Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 5:38 PM
Ignite Modification Date:
2025-12-24 @ 5:38 PM
NCT ID:
NCT07097168
Brief Summary:
The goal of this observational study is to use the WHOOP device to measure heart rate variability (HRV) in patients with coronary artery disease (CAD) before and after they have CABG (coronary artery bypass graft) surgery. The main questions it aims to answer are:
* Can changes in HRV, measured by the WHOOP device, help predict how well patients with CAD will recover after CABG surgery?
* Can HRV changes during the hospital stay give doctors useful information about the patient's recovery?
Participants will:
* Wear the WHOOP device before and after their CABG surgery to measure HRV.
* Share their health information to help researchers see how changes in HRV are connected to recovery.
This study will help find out if the WHOOP device can be used as a medical tool to track recovery in patients with CAD after CABG surgery.
Study:
NCT07097168
Study Brief:
Protocol Section:
NCT07097168