Protocol RV 583 Multinational Observational Cohort of HIV and Other Infections

HIV Infections Clinical Trial

— MOCHI  

Official title:

Multinational Observational Cohort of HIV and Other Infections (MOCHI)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05147519
• Other study ID #: RV 583
• Secondary ID: WRAIR # 2877b
• Status: Recruiting
• Start date: November 5, 2021
• Est. completion date: June 30, 2032

Study information

• Verified date: April 2023
• Source: Henry M. Jackson Foundation for the Advancement of Military Medicine
• Contact: Trevor A. Crowell, MD, PhD
• Phone: 301-500-3990
• Email: tcrowell[@]hivresearch.org
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Multinational Observational Cohort of HIV and other Infections (MOCHI). This observational study is to gain information regarding the number of new HIV infections among people who engage in behaviors that make them vulnerable to acquiring HIV across multiple international sites.

Description:

The study will be a multi-site prospective observational cohort of males and females who are vulnerable to HIV and other STIs. Step 1 of the study is the evaluation of participants without HIV with quarterly follow up visits up to 72 weeks. At each follow up visit, we will administer behavioral questionnaires, HIV testing, STI testing, and other laboratory testing per the schedule of evaluations. Participants will also perform home-based HIV testing between study visits per the schedule of evaluations. Step 2 is the incident HIV acquisition evaluation. Follow-up visits will be conducted every four weeks up to 12 weeks after initial HIV diagnosis and then quarterly up to 48 weeks. Individuals will be monitored for HIV disease outcomes, STIs, and surveys, and other lab collections will be administered per the schedule of evaluations. Participants who are virally-suppressed at the completion of Step 2 will transition to Step 3 for long-term follow-up semi-annually out to week 192. Evaluation will primarily be HIV monitoring, surveys for consideration of trial participation, and specimen storage per the schedule of evaluations.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 2500
• Est. completion date: June 30, 2032
• Est. primary completion date: June 30, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 15 Years to 55 Years

Eligibility

Step 1 Inclusion Criteria:

• Female or male aged 15-55 years
• Documented negative HIV test according to site-specific HIV testing procedures at entry/screening
• Able and willing to provide informed consent
• Willing to provide biometric identification
• Available for follow-up for the planned study duration
• Understands English or the local language as approved by the IRB, including people who are illiterate
• Willing to provide contact information for themselves and one personal contact who would know their whereabouts during the study period
• Willing to provide information regarding HIV risk behaviors and to undergo testing for HIV and other STIs
• Considered to be vulnerable to HIV and other STIs based on any one or more of the

following test results and/or self-reported behaviors:

1. Documented history of newly diagnosed syphilis, gonorrhea, chlamydia, Mycoplasma genitalium, herpes simplex virus, or acute hepatitis C virus infection in the 24 weeks prior to screening

2. Self-reported vaginal, oral, or anal intercourse in exchange for money as a regular source of income

3. Self-reported condomless vaginal or anal intercourse with at least three different partners living with HIV or of unknown status in the 24 weeks prior to screening

4. Self- reported injection drug use (IDU) in the 24 weeks prior to screening

5. Self-reported insertive or receptive anal or neovaginal intercourse with one or more different male or transgender partners in the 24 weeks prior to screening Step 2 Inclusion Criteria

• New diagnosis of HIV in the last 90 days during Step 1 as determined by site-specific HIV testing procedures
• Able and willing to continue follow-up for the planned study duration Step 3 Inclusion Criteria
• Virally-suppressed at the completion of Step 2
• Adherent to ART
• Able and willing to continue follow-up for the planned study duration Step 1 Exclusion Criteria
• Any significant condition (medical, psychologic/psychiatric or social) that, in the judgment of the study investigator, might interfere with the conduct of the study
• Active drug or alcohol use or dependence that, in the judgement of the study investigator, would interfere with adherence to study requirements
• Current or past participation in a preventive or therapeutic HIV vaccine study, unless known placebo recipient
• Positive ß-HCG (human chorionic gonadotropin) pregnancy test (urine or serum) at screening for people of child-bearing potential and people who are amenorrheic for less than 12 consecutive months. Step 2 Exclusion Criteria
• Any significant condition (medical, psychologic/psychiatric or social) that, in the judgment of the study investigator, might interfere with the conduct of the study
• Active drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements Step 3 Exclusion Criteria
• Any significant condition (medical, psychologic/psychiatric or social) that, in the judgment of the study investigator, might interfere with the conduct of the study
• Active drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements

Related Conditions & MeSH terms

• Communicable Diseases
• HIV Infections
• Infections

Intervention

Behavioral:
• Novel interventions to achieve HIV remission
To establish a group of well-characterized people living with HIV who initiated ART during acute or early HIV transmission that can serve as a source population for future studies, including those designed to test novel interventions to achieve HIV remission.

Locations

Country	Name	City	State
Kenya	Kenya Medical Research Institute/ USAMRD-A/Kenya (Kericho)	Kericho
Uganda	Makerere University Walter Reed Program	Makerere	Kampala

Sponsors (1)

Lead Sponsor	Collaborator
Henry M. Jackson Foundation for the Advancement of Military Medicine

Countries where clinical trial is conducted

Kenya,  Uganda, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Establish HIV Incidence at All Sites	For the analysis of the incidence rate, only individuals who are not living with HIV at the baseline exam will be included in the incidence rate analysis.; People without HIV will contribute person-time beginning with the time they enter the study until the study concludes or they are either censored or an HIV transmission event occurs. The event time for each subject is set to the minimum of the HIV transmission event time or the censoring time caused by one of the following: a drop-out event, a death event, or study end event. If one of these censoring events occurs, the censoring time is set to the last time there is recorded data for the subject. If an individual tests positive for HIV during the study, the HIV transmission event time is set to the visit during which the HIV transmission occurred. Those individuals who are lost to follow-up after enrollment will be censored at the last visit.	10 Years
Secondary	Establish Incidence and Prevalence of STIs Including Chlamydia, Gonorrhea, Syphilis, and Mycoplasma genitalium	For incident cases, the date of the positive test will be used as the date of infection. Specifically, for syphilis, a positive test can be determined by one of the following algorithms: 1. In the traditional algorithm, a non-treponemal test (e.g., rapid plasma reagin [RPR] or Venereal Disease Research Laboratory test [VDRL]) is used as the initial screen and reactive samples are confirmed with a treponemal test (e.g., fluorescent treponemal antibody absorption [FTA-ABS], T. pallidum particle agglutination [TPPA] test, Treponema pallidum particle agglutination assay [TPHA], or Syphilis IgG) or other tests that detect targets specific to T. pallidum. 2. The reverse algorithm uses a treponemal test for screening with reactive samples followed up with a non-treponemal test.	10 Years
Secondary	Willingness to Participate and Other Calculations	Willingness to participate in an HIV vaccine trial and study retention rates and their respective 95% CIs will be estimated assuming a binomial distribution. Factors associated with willingness to participate in vaccine trial will be evaluated using logistic regression models. Self-reported risk behavior over time will be assessed by frequency tables and bar graphs. Changes in risk behavior over time will be evaluated using a Generalized Estimating Equation (GEE) model with clustering occurring within individuals (ex: multiple observations per person). Knowledge, attitudes, and practices regarding behaviors and preventive measures will be evaluated using descriptive statistics.	10 Years