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MyHeartBaby: An Initial Evaluation of the MyHeartBaby Psychosocial Telemedicine Program

Primary Purpose

Congenital Heart Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MyHeartBaby Program
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Congenital Heart Disease focused on measuring CHD, Congenital Heart Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Caregiver's infant is less than 45 days of age at time of study enrollment.
  • Caregiver of infant with high-risk, shunt dependent physiology (one or two-ventricle circulation) having just received neonatal surgery for CHD.
  • English is a primary language for caregiver of infant.

Exclusion Criteria:

  • Caregiver's infant is greater than 45 days of age at time of study enrollment.
  • Not a caregiver of infant with high-risk, shunt dependent physiology having just received neonatal surgery for CHD.
  • English is not a primary language for caregiver of infant.

Sites / Locations

  • Children's Healthcare of Atlanta

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

MyHeartBaby

Standard of Care

Arm Description

Caregivers will complete Telehealth Psychosocial Sessions and 4 follow up assessments.

Caregivers will complete 4 follow up assessments.

Outcomes

Primary Outcome Measures

Change in Levels Stress for Caregivers of 1-Ventricle Cardiac Defect Infants
Stress levels will be measured by the Pediatric Inventory for Parents (PIP) which is a 42-item measure that assesses disease-related parenting stress and asks caregivers to indicate the frequency at which disease-related parenting stressor occurs, and the difficulty-level of each stressor.
Change in Levels Stress for Caregivers of 2-Ventricle Cardiac Defect Infants
Stress levels will be measured by the Pediatric Inventory for Parents (PIP) which is a 42-item measure that assesses disease-related parenting stress and asks caregivers to indicate the frequency at which disease-related parenting stressor occurs, and the difficulty-level of each stressor.

Secondary Outcome Measures

Change in Levels of Caregiver Confidence in Feeding Management for 1-Ventricle Cardiac Defect Infants
The confidences in feeding questionnaire has been developed for purposes of this study and has a list of 20 questions that ask caregivers about daily feeding practices, stress associated with feeding, and ability to soothe infant.
Change in Levels of Caregiver Confidence in Feeding Management for 2-Ventricle Cardiac Defect Infants
The confidences in feeding questionnaire has been developed for purposes of this study and has a list of 20 questions that ask caregivers about daily feeding practices, stress associated with feeding, and ability to soothe infant.
Change in Infant Weight for 1-Ventricle Cardiac Defect Infants
Clinical assessments of weight-for-age percentiles for purposes of study outcomes will be obtained during regularly scheduled clinic visits.
Change in Infant Weight for 2-Ventricle Cardiac Defect Infants
Clinical assessments of weight-for-age percentiles for purposes of study outcomes will be obtained during regularly scheduled clinic visits.
Number of Unplanned Hospital Admissions
Caregivers will report infant hospital admissions during the study duration.

Full Information

First Posted
September 6, 2016
Last Updated
July 10, 2017
Sponsor
Emory University
Collaborators
Pediatric Heart Network, National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT02895334
Brief Title
MyHeartBaby: An Initial Evaluation of the MyHeartBaby Psychosocial Telemedicine Program
Official Title
An Initial Evaluation of the MyHeartBaby Psychosocial Telemedicine Program
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
July 2015 (Actual)
Primary Completion Date
April 7, 2017 (Actual)
Study Completion Date
April 7, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Pediatric Heart Network, National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will conduct an initial clinical evaluation of this support program to examine its impact on reducing caregiver stress, increasing confidence in daily feeding, and improving weight-for-age growth percentiles in infants with Congenital Heart Disease (CHD).
Detailed Description
Caregivers of infants with CHD are at high-risk of anxiety and distress due to the complex daily caregiving demands. Previous research has demonstrated decreased parental stress and more optimal infant developmental outcomes with a psychosocial intervention delivered to caregivers of infants with CHD prior to hospital discharge as well as reduced healthcare use in caregivers who received medical video-consultations during the interstage surgical palliation period. This study will implement a telemedicine intervention program (MyHeartBaby) to support caregivers remotely in the daily care and adjustment to having an infant with chronic medical needs. The program is delivered via video chat over the Internet and caregivers will complete questionnaires about general family information, stress, and feeding their infant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease
Keywords
CHD, Congenital Heart Disease

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
MyHeartBaby
Arm Type
Experimental
Arm Description
Caregivers will complete Telehealth Psychosocial Sessions and 4 follow up assessments.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Caregivers will complete 4 follow up assessments.
Intervention Type
Behavioral
Intervention Name(s)
MyHeartBaby Program
Intervention Description
Participating Caregivers will receive an electronic tablet loaded with a telemedicine intervention program (MyHeartBaby) to support caregivers remotely in the daily care and adjustment to having an infant with chronic medical needs with video-based telemedicine support services. There are a total of six sessions occurring at weeks 3, 6, 9, 12, and 15 of the study.
Primary Outcome Measure Information:
Title
Change in Levels Stress for Caregivers of 1-Ventricle Cardiac Defect Infants
Description
Stress levels will be measured by the Pediatric Inventory for Parents (PIP) which is a 42-item measure that assesses disease-related parenting stress and asks caregivers to indicate the frequency at which disease-related parenting stressor occurs, and the difficulty-level of each stressor.
Time Frame
Baseline, Week 18
Title
Change in Levels Stress for Caregivers of 2-Ventricle Cardiac Defect Infants
Description
Stress levels will be measured by the Pediatric Inventory for Parents (PIP) which is a 42-item measure that assesses disease-related parenting stress and asks caregivers to indicate the frequency at which disease-related parenting stressor occurs, and the difficulty-level of each stressor.
Time Frame
Baseline, Week 18
Secondary Outcome Measure Information:
Title
Change in Levels of Caregiver Confidence in Feeding Management for 1-Ventricle Cardiac Defect Infants
Description
The confidences in feeding questionnaire has been developed for purposes of this study and has a list of 20 questions that ask caregivers about daily feeding practices, stress associated with feeding, and ability to soothe infant.
Time Frame
Baseline, Week 18
Title
Change in Levels of Caregiver Confidence in Feeding Management for 2-Ventricle Cardiac Defect Infants
Description
The confidences in feeding questionnaire has been developed for purposes of this study and has a list of 20 questions that ask caregivers about daily feeding practices, stress associated with feeding, and ability to soothe infant.
Time Frame
Baseline, Week 18
Title
Change in Infant Weight for 1-Ventricle Cardiac Defect Infants
Description
Clinical assessments of weight-for-age percentiles for purposes of study outcomes will be obtained during regularly scheduled clinic visits.
Time Frame
Baseline, Week 18
Title
Change in Infant Weight for 2-Ventricle Cardiac Defect Infants
Description
Clinical assessments of weight-for-age percentiles for purposes of study outcomes will be obtained during regularly scheduled clinic visits.
Time Frame
Baseline, Week 18
Title
Number of Unplanned Hospital Admissions
Description
Caregivers will report infant hospital admissions during the study duration.
Time Frame
Week 18

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Caregiver's infant is less than 45 days of age at time of study enrollment. Caregiver of infant with high-risk, shunt dependent physiology (one or two-ventricle circulation) having just received neonatal surgery for CHD. English is a primary language for caregiver of infant. Exclusion Criteria: Caregiver's infant is greater than 45 days of age at time of study enrollment. Not a caregiver of infant with high-risk, shunt dependent physiology having just received neonatal surgery for CHD. English is not a primary language for caregiver of infant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brandon Aylward
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Healthcare of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

MyHeartBaby: An Initial Evaluation of the MyHeartBaby Psychosocial Telemedicine Program

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