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Behavioural Intervention
Baby2Home Mobile Application for Mental Health Wellness
N/A
Waitlist Available
Research Sponsored by Women and Infants Hospital of Rhode Island
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age 18 years old or greater
Viable term infant (≥ 37 weeks)
Must not have
Infant requires NICU admission
SARS-CoV-2 infection without clinical clearance
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline through 1 year postpartum
Awards & highlights
No Placebo-Only Group
Summary
This trial tests Baby2Home, a digital program to help new parents and their babies. It aims to improve health outcomes and reduce disparities for families affected by COVID-19. The program provides education, wellness tracking, mental health support, and regular check-ins.
Who is the study for?
This trial is for new parents with a healthy, full-term baby (≥37 weeks) born at specific hospitals. Participants must be over 18, speak English, have smartphone access and an email address. It's not for those whose infant passed away or needs NICU care, have severe mental illness, are in certain other studies, experienced IPV with the current partner or lack clinical clearance post-COVID-19 infection.
What is being tested?
The Baby2Home Mobile Application is being tested to see if it can improve healthcare service use and parental outcomes during the first year after birth compared to usual care. The study also looks at whether it reduces health disparities based on race/ethnicity and income.
What are the potential side effects?
Since this trial involves a mobile application rather than medication or medical procedures, traditional side effects are not applicable. However, users may experience issues related to app usability or increased screen time.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
My baby was born at or after 37 weeks of pregnancy.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My infant needs to be admitted to the NICU.
Select...
I currently have a COVID-19 infection without recovery.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline through 1 year postpartum
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline through 1 year postpartum
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Completion of preventive health services utilization for all family members (birthing, non-birthing, and infant)
Secondary study objectives
Anxiety symptoms (for birthing and non-birthing parent)
Breastfeeding self-efficacy (for birthing parent)
COVID-19 related impact (for birthing and non-birthing parent)
+15 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Baby2Home InterventionExperimental Treatment1 Intervention
Families randomized to the intervention arm will receive the B2H services. B2H is a novel digitized CC-based intervention delivered via a smartphone app available on iOS or Android phones, built by combining two successful programs: NICU2Home+ app and CC services. Using the UCD methodologies, AI-based communication within the app will include education for mothers and fathers on the standard of care regarding self-care and newborn care after hospital discharge as well as education, reminders and scheduling for recommended preventative healthcare services for themselves and their new infant.
Group II: Usual CareActive Control1 Intervention
As a pragmatic trial, usual care will be defined by contemporary clinical standards. For maternal care, this includes a comprehensive medical visit between 4-12 weeks postpartum. This visit includes utilization of a validated screen for postpartum depression and, if that screen is positive, a clinical assessment and initiation of treatment (e.g. pharmacotherapy or referral for psychotherapy). In addition, this visit includes a discussion of contraception as well as supportive education on breastfeeding. For paternal care, clinical standards are gleaned from the AAP, ACOG, and USPSTF reports outlining mental health screening, reproductive health, and vaccine uptake. For infant care, standard pediatric care from the AAP and Bright Futures periodicity timeline and guidelines will be used. In addition, assignment in this arm will be given surveys at baseline, 1M, 2M, 4M, 6M, and 12M.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Digital health interventions like Baby2Home improve health literacy by providing accessible, user-friendly information and resources through mobile applications. These tools often include educational content, reminders for medical appointments, and personalized health tracking, which empower patients to manage their health more effectively.
For patients with low health literacy, such interventions are crucial as they simplify complex medical information, promote adherence to health recommendations, and facilitate timely utilization of healthcare services, ultimately leading to better health outcomes.
Mapping Digital Public Health Interventions Among Existing Digital Technologies and Internet-Based Interventions to Maintain and Improve Population Health in Practice: Protocol for a Scoping Review.A systematic review of person-centered care interventions to improve quality of facility-based delivery.The Cochrane Library review titles that are important to users of health care, a Cochrane Consumer Network project.
Mapping Digital Public Health Interventions Among Existing Digital Technologies and Internet-Based Interventions to Maintain and Improve Population Health in Practice: Protocol for a Scoping Review.A systematic review of person-centered care interventions to improve quality of facility-based delivery.The Cochrane Library review titles that are important to users of health care, a Cochrane Consumer Network project.
Find a Location
Who is running the clinical trial?
Northwestern UniversityOTHER
1,640 Previous Clinical Trials
956,930 Total Patients Enrolled
Women and Infants Hospital of Rhode IslandLead Sponsor
113 Previous Clinical Trials
39,668 Total Patients Enrolled
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,045 Previous Clinical Trials
2,730,311 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a working email address.I am 18 years old or older.My baby was born at or after 37 weeks of pregnancy.Babies who have passed away.My infant needs to be admitted to the NICU.I speak English.You have a history of intimate partner violence with your current partner, and this may exclude your partner from participating in the study.I currently have a COVID-19 infection without recovery.One or both of your parents have a serious mental illness like bipolar disorder or schizophrenia.This study is only open to people who have had their first child.
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