- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05892952
IONA Longitudinal Cohort Study (IONA LCS)
September 15, 2025 updated by: Brain Health Scotland Life Sciences Ltd
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.
Study Overview
Status
Recruiting
Conditions
Detailed Description
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.
Study Type
Observational
Enrollment (Estimated)
10000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Sarah Gregory, PhD
- Phone Number: 0131 353 0233
- Email: s.gregory@brainsciences.scot
Study Contact Backup
- Name: Joseph Milne
- Email: j.milne@brainsciences.scot
Study Locations
-
-
Lothian
-
Edinburgh, Lothian, United Kingdom, EH12 9DQ
- Recruiting
- Scottish Brain Sciences Arran Facility
-
Contact:
- Craig Ritchie, Prof
- Phone Number: 0131 353 0233
- Email: c.ritchie@brainsciences.scot
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
The IONA LCS is designed to be inclusive and from within this diverse population smaller sub-populations will be derived.
Given the main objective of the programme, the study is open to people over the age of 50 who range from having no symptoms of neurodegenerative disease to those living with a dementia syndrome at the mild stage of illness.
All participants will have the capacity to consent to the study at the baseline.
Participants who develop moderate-to-severe dementia, and those who lose capacity to provide informed consent during the study, will remain in the study to ensure disease models can capture the full trajectories of these diseases.
Recruitment strategies will be designed using the above five sources to ensure all people representative of the Scottish population (ensuring there is representation from different ages, sex, ethnicity, education, socioeconomic status) who are suitable for the IONA LCS are invited to participate.
Description
- 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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change over time on the IONACog (a composite neuropsychological battery)
Time Frame: 10 years
|
10 years
|
|
(Enhanced Phenotype only) Change over time in cerebrospinal fluid amyloid beta-42
Time Frame: 10 years
|
10 years
|
|
(Enhanced Phenotype only) Change over time in cerebrospinal fluid phosphorylated tau 181
Time Frame: 10 years
|
10 years
|
|
(Enhanced Phenotype only) Change over time in cerebrospinal fluid total tau
Time Frame: 10 years
|
10 years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change over time in dependency (as measured by the Stern Dependency Scale)
Time Frame: 10 years
|
10 years
|
|
Change over time in caregiver burden (as measured by the Zarit Burden Index)
Time Frame: 10 years
|
10 years
|
|
Change over time in quality of life (as measured by the QoL-AD)
Time Frame: 10 years
|
10 years
|
|
(Enhanced Phenotype only) impact of disclosure of Alzheimer's disease biomarkers as measured by the Impact of Events scale-6.
Time Frame: 10 years
|
10 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 21, 2023
Primary Completion (Estimated)
December 21, 2033
Study Completion (Estimated)
December 21, 2033
Study Registration Dates
First Submitted
May 29, 2023
First Submitted That Met QC Criteria
May 29, 2023
First Posted (Actual)
June 7, 2023
Study Record Updates
Last Update Posted (Estimated)
September 19, 2025
Last Update Submitted That Met QC Criteria
September 15, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BrainHealthScotland
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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