RecruitingNCT06641726

Creating a Global Research Database That Connects Genetic Information and Long-term Health Data to Improve Personalized Treatment for People With Serious Mental Illness

Developing an Internationally-diverse, Linked Genomic and Longitudinal Phenotypic Research Dataset to Accelerate Precision Psychiatry for Patients With Serious Mental Illness


Sponsor

Akrivia Health

Enrollment

50,000 participants

Start Date

May 16, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

This observational study aims to provide new insights into the nature and classification of severe mental illness and dementias that in time should help improve diagnostic practise, and enable the development of new and improved treatments. The investigators will achieve aims by gathering information and biological samples from over 50,000 research participants and then linking this information with participants' electronic health records, genetic and other potential markers of mental illnesses (called biomarkers, derived from biological samples). The investigators will use this resource to analyse how potential risk factors - genetic, other biological and non-biological (related to the participants' life circumstances) - influence participants' experiences, symptoms, and outcomes (both mental and physical health). The investigators will also use advanced analysis to assess whether there may be better ways of grouping together and understanding the experiences of those with severe mental illnesses and dementias. Given the value and importance of this resource for advancing mental health research, the investigators will also make the data available to other researchers to pursue these broad research aims.


Eligibility

Min Age: 18 YearsMax Age: 110 Years

Plain Language Summary

Simplified for easier understanding

This study is building a global research database that links genetic information with long-term health records to improve personalized treatment for people with serious mental illness or dementia. **You may be eligible if...** - You are 18 years or older - You have an electronic health record in a primary or secondary care service - You have been diagnosed with or treated for depression, bipolar disorder, schizophrenia, dementia, or mild cognitive impairment — OR you have been referred to a memory clinic - You can speak English - You are able and willing to complete a cognitive assessment (if applicable) **You may NOT be eligible if...** - You lack the capacity to provide consent - You cannot understand spoken or written English (for the dementia group) - You have an intellectual disability - You have certain specific types of dementia (e.g., related to Huntington's disease, HIV, or alcohol) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERNot applicable- observational study

This is non-interventional, cross-sectional observational study and thus there is no intervention.


Locations(1)

GlobalMinds central study team

Oxford, Oxford, United Kingdom

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NCT06641726


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