Laennec, Quimper, University Hospital, Brest, Hospital Cornouaille, Quimper, Centre Hospitalier de Cholet, University Hospital, Strasbourg, CH Annecy Genevois, Perpignan Hospital Center, Centre Hospitalier le Mans, Centre Hospitalier VALENCIENNES, Bicetre Hospital, Centre Hospitalier Universitaire de Nice, University Hospital, Marseille, Jacques Lacarin Hospital Center, L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône, Centre Hospitalier Universitaire de Besancon, Hospital, Vannes, Moulins Hospital, Hospital, Montluçon, Centre Hospitalier de Niort, Hôpital Edouard Herriot, Hospital La Source, Orléans, Centre Hospitalier du Pays d'Aix, Hospital Andre Mignot, Le Chesnay, Hôpital Raymond Poincaré, University Hospital, Angers, University Hospital, Pointe-à-Pitre, Centre Hospitalier des Pays de Morlaix, Hospital Foch, Suresnes, Tenon Hospital, Paris, University Hospital of Saint-Etienne, Centre Hospitalier de Saint-Denis, University Hospital, Mulhouse
Responsible party
Sponsor
First posted
Dec 8, 2021
Start date
Jan 17, 2022
Primary completion
Apr 14, 2022
Completion
Apr 14, 2022
Last update
Aug 7, 2026

Study contacts

Christine JACOMET, Dr
principal investigator · University Hospital, Clermont-Ferrand

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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