Acceptability of Simultaneous Screening for Viral Hepatitis B, C and HIV Among Drug Users in Non-conventional Structures

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Limoges

About this trial

The principle is to propose dedicated monthly screening days bringing together the health personnel involved (hepatologist, addictologist, nurse in charge of the program, addictology nurse and social worker) and to propose appropriate management for each situation assessed.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult 18 and over

Patient frequenting an unconventional structure "outside the walls" or referred by a professional in the care sector

Patient who agreed to participate to the research

Disqualifiers

Patient doesn't agree to participate to the research

Trial population

People followed in unconventional structure care

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Number of RTDs performed compared to the number proposed

Evaluate the acceptability of simultaneous screening for viral hepatitis B, C and HIV among drug users in non-conventional structures using a dual method by RTDs and FibroScan®

Time frame
up to 10 years
2

Number of FibroScan® performed compared to the number proposed

Evaluate the acceptability of simultaneous screening for viral hepatitis B, C and HIV among drug users in non-conventional structures using a dual method by RTDs and FibroScan®

Time frame
up to 10 years

Secondary outcomes

1

Number of days actually completed and the number of participants per session

Evaluate the feasibility of simultaneous screening for viral hepatitis B, C and HIV in drug users in non-conventional structures using a dual screening method TROD and FibroScan®

Time frame
up to 10 years
2

Number and proportion of patients having accepted the immediate consultation with the hepatologist and/or with an addictologist

Evaluate the acceptability of risk reduction methods as part of the care pathway.

Time frame
up to 10 years
3

Number of patients who had social care

Evaluate the impact of screening in terms of patient care.

Time frame
up to 10 years
4

Number of anti-viral B vaccinations offered and carried out

Evaluate the impact of screening in terms of patient care.

Time frame
up to 10 years

Other outcomes

Sponsors and contacts

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