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

U

University of Edinburgh

Status

Not yet enrolling

Conditions

Covert Cerebrovascular Disease

Treatments

Other: Functional and Cognitive scores

Study type

Observational

Funder types

Other

Identifiers

NCT06878430
HIPS/23/02 (Other Grant/Funding Number)
AC25041

Details and patient eligibility

About

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.

Full description

DISCOVER is a prospective cohort involving individuals with covert cerebrovascular disease (CCD) in NHS Lothian. Participants will be recruited through electronic health records and clinician collaborators. Participants will be monitored at 3 and 6 months and where possible 12 months to assess cognitive, functional, and vascular event outcomes.

Enrollment

100 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

    • Age ≥ 65 years

    • Have no known history of:

      • Stroke or TIA
      • Dementia
      • Parkinson's disease
      • Multiple sclerosis
      • Metastatic cancer (or non-meningioma brain tumour).
    • A CT or MRI scan report ≤5 years before study start date with of one or more of:

      • Cerebral small vessel disease
      • Deep old ischaemic stroke
      • Cortical old ischaemic stroke

Exclusion criteria

  • 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
  • Unlikely to survive one year past enrolment in judgement of the study investigator

Trial contacts and locations

0

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Central trial contact

William Whiteley

Data sourced from clinicaltrials.gov

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