Examining the impact of a pediatric sleep app on infant sleep and maternal mental health
Association of Digital Aid Use With Infant Sleep and Maternal Mental Health
This study tests whether using the Huckleberry sleep app can help babies sleep better and improve the mental health of their mothers, especially for those on Medicaid.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 120 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | University of Massachusetts, Worcester Academic / other |
| Locations | 1 site (Worcester, Massachusetts) |
| Trial ID | NCT06593236 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the effects of the Huckleberry app, designed to guide pediatric sleep, on both infant sleep patterns and maternal mental health, particularly within the Medicaid population. By analyzing user experiences and outcomes, the study aims to provide insights into how digital tools can address common sleep issues in infants and support mothers' mental well-being. Additionally, it seeks to evaluate improvements in Medicaid Accountable Care Organizations' goals through stakeholder interviews.
Who should consider this trial
Good fit: Ideal candidates are mothers aged 18 or older with infants between 0-12 months who receive healthcare through UMass Memorial Health and are part of the Medicaid ACO population.
Not a fit: Patients who lack internet access, do not understand English, or have infants in DCF custody or in the NICU may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance infant sleep quality and improve maternal mental health, leading to better overall family well-being.
How similar studies have performed: While the use of digital aids for infant sleep is a growing field, this specific approach using the Huckleberry app is relatively novel and has not been extensively tested in similar studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Is at least 18 years old * Has a child between the age of 0-12 months * Receives healthcare through UMass Memorial Health * Is a part of the Medicaid Accountable Care Organizations (ACO) population Exclusion Criteria: * Lacks capacity to consent * Does not understand English * Does not have internet access on their smartphone or at home * If the infant is in Department of Children and Families (DCF) custody or is admitted into the Neonatal Intensive Care Unit (NICU)
Where this trial is running
Worcester, Massachusetts
- UMass Chan Medical School — Worcester, Massachusetts, United States (Recruiting)
Study contacts
- Principal investigator: Nish Fahey, DO — Assistant Professor
- Study coordinator: Nisha Fahey, DO
- Email: Nisha.Fahey@umassmed.edu
- Phone: 774-455-6677
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.