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Recruiting NCT07058064

NCT07058064 WATCH (Wearable Artificial inTelligence for Cardiac Function and Health Monitoring)

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Clinical Trial Summary
NCT ID NCT07058064
Status Recruiting
Phase
Sponsor Mayo Clinic
Condition Lymphoma
Study Type INTERVENTIONAL
Enrollment 250 participants
Start Date 2025-07-18
Primary Completion 2029-06-29

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
All Conditions
Interventions
ElectrocardiogramEchocardiogramLVEF echocardiogram

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 250 participants in total. It began in 2025-07-18 with a primary completion date of 2029-06-29.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to find a cost effective cardiovascular (CV) surveillance of cancer survivors over long periods of time to prevent the risk of progression of heart failure (HF) and related morbidity and mortality. Mobile device-based artificial intelligence (AI)-electrocardiogram (ECG) can reliably detect cardiac dysfunction in lymphoma and sarcoma survivors and smart watch based surveillance for cardiotoxicity is feasible and reliable.

Eligibility Criteria

Inclusion Criteria: * ability to understand study procedures and being willing to comply with them for the entire study length * diagnosis of lymphoma or sarcoma with new start or 1 year after completion of anthracycline therapy Exclusion Criteria: * LVEF \<50% at baseline, or prior confirmed history of heart failure, persistent atrial fibrillation, left bundle branch block, or paced rhythm * Unwilling or unable to give written informed consent * Participants who have opted out of the Minnesota Research Authorization

Contact & Investigator

Central Contact

Tera Peck

✉ Peck.Tera@mayo.edu

📞 507-266-2123

Principal Investigator

Joerg Herrmann, MD

PRINCIPAL INVESTIGATOR

Mayo Clinic

Frequently Asked Questions

Who can join the NCT07058064 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Lymphoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07058064 currently recruiting?

Yes, NCT07058064 is actively recruiting participants. Contact the research team at Peck.Tera@mayo.edu for enrollment information.

Where is the NCT07058064 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT07058064 clinical trial?

NCT07058064 is sponsored by Mayo Clinic. The principal investigator is Joerg Herrmann, MD at Mayo Clinic. The trial plans to enroll 250 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology