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Cardiac Monitoring of Post-Operative Cancer Patients Experiencing Atrial Fibrillation

Feasibility of Remote Cardiac Monitoring of Post-Operative Cancer Patients Experiencing Atrial Fibrillation

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01253590
Enrollment
5
Registered
2010-12-03
Start date
2010-12-31
Completion date
2011-11-30
Last updated
2015-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibrillation, Post-Operative Cancer Patients Experiencing Atrial

Keywords

atrial fibrillation, ECG monitor, Blood pressure device, Remote Cardiac Monitoring

Brief summary

The purpose of this study is to assess whether it is possible and acceptable to monitor patients at a distance who experience a condition called atrial fibrillation after their cancer surgery. Some patients have no other clinical reason for staying in the hospital after cancer surgery except in order to control their heart rhythm. Being able to send these patients home earlier and monitor them at a distance from their home can be good for their quick recovery. Studies have shown greater quality of life and patient satisfaction when patients are monitored at a distance for conditions like atrial fibrillation, however cancer patients have not been studied.

Interventions

BEHAVIORALquestionnaire about the use of ECG device

Patients will be fitted with a continuous ECG monitor and blood pressure device. Data on every heart beat, including episodes of atrial fibrillation, for 4-6 weeks of continuous monitoring will be collected and transmitted wirelessly. Based on this information and blood pressure readings performed by patients in their home setting, clinicians can adjust oral coagulant dosage. Participants will attend 2 follow-up outpatient visits at the MSKCC outpatient cardiology practice upon the cardiologist's recommendation. Upon completion of the study, 4-6 weeks, a questionnaire will be sent via mail, including a pre-paid envelope, to participants to assess feasibility, acceptance, and overall experience with remote cardiac monitoring.

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
22 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Post-Operative cancer patients experiencing atrial fibrillation and otherwise clinically ready to be discharged. * Must attend two outpatient visits at MSKCC's cardiology practice during the study period, as specified by the participant's Attending. * Must be older than 21 years of age.

Exclusion criteria

* Non-English speaking patients

Design outcomes

Primary

MeasureTime frameDescription
Assess the feasibility and acceptance of continuous remote cardiac monitoring4 to 6 weeksIn post-operative patients with respect to recurrence of post-operative atrial fibrillation upon discharge.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026