BridgeMD
Prevention study for Stroke
Official title Application of Digital Twins' Technology in Patients Who Had a Stroke, With Moyamoya Disease and With Cerebral Amyloid Angiopathy (CAA) During the Secondary Prevention Phase: A Proof of Concept Using a Randomized Control Trial (Clinical Study 6, STRATIF-AI Project)
ClinicalTrials.gov ID: NCT06714097
What this study is testing
- What it's testing
- The goal of this clinical trial is to obtain initial feedback on the implementation of the STRATIF-AI platform and digital twin in the secondary prevention phase in patients with stroke, Moyamoya disease and Cerebral amyloid angiopathy, including adults of both sexes. The main questions it aims to answer is: how is the patients' experience regarding the use of the STRATIF-AI platform?
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- People aged ≥ 18
- Clinical and neuroradiological diagnosis of stroke (TAC or MR); diagnosis of CAA based on Boston 2.0 criteria; diagnosis of Moyamoya disease based on...
- MOCA total score ≥ 23
- modified Rankin Scale (mRS) ≤ 2
- First-time patients at the Besta Institute
You likely can't join if
- Patients with transient neurological deficits that resolve within an hour and normal brain imaging
- Patient under legal protection or deprived of liberty by judicial or administrative decision
- Patient whose follow-up will be impossible
- Contraindication to magnetic resonance imaging and/or Digital subtraction angiography (DSA)
- Pregnant patients
- Known or suspected drug or alcohol abuse
See the full eligibility criteria
- People aged ≥ 18
- Clinical and neuroradiological diagnosis of stroke (TAC or MR); diagnosis of CAA based on Boston 2.0 criteria; diagnosis of Moyamoya disease based on diagnostic criteria 2021.
- MOCA total score ≥ 23
- modified Rankin Scale (mRS) ≤ 2
- First-time patients at the Besta Institute
- Ability to sign informed consent
- Possibility of performing a brain MRI
- Patients with transient neurological deficits that resolve within an hour and normal brain imaging
- Patient under legal protection or deprived of liberty by judicial or administrative decision
- Patient whose follow-up will be impossible
- Contraindication to magnetic resonance imaging and/or Digital subtraction angiography (DSA)
- Pregnant patients
- Known or suspected drug or alcohol abuse
The study team makes the final eligibility decision.
Where it's taking place
- Milan, Michigan, Italy
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Milan, Michigan, Italy. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.