Paid research

Paid congenital heart disease research studies

MediTalk runs paid healthcare research with patients and caregivers affected by congenital heart disease. If you're living with congenital heart disease, your perspective shapes the next generation of treatments, devices and patient services , and we pay for your time.

UK GDPR safeCompensated participationNo long applications

No open congenital heart disease studies right now

Register your interest below , we'll email you as soon as one opens.

Get on the list , it's two minutes.

We typically launch new congenital heart disease studies every few weeks. Registered participants hear about them before they go live on the public site.

Register interest

Congenital heart disease research , frequently asked questions

Are MediTalk congenital heart disease studies paid?

Yes. Every MediTalk research study , including those focused on congenital heart disease , offers compensation for your time. Payment varies by study format and length, and is shown on each study's listing before you express interest.

Who can take part in congenital heart disease research on MediTalk?

Anyone diagnosed with congenital heart disease (and in some studies, family members or caregivers of someone with congenital heart disease) can register their interest. Each study has its own eligibility criteria (age, country, treatment history) shown on its listing , so you only spend time on studies you're actually a fit for.

How does a congenital heart disease study work in practice?

Most MediTalk congenital heart disease studies are remote and run on Zoom or a similar video platform , one-to-one interviews, focus groups or online surveys. Time commitment is shown on each listing (typically 30-90 minutes). You only need a quiet space, a webcam and a stable internet connection.

Is my congenital heart disease information kept private?

Yes. MediTalk is a UK-registered healthcare market-research platform run by Medicys Ltd, and all submissions are handled under UK GDPR. Your name and contact details are never shared with study sponsors , only de-identified research insights are reported back.

What if there are no open congenital heart disease studies right now?

Register your interest anyway , registration takes about two minutes, and you'll be the first to hear when a new congenital heart disease study opens. We typically launch new studies every few weeks across many conditions.

Ready to share your congenital heart disease experience?

Two minutes to register. We'll only contact you about studies that match what you've told us , no spam, no third-party sharing.