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Evaluating the Value of Telehealth for Care of Children With Medical Complexity

Primary Purpose

Cerebral Palsy

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
TytoCare Device
Sponsored by
Advocate Health Care
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Cerebral Palsy focused on measuring children with medical complexity, Telemedicine, Tracheostomy

Eligibility Criteria

1 Month - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient aged 1 month to 18 years
  • Patient currently enrolled in CCCMC program at ACH-OL
  • Parental permission/consent
  • English-speaking (at least one parent)
  • Internet connected home wi-fi

Exclusion Criteria

  • Unable to comply with study requirements

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    No Intervention

    Experimental

    Arm Label

    Control Group

    Telemedicine Group

    Arm Description

    Usual care

    TytoCare Device

    Outcomes

    Primary Outcome Measures

    Frequency of In-person Health Care Encounters
    Hospital day length of stay reported as the total number of hospital days in the group.

    Secondary Outcome Measures

    Provider Survey
    Success of connection for telemedicine visits.
    Parent Survey
    Overall satisfaction with device, comfort with Device, satisfaction with clinician interactions and development of plans of care; Questions asked using 4 point Likert scale (4 = Very Satisfied , 1=Very Dissatisfied). Higher score more satisfaction

    Full Information

    First Posted
    July 27, 2016
    Last Updated
    January 16, 2019
    Sponsor
    Advocate Health Care
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02849938
    Brief Title
    Evaluating the Value of Telehealth for Care of Children With Medical Complexity
    Official Title
    Evaluating the Value of Telehealth for Care of Children With Medical Complexity
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2016 (undefined)
    Primary Completion Date
    January 31, 2017 (Actual)
    Study Completion Date
    March 20, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Advocate Health Care

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The specific aims of the study are to: Assess the feasibility of a TytoCare telehealth device with remote audio/video connection for evaluation of children with medical complexity in the home environment. Evaluate the usability of a TytoCare telehealth device in transmitting real time images (otoscope, oropharyngeal exam, camera), temperature, and sound (stethoscope for heart and breath sounds) Compare the impact of the TytoCare telehealth device versus traditional telephone assessment on patient management and user satisfaction
    Detailed Description
    Eligible children of interested parent(s) will be randomly assigned to either the control group (standard care) or the intervention group (Tyto device). Randomization will be performed using an online randomization program to generate group assignments for the 25 subjects. Subjects will be stratified by whether they have a tracheostomy or not and be assigned 1.5:1 to achieve 15 children in the device group and 10 children in the control group. Informed consent will be obtained for children in each group. Children/families in the control group will continue to get usual care through the CCCMC program, and will be able to access their providers via telephone for urgent care needs and scheduled follow up. For evaluation purposes, data collection will include the monthly encounter tracking that is done routinely as part of the CCCMC program, and research surveys completed by both parents and HCPs. Parents will complete a Parent Survey by phone once each month for the 3-month study period. The CCCMC HCPs will complete the Provider Survey electronic survey with each telephone encounter where the HCP would have liked to use the device. For those assigned to the device group, parents will be instructed to contact their CCCMC HCP as usual, see bullet points above, when health concerns arise and their HCP will decide if she would like a telehealth visit. Telehealth/video visits may also be scheduled in advance as a matter of routine follow-up care. In the event that an exam is deemed necessary by the HCP, the parent or caregiver will be directed to connect via the remote exam device. The provider will conduct a 2-way live interactive audio/video visit with the patient. The parent or caregiver will use the remote exam device to provide temperature, lung sounds, heart sounds, oropharyngeal exam, skin exam and/or ear exam as clinically indicated. Direction for necessary treatment, referral to an ED, clinic or inpatient care will be at the discretion of the CCCMC provider. For evaluation purposes, in addition to the monthly encounter tracking that is done as part of the CCCMC program, both parents and HCPs will complete surveys. Parents will complete a Parent Survey by phone once each month for the 3-month study period. The CCCMC HCPs will complete the Provider Survey via a Qualtrics link with each telehealth encounter. Additional data collected will include subject demographics, and encounter data that is routinely collected as a part of the CCCMC program. Images of patient encounters will be transmitted in real time via the telemedicine device encrypted software. Provider Survey data will be gathered via Qualtrics. Tyto will retain / store data obtained from device group encounters in a de-identified way for development purposes only.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cerebral Palsy
    Keywords
    children with medical complexity, Telemedicine, Tracheostomy

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    24 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Control Group
    Arm Type
    No Intervention
    Arm Description
    Usual care
    Arm Title
    Telemedicine Group
    Arm Type
    Experimental
    Arm Description
    TytoCare Device
    Intervention Type
    Device
    Intervention Name(s)
    TytoCare Device
    Intervention Description
    Tyto is a handheld, mobile device designed for capture and transmission of ear/throat/skin images and lung/heart auscultations. It may be used to perform non-invasive, medical examinations, either on a patient (by another person, most commonly a family member, or by a medical professional) or self-performed by the patient, for remote review by a medical practitioner. It is suitable for use on patients in both clinical and home environment.
    Primary Outcome Measure Information:
    Title
    Frequency of In-person Health Care Encounters
    Description
    Hospital day length of stay reported as the total number of hospital days in the group.
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Provider Survey
    Description
    Success of connection for telemedicine visits.
    Time Frame
    3 months
    Title
    Parent Survey
    Description
    Overall satisfaction with device, comfort with Device, satisfaction with clinician interactions and development of plans of care; Questions asked using 4 point Likert scale (4 = Very Satisfied , 1=Very Dissatisfied). Higher score more satisfaction
    Time Frame
    3 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Month
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patient aged 1 month to 18 years Patient currently enrolled in CCCMC program at ACH-OL Parental permission/consent English-speaking (at least one parent) Internet connected home wi-fi Exclusion Criteria Unable to comply with study requirements
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Patricia M Notario, MD
    Organizational Affiliation
    Advocate Children's Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Will share only aggregate and overall project results through poster and/or oral presentations at local, regional and national meetings.
    Citations:
    PubMed Identifier
    30628860
    Citation
    Notario PM, Gentile E, Amidon M, Angst D, Lefaiver C, Webster K. Home-Based Telemedicine for Children with Medical Complexity. Telemed J E Health. 2019 Nov;25(11):1123-1132. doi: 10.1089/tmj.2018.0186. Epub 2019 Jan 30.
    Results Reference
    derived

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    Evaluating the Value of Telehealth for Care of Children With Medical Complexity

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