Testing a Device for Automatically TRacking Urine and STool in an Inpatient HCT Setting (Project TRUST)

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

54 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-13

Study Completion Date

2026-06-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Fluid Output

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Device

Patients use toilet device to measure fluid output and self-report event types

Group Type EXPERIMENTAL

Electronic Device for Toilet

Intervention Type DEVICE

Device will be installed on toilet of patients will in hospital to measure all waste output.

Control

Collection in standard hats + nurses visually assessing fluid volumes

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Electronic Device for Toilet

Device will be installed on toilet of patients will in hospital to measure all waste output.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Scheduled to undergo an allogeneic or autologous hematopoietic stem cell transplant for any cancer or non-cancer illness through the Duke ABMT clinic
* Age 18-80 years
* Karnofsky Performance Scale KPS ≥ 70
* Able to read/write English

Exclusion Criteria

* Inability to use toilet device due to physical constraints, e.g. waste excreted through stoma or catheter
* Physician recommendation that patient does not use standard urine/stool collection hat during days 1-2 of HCT conditioning

Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No