Projects

REFLEX

This three-year multi-site NHS research study (2023–2026) evaluated the clinical and cost-effectiveness of screening methods to identify individuals at high risk for hepatocellular carcinoma (liver cancer) and metabolic-associated fatty liver disease.

As the project lead, I managed the lifecycle from initial research feasibility and evidence gap analysis through to study development, NHS setup, recruitment, data collection, analysis, and publication.

Key Metrics:

Randomised controlled trial (RCT)

26 active NHS sites

640 participants recruited

End-to-End Deliverables:

Research Question Protocol Patient Materials Costing Funding Secured PPIE Study Website IRAS & Ethics Site & Participant Recruitment Data Collection & Database Analysis Publication

Liver Service

NHS-commissioned community diagnostic service.

I established and led the Southampton Community Liver Assessment Service embedded within primary care, providing FibroScan assessments for GP-referred. Alongside clinical delivery I evaluated routine patient data to publish a formal service evaluation and develop the ALBA algorithm for targeted liver disease identification.

Key Metrics:

Scaled from Southampton to South West Hampshire GP practices

Maximised secondary care efficiency via timely, high risk referrals

Reduced unnecessary hospital referrals through local triage

End-to-End Deliverables:

Clinical Pathway Co-design Primary Care Embedding FibroScan Service Delivery Lifestyle Advice Integration GP Trust & Engagement PPIE Data Analysis ALBA Algorithm Development Site & Participant Recruitment Published Service Evaluation Regional expansion

ESCALATE

Effectiveness evaluation embedded within a new NHS service.

I am leading the academic evaluation of a new NHS service delivering Endoscopic Sleeve Gastroplasty (ESG) for patients with compensated advanced chronic liver disease secondary to metabolic associated-dysfunction steatotic liver disease (MASLD). This will be a mixed methods feasibility study to establish routine clinical acceptability and generate the foundational data needed for a future multi-centre randomised controlled trial (RCT).

Key Metrics:

Funding applied for to run this innovative pilot evaluation

Implemented updated global MASLD diagnostic criteria

Direct pipeline to future multi-centre national RCT

End-to-End Deliverables:

Academic Evaluation Design Funding Secured Protocol Development Study Sponsor Review IRAS & Ethics Submission Service Integration Mixed Methods Data Collection Feasibility Analysis

LOCATE

Qualitative and Longitudinal Evaluation.

While serving as Trial Manager for the LOCATE study (evaluating GP-embedded liver nurse support), I identified a gap for a qualitative process evaluation. Operating through Core Minutes Research, I independently designed and executed this study to map the implementation barriers and facilitators within primary care. Recognising a further evidence gap, I subsequently designed, funded, and led a 54-month post-recruitment longitudinal follow-up study—repeating baseline assessments and rescanning participants—to evaluate long-term outcomes.

Key Metrics:

Transitioned from Trial Manager to Independent Lead Investigator

Secured Indepdent funding for both sub-studies

Delivered long-term longitudinal data (54 months post-recruitment)

Published two distinct peer-reviewed papers as lead investigator

End-to-End Deliverables

Opportunity Identification Protocol Development Regulatory Approvals Fieldwork & Qualitative Analysis First Publication Long-term Funding Secured Follow-up Protocol Longitudinal Patient Rescanning Second Publication

PIVOT

Overcoming geographical inequalities in liver care

I designed the development of the PIVOT study, a mixed-methods natural experimental evaluation of an integrated, mobile community liver assessment service for patients with type 2 diabetes. Having completely finalised the design, protocol, patient literature, and formal NHS Sponsor approval, the project is fully “shovel-ready” and currently positioned for funding acquisition.

Key Metrics:

Researcher-led natural experimental design

Completed governance pipeline ready for immediate rollout

Targeted primary care intervention for high-risk diabetes pathways

End-to-End Deliverables:

Concept & Design Protocol Finalised Patient Information Developed IRAS Submission Prepared Sponsor Approval Secured Funding Acquisition (current) Launch Mixed-Methods Evaluation