Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to determine whether a prototype toilet device that we have developed can accurately and automatically track human fluid output from renal and gastrointestinal systems in the hospital. The device includes components that can be outfitted onto existing toilets.
In this study, participants hospital room will be outfitted with the prototype toilet device. Participants will use the toilet as usual throughout the duration of their inpatient stay. Sometimes output will be measured by the device, and other times output will be measured manually by nurses.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Device | Experimental | Patients use toilet device to measure fluid output and self-report event types |
|
| Control | No Intervention | Collection in standard hats + nurses visually assessing fluid volumes |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Electronic Device for Toilet | Device | Device will be installed on toilet of patients will in hospital to measure all waste output. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Mean absolute error of urine volume (in mL) as measured by device compared to standard of care nurse assessment | Up to 14 days |
| Measure | Description | Time Frame |
|---|---|---|
| Correlation between daily patient fluid balance (difference between fluid input and output in mL) as measured by device measurements or standard of care nurse assessment and the change in daily weight | Up to 14 days | |
| Mean absolute error of urine volume (in mL) as measured by device |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Lauren Hill | Contact | 919-668-2369 | lauren.hill@duke.edu | |
| Amy Bush | Contact | +1 919 668 1085 | amy.bush@duke.edu |
| Name | Affiliation | Role |
|---|---|---|
| Chenyu Lin, MD | Duke University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Duke University | Recruiting | Durham | North Carolina | 27705 | United States |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D000072296 | Bathroom Equipment |
| ID | Term |
|---|---|
| D004864 | Equipment and Supplies |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Up to 14 days |
| Time (in mins) spent handling/recording patient waste | First 3 days of patient's HCT conditioning |
| Levels of chemotherapy drugs detectable on room surfaces as measured by surface testing | First 3 days of patient's HCT conditioning |
| Time (in mins) between nurse logging of patient urination in electronic medical records and device-based logging of patient urination | Up to 14 days |
| Percent device can correctly identify diarrhea events | Up to 14 days |
| Percent of patients who indicated device satisfaction as measured by patient survey | Day 3 of HCT conditioning |
| Percent of nurses who perceived lower chemotherapy exposure as measured by survey | After transition to Stage 2 - about 3 days after patient begins HCT conditioning |
| Percent of nurses who indicated device satisfaction as measured by nurse survey | After transition to Stage 2 - about 3 days after patient begins HCT conditioning |
| Number of patient falls as measured by patient report | Up to 17 days |