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Evidence

Evidence-based software as medicine

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

Used most days, well beyond the first month

How often do patients use Noctua Care?

1,500+
patients supported1
84%
use Noctua Care beyond one month2
5+
days of use per week, on average2
93%
recommend Noctua Care to other patients3
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.

Studies and development status

What is Noctua Care studying next?

  • 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. 30 patients over 30 days. Endpoints: usability and engagement. Health Data Hub registration 30001700.

  • 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. Usage: DiSuACS, Health Data Hub registration 30001700, single-arm feasibility study, CHU Bordeaux, 2026. n=30, observed over 30 days.
  3. Recommendation: patient survey, 2026.
  4. Google Play rating: read from the app listing, August 2026.