Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsN/A

IONA Longitudinal Cohort Study

Sponsor: Brain Health Scotland Life Sciences Ltd

NCT ID: NCT05892952

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 120 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
50 Years to 120 Years
Who
All
Number of participants
10,000
Started
2023-12-21
Last checked
2025-09

Plain English Summary

What is this study?

  • • Testing a new treatment for alzheimer disease
  • • Clinical study - 10,000 participants
  • • Understanding more about how diseases that cause dementia develop is critical as the number of people living with, or affected by, dementia in Scotland continues to grow

Who can take part?

  • • Ages 50 Years to 120 Years
  • • Diagnosed with alzheimer disease

Where?

  • • Edinburgh - Scottish Brain Sciences Arran Facility

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Understanding more about how diseases that cause dementia develop is critical as the number of people living with, or affected by, dementia in Scotland continues to grow. The IONA Longitudinal Cohort Study (LCS) has been set up to gather information about people's cognitive health (their memory and thinking abilities), their lifestyle and health risk factors for future dementia (such as hearing loss and obesity), genetics and disease biomarkers, over a number of years. The IONA LCS has three main objectives: Firstly to develop this cohort that is well characterised (also known as being "well-phenotyped") that represent the Scottish population (taking into consideration age, sex, ethnicity and education). The second objective is to use this data to build disease models to better understand trajectories of diseases, and identify any sub-populations who have different (i.e. better, worse) disease trajectories. Finally the third objective for IONA LCS is to offer people an optional consent to hear about future studies they may be interested in taking part in.

More detail

IThe IONA Longitudinal Cohort Study (LCS) will provide a well-phenotyped (combining data on risk factors for dementia, cognitive assessment results, disease biomarkers and genetics) population representative of the Scottish population aged 50 and above across the spectrum of risk for, and the earliest disease stages of, AD dementia and other neurodegenerative conditions. Recent therapeutic successes in the treatment of Mild Cognitive Impairment (MCI) due to Alzheimer's disease (AD) and mild AD, as well as progressions in diagnostic tools such as blood-based biomarkers, has energised the field to develop more specific diagnostics and therapies following the best principles of precision medicine. Large, 'real world' cohorts are needed to understand whether these, and other future breakthroughs, are valid in real world populations away from highly selective clinical trials. Precision medicine requires identification of disease sub-populations who share similar diagnostic profiles that reflect similar disease mechanisms and hence are likely to respond consistently to specific therapeutic interventions. This will require detailed clinical, genetic and biological phenotyping. IONA LCS will recruit uniquely in Scotland and will ensure that a large, diverse, real-world population will be available to drive developments globally of more accurate diagnostics and accelerate the development of new disease modifying therapies.

Alzheimer DiseaseDementia

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 50 Years - 120 Years
  • Who can join: All genders

What the study is looking for

  • ✓Age at least 50 years.
  • ✓Living in Scotland.
  • ✓Able to read and write and with minimum 7 years of formal education.
  • ✓Have a study partner who is aged 18 years or older.
  • ✓Have capacity to provide agreement to take part at baseline.
See the full criteria
* Age at least 50 years. * Living in Scotland. * Able to read and write and with minimum 7 years of formal education. * Have a study partner who is aged 18 years or older. * Have capacity to provide informed consent at baseline. * Able to speak English to a level where the cognitive assessments can be completed.

Where Is This Study? (1 UK site)

Scottish Brain Sciences Arran Facility

Edinburgh EH12 9DQ, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Sarah Gregory, PhD

Sponsor contact

CONTACT

0131 353 0233 s.gregory@brainsciences.scot

Joseph Milne

Sponsor contact

CONTACT

j.milne@brainsciences.scot
Data sourced from ClinicalTrials.gov · Last verified: 2025-09