Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite
Not a traditional drug phase: "Undetectable & You" HIV treatment literacy app for HIV
Undetectable = Untransmittable (U=U) is the scientific consensus that people with human immunodeficiency virus (HIV) who achieve viral suppression through antiretroviral treatment (ART) cannot transmit the virus sexually. While global studies confirm this, awareness of U=U remains very limited in sub-Saharan Africa, including South Africa, where only two-thirds of people living with HIV (PLHIV) are virally suppressed despite having the largest treatment program globally.
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are "Undetectable & You" HIV treatment literacy app. The registry lists allocation as randomized. Undetectable = Untransmittable (U=U) is the scientific consensus that people with human immunodeficiency virus (HIV) who achieve viral suppression through antiretroviral treatment (ART) cannot transmit the virus sexually.
They plan to enroll about 880 people at Johannesburg. Taking part typically means study visits and measurements plus check-ins.
Official title (unrewritten)
Integrating U=U Into HIV Counseling in South Africa (INTUIT-2.0): a Cluster-Randomized Trial
Interventions: "Undetectable & You" HIV treatment literacy app
Primary outcome (registry wording): HIV viral load <200 copies/mL
Who it is for (from inclusion criteria)
Ages 18 Years to any
Clinic who can join:
Public sector facility
Primary care, outpatient clinic
Follows national guidelines for HIV counseling
Has dedicated HIV counselors
At least 10 patients receiving HIV counseling per week (based on pre-study data)
Follows national guidelines for lab monitoring (CD4 at diagnosis; VLs at 3 and 10 months on ART)
Who the registry excludes
Require acute medical care that would be hindered by participation in the study
Determined by clinical staff not to be physically or emotionally able to initiate ART
Children (under 18 years)
Prisoners or other institutionalized persons
Do not speak one of the primary study languages: English, Zulu, Sotho
Are not able to consent (e.g. intoxicated or of limited mental capacity)
Do not consent to participate in the study, including linkage to clinical records for follow-up
We will investigate the clinical manifestations and molecular genetic defects of heritable urologic malignant disorders. Families with urologic malignancy with known or suspected genetic basis will be enrolled.
This protocol will evaluate patients with systemic lupus erythematosus (SLE) and their relatives to learn more about how the disease develops and changes over time. It will also study genetic factors that make a person susceptible to SLE.
This study is designed to explore the genetics and pathophysiology of diseases presenting with intermittent fever, including familial Mediterranean fever, TRAPS, hyper-IgD syndrome, and related diseases. The following individuals may be eligible for this natural history study: 1) patients with known or suspected familial Mediterranean fever, TRAPS, hyper-IgD syndrome or related disorders; 2) relatives of these patients; 3) healthy, normal volunteers 7 years of age or older.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT07199634?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT07199634?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.