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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02959684
Other study ID # PROunit-STRADA2016
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 14, 2017
Est. completion date July 2019

Study information

Verified date May 2018
Source University Paris 7 - Denis Diderot
Contact Martin Duracinsky, MD, PhD
Phone +33140275543
Email duracinsky.m@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the efficacy of a new screening for infectious diseases: tuberculosis, HIV, HBV and HCV, based on risk factors questionnaires (TB screen for tuberculosis and TROD screen for HIV and hepatitis) amongst a population of legal migrants during their mandatory medical check-up. This study aims for a global improvement of screening and care for migrants.


Description:

In France, the prevalence of infectious diseases such as tuberculosis, HIV/HBV/HCV is high amongst migrants originating from certain countries, hence the official guidelines recommending targeted testing. The rapid testing devices (TROD) give immediate results and reduce missed opportunities. However their use is not yet widespread and migrant populations remain insufficiently tested. Regarding the UNAIDS 90-90-90 goal, France is failing the screening part of the treatment cascade, while 90% of patients are treated and have undetectable viral load. Risk scores based on the best known risk factors for these infections (HIV/HBV/HCV) have previously been developed. They have helped build a pilot of a new unique questionnaire: TROD screen. An electronic survey, called TB screen, was designed to screen for tuberculosis amongst asylum seekers in Switzerland and validated. This survey enables to detect signs of active tuberculosis and may replace the use of pulmonary radiography, thus reducing exposure to X-rays.

It is a prospective multi-centric observational study validating screening tests for HIV/HBV/HCV in two phases:

- Phase 1: a risk score will be validated, including a qualitative study analyzing its acceptability

- Phase 2: its performance will be compared with that of a screening targeted based on the country of origin The phase 1 and phase 2 will include respectively 10.000 and 5000 participants.

For tuberculosis, the efficacy of the improved version of TB screen will be compared with a systematic radiography.

Participation to this study will be voluntary and independent from the delivery of a residence permit. Participants will be informed of it and will systematically receive information about prevention of those infectious diseases.


Recruitment information / eligibility

Status Recruiting
Enrollment 70000
Est. completion date July 2019
Est. primary completion date July 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Migrants undergoing the routine medical visit

- Giving informed consent (oral consent)

Exclusion Criteria:

- Asylum seekers

- Persons not understanding the questionnaire

- Persons aware of their HIV, HBV or HCV positive status

Study Design


Locations

Country Name City State
France OFII Bordeaux Bordeaux
France OFII Cergy Cergy
France OFII Clermont-Ferrand Clermont-Ferrand
France OFII Grenoble Grenoble
France OFII Lille Lille
France OFII Lyon Lyon
France OFII Marseille Marseille
France OFII Melun Melun
France OFII Metz Metz
France OFII Montpellier Montpellier
France OFII Montrouge Montrouge
France OFII Nantes Nantes
France OFII Nice Nice
France OFII Orléans Orléans
France OFII Reims Reims
France OFII Rennes Rennes
France OFII Rouen Rouen
France OFII Toulouse Toulouse

Sponsors (1)

Lead Sponsor Collaborator
University Paris 7 - Denis Diderot

Country where clinical trial is conducted

France, 

References & Publications (6)

Bottero J, Boyd A, Gozlan J, Carrat F, Nau J, Pauti MD, Rougier H, Girard PM, Lacombe K. Simultaneous Human Immunodeficiency Virus-Hepatitis B-Hepatitis C Point-of-Care Tests Improve Outcomes in Linkage-to-Care: Results of a Randomized Control Trial in Persons Without Healthcare Coverage. Open Forum Infect Dis. 2015 Oct 26;2(4):ofv162. doi: 10.1093/ofid/ofv162. eCollection 2015 Dec. — View Citation

d'Almeida KW, Kierzek G, de Truchis P, Le Vu S, Pateron D, Renaud B, Semaille C, Bousquet V, Simon F, Guillemot D, Lert F, Crémieux AC; Emergency Department HIV-Screening Group. Modest public health impact of nontargeted human immunodeficiency virus screening in 29 emergency departments. Arch Intern Med. 2012 Jan 9;172(1):12-20. doi: 10.1001/archinternmed.2011.535. Epub 2011 Oct 24. — View Citation

d'Almeida KW, Pateron D, Kierzek G, Renaud B, Semaille C, de Truchis P, Simon F, Leblanc J, Lert F, Le Vu S, Crémieux AC. Understanding providers' offering and patients' acceptance of HIV screening in emergency departments: a multilevel analysis. ANRS 95008, Paris, France. PLoS One. 2013 Apr 29;8(4):e62686. doi: 10.1371/journal.pone.0062686. Print 2013. — View Citation

Haukoos JS, Lyons MS, Lindsell CJ, Hopkins E, Bender B, Rothman RE, Hsieh YH, Maclaren LA, Thrun MW, Sasson C, Byyny RL. Derivation and validation of the Denver Human Immunodeficiency Virus (HIV) risk score for targeted HIV screening. Am J Epidemiol. 2012 Apr 15;175(8):838-46. doi: 10.1093/aje/kwr389. Epub 2012 Mar 19. — View Citation

Meffre C, Le Strat Y, Delarocque-Astagneau E, Dubois F, Antona D, Lemasson JM, Warszawski J, Steinmetz J, Coste D, Meyer JF, Leiser S, Giordanella JP, Gueguen R, Desenclos JC. Prevalence of hepatitis B and hepatitis C virus infections in France in 2004: social factors are important predictors after adjusting for known risk factors. J Med Virol. 2010 Apr;82(4):546-55. doi: 10.1002/jmv.21734. — View Citation

Schneeberger Geisler S, Helbling P, Zellweger JP, Altpeter ES. Screening for tuberculosis in asylum seekers: comparison of chest radiography with an interview-based system. Int J Tuberc Lung Dis. 2010 Nov;14(11):1388-94. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of the number of HIV, HBV or HCV positive patients identified in both arms of the screening strategy. 2 years
Primary Number of tuberculosis patients identified through the modified TB screen questionnaire 2 years
Secondary Number of HIV/HBV/HCV patients linked to care after being identified through TROD screen. 2 years
Secondary Predictive value of the questionnaire TROD screen. 2 years
Secondary Predictive value of the questionnaire TB screen. 2 years
Secondary Cost-effectiveness of the TROD screen questionnaire compared with a non-targeted screening, calculated in terms of cost per QALY (quality-adjusted life years) gained through this program 2 years
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