Your smartwatch may predict a heart attack days before it happens
NCT ID NCT07735338
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This trial tests whether a smartphone app called Antshrike, paired with a smartwatch, can predict heart attacks or strokes within 3-4 days in people at high risk. Participants aged 40 to 79 with existing heart disease or elevated risk will wear the smartwatch for 18 months while the app collects health and lifestyle data. The goal is to see if the app can accurately forecast cardiovascular events like heart attack or stroke in real time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a smartphone application called Antshrike that collects health data via a smartwatch
- What this could lead to
- If accurate, this app could give early warnings of heart attack or stroke, potentially saving lives through faster medical response.
- What could go wrong
- This is an early-stage diagnostic trial with 300 participants. The app may not be accurate enough for real-world use, and false alarms could cause unnecessary stress or medical visits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 to 79 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Be able to provide electronic or written informed consent and be able to effectively communicate and understand the study procedures, risks, and required activities. 2. Age 40 to 79 years. 3. Be willing to wear a smartwatch continuously for 18 months and comfortable with using wearable devices or other technologies that monitor their data over time. 4. Established ASCVD or at an increased risk for a first MACE (i.e., no prior major ASCVD event), defined as anyone of the following: i) Evidence of atherosclerotic CAD on CT or invasive coronary angiogram defined as a coronary artery stenosis ≥ 20% but \<50% in the left main coronary artery or a stenosis ≥ 20% but \<70% in any other major coronary artery. ii) Coronary artery calcium score ≥ 100 Agatston units. iii) High estimated10-year ASCVD risk ≥ 20% by pooled cohort equation. iv) Intermediate estimated 10-year ASCVD risk 7.5% to \<20% by pooled cohort equation with at least 2 of the following risk-enhancing factors: 1. A first degree relative with history of premature ASCVD (males, age \<55 years; females, age \<65 years). 2. History of premature menopause before age 40. 3. History of maternal pregnancy complications (defined as a history of either preeclampsia, gestational hypertension, or gestational diabetes). 4. South Asian ancestry. 5. Chronic inflammatory disorders (defined as either rheumatoid arthritis, systemic lupus erythematosus, psoriasis covering ≥10% of body surface area, Crohn's disease, ulcerative colitis, or HIV/AIDS). 6. High-sensitivity C-reactive protein (hsCRP) ≥2 mg/L documented in the 12 months preceding the screening visit, and, in absence of any underlying acute or inflammatory conditions. 7. Lipoprotein (a) ≥50 mg/dL or ≥125 nmol/L at any time before the screening visit. 8. Estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73 m2. 9. Ankle branchial index (ABI) \<0.9 with no symptoms of intermittent claudication. 10. Metabolic syndrome: increased waist circumference, elevated triglycerides, elevated blood pressure, elevated glucose, and low HDL-C are factors i. Diabetes Exclusion Criteria: 1. The 10-year ASCVD risk \<7.5%. 2. Elevated troponin at baseline. 3. Cognitive impairment. 4. Neurological disorders that would impair their ability to provide informed consent or adhere to study protocols. 5. Metastatic cancer or active cancer undergoing chemotherapy. 6. Terminal illness. 7. Pregnant women or women of childbearing potential not using contraception. 8. Current or past major psychiatric disorders (e.g., schizophrenia, bipolar disorder, severe depression) that could affect physiological or biometric data. 9. Surgical or medical condition, which in the opinion of the Investigator, may place the participant at higher risk from his/her participation in the study, or is likely to prevent the participant from complying with the requirements of the study or completing the study. 10. Unwillingness or inability to comply with study procedures, including adherence to study visits, fasting blood draws and compliance with study protocol. 11. Residing in an inpatient facility or bedbound
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Stanford University
Stanford, California, 94305, United States
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