CHAMP App Cardiac Study and Repository

Sponsor
Lori Erickson (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT06034392
Collaborator
(none)
1,000
1
25.2
39.6

Study Details

Study Description

Brief Summary

This is a multi-site research study with an optional research repository that will consist of clinically derived data and photographic or video images of patients in the home setting with complex health conditions to evaluate the safety and efficacy of the CHAMPĀ® software platform, with data and photographic or video images input and/or uploaded by the parent or other legally authorized representative (LAR) of patients with complex congenital heart disease as a target population.

Condition or Disease Intervention/Treatment Phase
  • Device: CHAMP App

Detailed Description

Study objectives

  1. To evaluate whether data collection and transmission through the CHAMP software platform improves communication between health care providers and parents/LAR that positively affects the care of children with complex congenital heart disease in which asynchronous monitoring in the home setting is indicated

  2. To determine the accuracy of data obtained regarding observation by parent or caregiver of the condition of children with complex congenital heart disease in which asynchronous monitoring in the home setting is indicated.

  3. To evaluate the use of the CHAMP App for clinical purposes, including user satisfaction with the data entry, parental self-management, and transmission capabilities.

  4. To evaluate the real-world performance analytics (RWPA) of the CHAMP software platform for transfer of parent-entered data for children with complex congenital heart disease in which asynchronous monitoring in the home setting is indicated.

Endpoints

  1. To demonstrate that parents and caregivers for children with complex congenital heart disease in which asynchronous monitoring in the home setting is indicated can accurately identify and transmit to healthcare providers specific health-related data including intake of food, fluids and mediations; output, including urination, defecation, and vomiting; weight; vital signs including oxygen saturation as measured by pulse oximetry; heart rate as measured either by a heart rate monitor or manually by the parent or caregiver; and temperature, measured by a reliable thermometer; and the value and reliability of videos provided by parents and caregivers regarding behavior of pediatric study participants for use in evaluating participant's health status.

  2. To demonstrate that data obtained through the use of devices such as pulse oximeters, as entered into the app by parents and caregivers, provide valuable information regarding the health status of children with Complex Diagnoses in a home setting.

  3. To demonstrate characteristics of CHAMP through real world health analytics (RWHA), user experience analytics (UX), and product performance analytics (PPA).

The study duration is open-ended for safety, effectiveness, and performance of the CHAMP app. Unless consent is withdrawn, data will be kept and used for data analysis and, if consented to the research repository for multi-site research purposes indefinitely. At age 18, previously pediatric patients may be approached for reconsent.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
1000 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
CHAMP App Cardiac Study: Evaluation of Software Functions for Asynchronous Monitoring of Children With Complex Congenital Heart Disease in the Home Setting and Data Repository
Actual Study Start Date :
Aug 25, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Oct 1, 2025

Outcome Measures

Primary Outcome Measures

  1. Human factors/usability engineering: Login failures [Over a 3 month period]

    Rate of attempts of log-in failures

  2. Human factors/usability engineering: Imprecision [Over a 3 month period]

    Rate of data values reported with imprecision

  3. Clinical Safety: Anticipated adverse events [Over a 3 month period]

    Anticipated Adverse event rates

  4. Clinical Safety: Event resolution- anticipated [Time in days, reported over the last 3 months]

    Time to resolve anticipated adverse events

  5. Clinical Safety: Unanticipated Adverse events [Time in days, reported over the last 3 months]

    Unanticipated adverse event rates

  6. Clinical Safety: Event resolution- unanticipated [Time in days, reported over the last 3 months]

    Time to resolve unanticipated adverse events

  7. Health Benefits: Adherence [Measurement of adherence to daily data entry per each patient/parent over 3 month period on non-hospitalized days, during the study period]

    Rate of adherence to daily data entry

  8. User Satisfaction: Complaints [Over a 3 month period]

    Complaint rates via the healthcare team web portal

  9. User Satisfaction CHAMP Video [through study completion, an average of 9 months]

    Feedback from healthcare team will be received via treatment endpoint survey questions. Likert scale questions 1-strongly disagree to 5 strongly agree (Using CHAMP videos for the interstage monitoring of this patient improved clinical decisions for the home monitoring team). Available to put in comments.

  10. User Satisfaction: Communication [through study completion, an average of 9 months]

    Feedback from healthcare team will be received via treatment endpoint survey questions Likert scale questions 1-strongly disagree to 5 strongly agree ( Using CHAMP for the interstage monitoring of this patient improved communication with the parents at home.) Available to put in comments.

  11. User Engagement [Over a 3 month perriod]

    Total number of registered users (Active, treatment endpoint reached) and data totals per parent entered measure. De-identified Demographics and age areas utilization -Utilization across the number of pediatric sites, healthcare teams

  12. CHAMP app performance: Downtime [Over a 3 month period]

    Product Performance Analytics measured through Any system downtime

  13. CHAMP app performance: Cybersecurity [Over a 3 month period]

    Product Performance Analytics measured through Any reported breaches

  14. CHAMP app performance [Quarterly review of CHAMP App Performance will be measure over the preceding 3 months for frequency of changes required]

    Product Performance Analytics measured through --Bug/defect rate or Version failure rates

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 0-17 years with a parent/Legally authorized representative

  • Diagnosed with a complex health condition in which asynchronous monitoring in the home setting is appropriate.

  • Pediatric patient's cardiac care team has decided that the patient's treatment plan may benefit from remote home monitoring.

  • Institution that the subject is followed through clinically has been an approved as site for the CHAMP app study with Children's Mercy Kansas City.

Adult participants

  • Parents/Legally authorized representatives of pediatric subject.

  • Healthcare team users at an institution that is an approved site for the CHAMP app Study with Children's Mercy Kansas City.

Exclusion Criteria:
  • Inability to be discharged to care in the home setting.

  • Those not meeting the above inclusion criteria.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Mercy Hospital Kansas City Missouri United States 64108

Sponsors and Collaborators

  • Lori Erickson

Investigators

  • Principal Investigator: Lori Erickson, PhD, Director, Remote Health Solutions Children's Mercy

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Lori Erickson, Director, Remote Health Solutions, Children's Mercy Hospital Kansas City
ClinicalTrials.gov Identifier:
NCT06034392
Other Study ID Numbers:
  • 15030113CMH
First Posted:
Sep 13, 2023
Last Update Posted:
Sep 18, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Lori Erickson, Director, Remote Health Solutions, Children's Mercy Hospital Kansas City
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 18, 2023