Utilizing Technology for Optimization of Pain Management and Mobilization in High Risk Cardiac Surgical ICU Patients
Status unconfirmed
Conditions studied: Transplant; Failure, Heart, Heart Failure, Congestive, Lung Transplant Failure
In brief
The purpose of this project is to improve mobility in the perioperative period using activity trackers to augment current practice. Delirium and poor functional status following ICU stays are intractable problems for which clear solutions do not exist. Digital health approaches have not been applied to these problems in the ICU setting and may represent a viable and unexplored intervention. The program will involve the utilization of an activity tracker in ambulating patients. There will be two arms to the program. The first will involve the longitudinal study of ambulating lung transplant patients. Patients will be given an activity tracker at time of transplant which will continue throughout their care into their first month at home. The data will be collected to identify correlation between activity and clinical outcomes.
Key facts
- Study ID
- NCT04146727
- Run by
- Cedars-Sinai Medical Center
- People needed
- 168
- Starts
- 2020-01-01
- Expected to finish
- 2021-06-01
- Last updated by the study team
- 2019-10-31
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients that are at high-risk patients for one of the following interventions, will be considered for this study:
- Axillary impella patients awaiting transplant, advanced MCS therapy or weaning
- MCS patients post procedure including TAH, LVADs
- Lung Transplant patients
- Subjects > 18 years of age.
- Ability to provide informed consent and follow-up with protocol procedures
You may not qualify if…
- Non-ambulatory patients
- Participation in an on-going protocol studying an experimental drug or device
- Use of a walker, cane or wheelchair at baseline
- Inability to wear the biosensor on the wrist
- Any condition or other reason that, in the opinion of the Investigator or Medical Monitor, would render the subject unsuitable for the study
Where it is running
- Cedars-Sinai Medical Center — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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