i-Dashboard for Multi-disciplinary Rounds in SICU
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04845698 |
|
Recruitment Status :
Completed
First Posted : April 15, 2021
Last Update Posted : September 1, 2021
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Background: Information overload is a common problem in intensive care units. A display tool that facilitates retrieval of crucial clinical information from electronic medical records has excellent potential to attenuate information overload and benefit workflow.
Study hypothesis: In this project, we aimed to evaluate the efficacy and clinical satisfaction of a team-designed, patient-centered electronic medical record viewer, i-Dashboard, to facilitate multi-disciplinary rounds in our surgical intensive care units.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Workflow Communication Quality of Health Care | Device: i-Dashboard | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 144 participants |
| Allocation: | Randomized |
| Intervention Model: | Crossover Assignment |
| Intervention Model Description: | A cluster randomized trial was conducted in two surgical intensive care units (ICUs) of the hospital. For each two-week period of the trial, participating ICUs (cluster) were assigned to multi-disciplinary rounds with i-Dashboard (intervention) or without i-Dashboard (control). In other words, the two ICUs were randomly assigned to multi-disciplinary rounds with i-Dashboard during the first two weeks, without i-Dashboard during the second two weeks, and with i-Dashboard during the third two weeks or vice versa. |
| Masking: | None (Open Label) |
| Primary Purpose: | Health Services Research |
| Official Title: | Application of i-Dashboard for Multi-disciplinary Rounds in Surgical Intensive Care Units |
| Actual Study Start Date : | April 26, 2021 |
| Actual Primary Completion Date : | July 18, 2021 |
| Actual Study Completion Date : | July 18, 2021 |
| Arm | Intervention/treatment |
|---|---|
|
Experimental: With i-Dashboard
Multi-disciplinary rounds are conducted with the assistance of i-Dashboard.
|
Device: i-Dashboard
i-Dashboard is a team-designed, patient-centered electronic medical record viewer, which retrieves data from multiple databases and provides a quick representation of essential metrics for each patient. |
|
No Intervention: Without i-Dashboard
Multi-disciplinary rounds are conducted without the assistance of i-Dashboard. The team members collect data using standard electronic medical records.
|
- Time spent on pre-round data gathering (minutes) [ Time Frame: 3 hours ]Pre-round data gathering for multi-disciplinary rounds in ICUs is usually time-consuming. i-Dashboard, the team-designed display tool that facilitates retrieval of crucial clinical information from electronic medical records, is available on every computer screen in the ICU. We aim to evaluate whether i-Dashboard might help reduce time spent on pre-round data gathering for each patient evaluated during multi-disciplinary ICU rounds.
- Communication accuracy during multi-disciplinary ICU rounds (number of data misrepresentation) [ Time Frame: 3 hours ]Communication during multi-disciplinary ICU rounds relies primarily on handwritten notes. Based on the literature review, data misrepresentation commonly occurs during ICU rounds, and thus communication accuracy is highly questionable. i-Dashboard, the team-designed display tool, is designed to post the information on a 55-inch screen. We aim to evaluate whether i-Dashboard might help improve communication accuracy during multi-disciplinary ICU rounds.
- Enhancement of care quality and patient safety during multi-disciplinary ICU rounds (number of recommendations from multi-disciplinary team members) [ Time Frame: 3 hours ]Multi-disciplinary team members in ICU (i.e., respiratory therapists, pharmacists and dietitians) provide their recommendations based on patients' condition and their own knowledge and expertise. These recommendations might be adopted by other team members. i-Dashboard, the display tool reporting the information on a large screen, might keep the multi-disciplinary team on the same page and help the members perceive patients' condition and other members' considerations. Thus, persuasive recommendations that enhance care quality and patient safety might be increased during multi-disciplinary rounds.
- Healthcare provider satisfaction (questionnaire) [ Time Frame: 3 months ]i-Dashboard might facilitate the multi-disciplinary ICU rounds and thus enhance healthcare provider satisfaction. The healthcare provider satisfaction will be evaluated by questionnaires modified from previous studies.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients admitted into the two surgical intensive care units for more than 7 days
Exclusion Criteria:
- None
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04845698
| Taiwan | |
| National Cheng Kung University Hospital | |
| Tainan City, Taiwan, R.o.c, Taiwan, 704 | |
| Principal Investigator: | Chao-Han Lai, MD, PhD | National Cheng-Kung University Hospital | |
| Principal Investigator: | Meng-Ru Shen, MD, PhD | National Cheng-Kung University Hospital |
| Responsible Party: | Chao-Han Lai, MD, PhD, National Cheng-Kung University Hospital |
| ClinicalTrials.gov Identifier: | NCT04845698 |
| Other Study ID Numbers: |
B-ER-110-040 |
| First Posted: | April 15, 2021 Key Record Dates |
| Last Update Posted: | September 1, 2021 |
| Last Verified: | August 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Electronic Health Records User-Computer Interface Intensive Care Units Patient Care Team Teaching Rounds |

