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NCT00645008 · ClinicalTrials.gov registry record
Identification of Dominate Stressors in the Intensive Care Unit (ICU)
A clinical trial, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- 160
- Enrollment target
NCT00645008 is a clinical trial that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 160 participants.
The verdict
NCT00645008 has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- 160 participants
- Enrollment target
Study Summary
Undergoing cardiopulmonary bypass surgery and the subsequent admission to the intensive care unit (ICU) is known to be a stressful event to the patient. As patients prepare for open-heart surgery it is natural for them to feel anxious and concerned about all the various procedures involved in the process. Members of both the surgical and anesthesia team explain the purpose of each procedure and all issues associated with the procedures in great detail in order to better prepare the patient, ease their anxiety and aid their recovery. The underlying assumption for past investigations into overall patient satisfaction has been that the stressors inherent in the experience of illness and hospitalization have an adverse effect on patient recovery and can possibly prolong the recuperative process. Previous studies have shown that the specific performance of a team in regard to the effects of the stressors on the patient's status is key to providing optimal patient care in the ICU environment. Since the ICU stay is a difficult experience in the life of a patient, stressor predictability might allow for better physical and psychological conditions for the patient's recovery. Although there is a myriad of published research available on the potential stressors related to an ICU stay, there is a dearth of investigation into the inherently more intense circumstances surrounding a stay in the Cardiothoracic Intensive Care Unit (CT-ICU). By examining the stressors in the CT-ICU changes can be made by the medical care team and/or hospital that can ultimately enhance the patient experience in the CT-ICU. The purpose of this study is to reduce or completely eliminate stressors present in the CT-ICU as identified by the cardiac bypass patient. Identification of events and conditions considered stressful in the ICU will allow the professional team to determine which stressors are amendable to intervention and tailor patient care accordingly.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2008-04 |
| Est. Completion | 2013-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00645008
The ClinicalTrials.gov registry entry for NCT00645008 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT00645008 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00645008 about?
NCT00645008 is a clinical study titled "Identification of Dominate Stressors in the Intensive Care Unit (ICU)". Undergoing cardiopulmonary bypass surgery and the subsequent admission to the intensive care unit (ICU) is known to be a stressful event to the patient. As patients prepare for open-heart surgery it is natural for them to feel anxious and concerned about all the various procedures involved in the pr...
What is the current status of trial NCT00645008?
This trial is currently completed. The enrollment target is 160 participants. The study started on 2008-04. Estimated completion is 2013-06.
Who is sponsoring clinical trial NCT00645008?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
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