EMPOWER-1: A Multi-site Clinical Cohort Research Study to Reduce Health Inequality

Last updated: March 5, 2025
Sponsor: Future Genetics Limited
Overall Status: Active - Recruiting

Phase

N/A

Condition

Arthritis And Arthritic Pain

Peripheral Arterial Occlusive Disease

Diabetes And Hypertension

Treatment

N/A

Clinical Study ID

NCT03987633
EMPOWER-1
  • Ages > 6
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Health inequality and genetic disparity are a significant issue in the United Kingdom (UK).

This study focuses on diseases that are associated with significant morbidity and mortality in the UK, and specifically examines the extent and basis of treatment failure in different patient populations.

The vast majority of drug registration clinical trials have under-representation of ethnic minority populations. In addition, the wider Caucasian populations have reasonably different clinical characteristics to the population that participated in the drug licencing clinical trials. A consequence of this is that drugs are licensed for use in real-world general patient populations where the clinical trial results are simply not statistically significant to specifically demonstrate efficacy or safety in populations that were either absent or under-represented in the drug registration clinical trials. When these facts are considered alongside data that supports significant under-reporting of adverse events in the real-world setting within the UK (and globally, e.g the USA and Europe), it highlights that pharmacovigilance systems are unable to capture drug effectiveness and safety data in a manner that can reasonably assure appropriate prescribing in the wider patient populations.

This large real-world research study aims to identify whether commonly prescribed drugs are effective in treating illnesses that cause significant poor health and death in the different patient populations that represent the UK.

The goal of this study is to generate large quantitative data-sets that may inform clinical practice to reduce the existing health inequality and genetic disparity in the UK.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patients or their relative/family member is diagnosed with the illness beinginvestigated by this study.

  2. All NHS patients that are associated with a participating study site, but do notfall under the first bullet point above, may participate with a view that they maypotentially contribute to a case control population in the research study.

  3. Subjects agree to:

  4. Gift biological samples, i.e. saliva. Where practical, blood or otherbiological samples may be voluntarily provided by the patient.

  5. Provide Consent for access to medical records.

  6. Complete disease specific, quality of life, and study associatedquestionnaires.

Exclusion

Exclusion Criteria:

  1. Patient does not provide a valid consent for study participation.

  2. Patient is not registered with the NHS for care.

  3. Patient lacking capacity, who does not have an illness that is being specificallyinvestigated by this clinical research study.

  4. Person lacks capacity and where the personal consultee has not advised that thePerson may enrol, in accordance with the Mental Health Act 2005.

Study Design

Total Participants: 200000
Study Start date:
February 01, 2020
Estimated Completion Date:
February 01, 2030

Study Description

This multi-centre real-world study will recruit patients across different National Health Service (NHS) sites based in England, where the overall patient population demographic profile is sufficiently variable to allow for meaningful representation of different ethnicities in the analysis of pooled data-sets.

The study addresses the issue of health inequality and genetic disparity in the United Kingdom (UK) by recruiting up to 200,000 patients primarily from the three main ethnic groups in the UK; namely White (Caucasian), African-Caribbean (Black), and South Asian (Asian) populations on a 1:1:1 ratio.

Biological samples, medical records, alongside specific questionnaires will be used in data analyses to help identify treatment failures in different populations for the 19 disease areas under investigation, which are a significant cause of morbidity and mortality in the UK.

Analysis of patient populations may provide real-world evidence around disease prevalence between and within different ethnic groups. The data may also support hypothesis driven genetic analysis to identify putative bio-markers associated with treatment failure.

Data from this study will be published, and findings could better inform clinical practice in the management of diseases that cause significant poor health and death in the different populations that represent the UK.

Connect with a study center

  • Future Genetics Limited

    Birmingham, West Midlands B15 2SQ
    United Kingdom

    Site Not Available

  • Future Genetics, The Science Centre, Wolverhampton Science Park

    Wolverhampton, West Midlands WV10 9RU
    United Kingdom

    Active - Recruiting

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