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Evidence

Evidence-based software as medicine

We research continuously, to keep improving a therapy built on the guidelines.

What we measure today

1,500+
patients supported1
84%
still using Noctua Care after one month2
93%
would recommend the program3
4.7
average rating on Google Play4

Guideline alignment

Our therapies build on the accepted guidelines for lowering risk through behavioral and lifestyle therapy.

  • European Society of Cardiology

    The modules follow ESC guidance on secondary prevention: treatment, physical activity, diet, mental health. Every goal the program sets corresponds to a target those guidelines name.

  • Clinical review throughout

    Every module is built with physicians and nursing staff, and reviewed by a cardiologist before it ships.

Our research

What we are working on, and how far along it is.

  • Completed

    Content audit

    Every module in the program reviewed by CHU Bordeaux.

  • Completed

    Behavioral science engine

    Built with the EVIDANS team at CHU Bordeaux.

  • Completed

    DiSuACS engagement trial

    Evaluation of the Feasibility of a Digital Support for Patients after Acute Coronary Syndrome. 32 patients over 30 days. Endpoints: usability and engagement.

  • Q3 2026

    Quantitative analysis

    Behavior change actually implemented after the pilot trial.

  • Q1 2027

    Exploratory randomized trial

    200 patients at CHU de Bordeaux and CH de Pau, evaluating the medical impact of the behavior change program.

Pipeline

Noctua Care can target any cardiometabolic disease, symptom or side effect with an underlying neurological or behavioral component.

  • Coronary artery disease

    Phase 3: Pivotal/Reg

  • Acute coronary syndrome

    Phase 2: Dev/Pilot

  • Peripheral artery disease

    Phase 1: Discovery

  • Atrial fibrillation

    Phase 1: Discovery

  • Heart failure

    Phase 1: Discovery

  1. Patients supported: internal data, August 2026.
  2. Use at one month: DiSuACS, single-arm feasibility study, CHU Bordeaux, 2026. n=32, observed over 30 days. An engagement measure, not an efficacy result.
  3. Recommendation: patient survey, 2026. Sample size and field dates still need recording.
  4. Google Play rating: read from the app listing, August 2026.