Reducing Risk of Stroke and DementIa In patientS With COVert cERebrovascular Disease

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorUniversity of Edinburgh

About this trial

The purpose of the DISCOVER study is to pilot acceptable approaches to people with covert cerebrovascular disease (CCD) and their follow-up. This is the first step in designing efficient randomised trials of treatments to reduce the risk of stroke or dementia in people with CCD.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

People who, at the time the letter is prepared or are identified by a clinician

Age ≥ 65 years

Stroke or TIA

Dementia

Disqualifiers

Text of brain scan report unreadable

Do not consent to take part in study procedures

Unable to consent

Unable to communicate by email, letter or telephone through language, speech disability or lack of address

Trial population

People aged 65 years or older living in Scotland, UK

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Functional and Cognitive scores

    Other intervention

    We will collect information about prior neurological symptoms, including prior symptoms suggestive of TIA or stroke, cognitive or motor symptoms, blood pressure and other known vascular risk factors, medicines, frailty, functional status, education, and employment status We will collect a baseline validated function and cognitive score, and take a sample of speech. Speech will be measured at assessment, in collaboration with the NeuroCARE Clinical and Digital Measures Module (22/SS/0010 IRAS No. 310885).

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Functional scores

The investigators will measure day-to-day function with the Bristol Activities of Daily Living Scale, which is a 20-item assessment of daily living abilities for dementia. Each activity has 5 statement options (a - e) which refer to a different level of ability.

Time frame
At 3, 6 and 12 months following enrolment
2

Cognitive scores

The investigators will measure concerns or anxiety about covert cerebrovascular disease using the Montreal Cognitive Assessment. It is a 10-minute test that assesses seven areas of cognition for a total possible score of 30 points. A score of 25 or less is indicative of cognitive impairment.

Time frame
At 3, 6 and 12 months following enrolment
3

Speech samples

Speech will be measured at assessment, in collaboration with the NeuroCARE Clinical and Digital Measures Module (22/SS/0010 IRAS No. 310885).

Time frame
At 3, 6 and 12 months following enrolment
4

Vascular events

At each assessment the investigators will ask about dementia, mild cognitive impairment and stroke symptoms.

Time frame
At 3, 6 and 12 months following enrolment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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