Paid research

Paid thalassaemia research studies

MediTalk runs paid healthcare research with patients and caregivers affected by thalassaemia. If you're living with thalassaemia, 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 thalassaemia 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 thalassaemia studies every few weeks. Registered participants hear about them before they go live on the public site.

Register interest

Thalassaemia research , frequently asked questions

Are MediTalk thalassaemia studies paid?

Yes. Every MediTalk research study , including those focused on thalassaemia , 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 thalassaemia research on MediTalk?

Anyone diagnosed with thalassaemia (and in some studies, family members or caregivers of someone with thalassaemia) 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 thalassaemia study work in practice?

Most MediTalk thalassaemia 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 thalassaemia 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 thalassaemia studies right now?

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

Ready to share your thalassaemia 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.