Medically Underserved Area

2

Review clinical trials related to Medically Underserved Area. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

DIALOZIC - Pilot Study of a Diagnostic Pathway for Heart Failure in Rural Areas: the Contribution of Telebiology and Telemedicine

Heart failure is under-diagnosed, even though it is a highly prevalent pathology. The difficulties are accentuated in areas with low medical density. The aim of this project is to demonstrate the value, in terms of diagnosing heart failure, of a Nt-Pro-BNP point of care Test (POCT)in general practices. The aim of this pilot study is to evaluate the reliability of a diagnosis pathway adapted to a low medical density region.

Participants needed: 500
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: University Hospital, MontpellierUpdated: Jul 6, 2026Locations: 1
Eligibility criteria

Patients over 60 years of age [+1]

Patients covered by Articles L1121-5 through L1121-8 of the Public Health Code (... [+2]

Status: Recruiting

Health Ahead Comparative Effectiveness Study

The Health Ahead Comparative Effectiveness Study is a pragmatic, parallel-arm interventional platform that systematically compares successive changes to preventive health screening - each isolated as a single variable against current practice - on the path toward a fully automated screening system deployable in any environment, including the most isolated and resource-limited communities. Each comparison is evaluated with a common set of engagement, behavior-change, experience, cost, and longitudinal outcome measures, allowing results to accumulate on a consistent yardstick across the life of the platform. The first comparison evaluates static versus interactive personalized health report delivery. Subsequent pre-planned comparisons, added by protocol amendment, evaluate mobile community versus fixed laboratory screening; and a hybrid medical-droid plus human-delivery model versus human-only screening. All participants are simultaneously enrolled in the 100-Year Human Aging Study and the Human Observatory Study, contributing individual longitudinal and population-level causal inference data through those protocols.

Participants needed: 1,000,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: William Brandenburg, MDUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+2]