Clinical Research Recruitment Service

Introducing Our Future Health’s Clinical Research Recruitment Service

Our Clinical Research Recruitment Service enables faster and more efficient recruitment into clinical trials across disease prevention, early detection and treatment.  

We have a cohort of over 2.5 million participants who have consented to be invited to additional research. Researchers can work with us to send targeted invitations to potential participants based on phenotype, genotype, demographics and location.

Our capabilities

We can conduct targeted recruitment to both very large, simple, community-based trials and more challenging studies, such as genetic risk-based recruitment and studies with extensive inclusion/exclusion criteria.

• Prevention and Early-Detection Trials. Our Future Health is uniquely suited for studies in obesity, cardiometabolic disease, mental health and women’s health, where scale, diversity and long follow-up are essential. Use our data to identify sub-cohorts at elevated risk and invite them into behavioural, screening or pharmacological interventions, including vaccines,
• Recall-by-Genotype (RbG) and Polygenic/Integrated Risk Score (PRS) studies. We plan to offer researchers the chance to recruit participants with specific genetic variants or composite risk profiles to validate targets, investigate gene-drug interactions, or test novel diagnostics and therapeutics.
• Recall-by-Phenotype (RbP) studies. Researchers can recruit participants based on biochemical, clinical, or digital phenotypes – such as metabolic markers, diagnoses, or medication – to evaluate diagnostic tools and therapeutics or stratify disease risk.

How we connect researchers with participants

1. Research team approaches Our Future Health with study details. 
2. We undertake a feasibility count to provide estimated number of participants who might be suitable for the study. 
3. We meet the research team to check the study is eligible and discuss the requirements. 
4. If the study is eligible, we ask the researcher to apply to our Access Board for review.  
5. Our Access team provides advice and support with the application. 
6. We develop a targeted invitation strategy and tailored invitations to send to relevant participants, maximising conversion rates. 
7. Invitations are sent to participants subject to further research ethics approvals where required. 
8. We survey and track our participants, their experience and preferences, to improve our service and offering. 

All activity is underpinned by Research Ethics Committee approval, a robust governance and Access Board process, and an unwavering commitment to participant safety, transparency, trust and public benefit.  

Register your interest

Complete the form below to consent to us contacting you about future clinical research recruitment opportunities.

The form is six questions long and asks for information about your work and contact details.

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