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RecruitingNCT07317687Updated Aug 13, 2026

Rapid HIV, Hep C, and Syphilis Screening in a Rural Street Medicine Clinic

An observational study in HIV Testing, HEPATITIS C (HCV) and Syphilis, sponsored by West Virginia University. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-13.

Sponsored by West Virginia University · Observational

From the registry’s dates

  • Started Jan 2026; still recruiting 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Ages
18 Years and older
Sex
All
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Study summary

West Virginia faces rising rates of HIV, hepatitis, and syphilis, particularly among individuals experiencing homelessness, substance use, and mental health challenges. Traditional blood-draw testing for these infections is often hindered by mistrust, logistical barriers, and delays in results. This study, conducted by the West Virginia University (WVU) Street Medicine program, evaluates a rapid, point-of-care fingerstick test for HIV, Hepatitis C, and syphilis that provides results within 10-20 minutes during mobile clinic visits. Participants may choose rapid testing, traditional blood draw (which also includes Hepatitis B screening), or decline testing. All participants will be invited to complete a brief survey about the experiences with screening methods. The goal is to assess whether rapid testing improves screening uptake, linkage to care, and patient satisfaction, ultimately reducing barriers and disease burden in high-risk populations.

02

Conditions studied

  • HIV Testing
  • HEPATITIS C (HCV)
  • Syphilis
  • Hepatitis B Virus (HBV)

Keywords

  • Street Medicine
  • Rapid Fingerstick Testing
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In context

Hepatitis C

1,743 studies on the registry are indexed under Hepatitis C; 97 are open to participants now.

This study's planned enrollment of 200 is close to the median of 218 across 435 observational studies indexed under Hepatitis C.

Browse Hepatitis C studies →

Lead sponsor

West Virginia University is the lead sponsor of 157 studies on the registry; 36 are open to participants now.

Of its 19 completed or terminated interventional studies of FDA-regulated products, 16 (84%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will include patients in Berkeley and Jefferson Counties of West Virginia who visit the WVU Medicine Street Medicine Clinic.

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

  • Patients of the WVU Medicine Street Medicine team

Exclusion criteria

Exclusion Criteria:

  • Patients under the age of 18
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)
Patient registry
No

Groups and cohorts

  • Participants receiving fingerstick test

    * Will get a quick fingerstick test for HIV, Hepatitis C, and syphilis. * Will receive results in 10-20 minutes. * If positive, will be offered immediate care and/or a referral. * If positive, blood draw will be offered on site to confirm results or referred to a WVU Medicine clinic location for follow-up blood test. * Will be invited to answer survey questions about the feelings and experiences with screening (about 15-30 minutes).

    Diagnostic Test: Rapid Fingerstick Test

  • Participants receiving blood-draw test

    Participants receiving blood-draw test: * Will get a blood draw to test for HIV, Hepatitis B \& C, and syphilis * Will receive results in approximately 3 days (via MyChart message and phone call, or in person at site) * If positive, will be offered immediate care and/or a referral for follow-up care. • Will be invited to answer questions about the feelings and experiences with screening (about 15 minutes).

    Diagnostic Test: Blood Draw for lab test

  • Participants who decline screening

    Participants who decline screening: • Will be invited to answer survey questions about the feelings and experiences with screening (about 15-30 minutes).

Interventions

  • Diagnostic testRapid Fingerstick Test

    Fingerstick test for HIV, Hepatitis B and C, and Syphilis that gives results within 10-20 minutes

  • Diagnostic testBlood Draw for lab test

    Blood draw to test for HIV, Hepatitis B \& C, and syphilis which can take up to 3 days for results

06

What researchers measure

Primary outcomes

  1. Percentage of Finger Stick

    Percentage of participants that opted to take the rapid finger stick test.

    Time frame: Day 1

  2. Percentage of Blood Draw

    Percentage of participants that opted to take the blood draw test.

    Time frame: Day 1

  3. Percentage that decline screening

    Percentage of participants that opted to decline screening

    Time frame: Day 1

07

Study locations

1 of 1 sites recruiting
  • WVU Department of Family Medicine - Eastern Division
    Harpers Ferry, West Virginia 25425, United States
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07317687
Responsible party
Dana Bechtold (Assistant Professor, Department of Family Medicine - Eastern, West Virginia University) — Principal investigator
First posted
Jan 5, 2026
Start date
Jan 21, 2026
Primary completion
Jan 2028 (estimated)
Completion
Jan 2028 (estimated)
Last update
Aug 13, 2026

Study contacts

Dana Bechtold, DO
Contact
dana.bechtold@hsc.wvu.edu
304-535-6343
Dana Bechtold, DO
principal investigator · West Virginia University

Oversight

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

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