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OpenTrials
Completed

NCT Number: NCT01214967

Problem Solving Education and Neonatal Intensive Care Unit (NICU) Mothers

Premature infants are born at substantial risk for poor health and developmental outcomes, which commonly include hearing and vision problems, developmental delays, and poor school performance. Premature infants of low-income families face additional social risks known to worsen these outcomes. The Institute of Medicine recognized this important public health problem in its 2006 report, Preterm Birth, which argued for the need to improve the quality of follow-up care for preterm infants discharged from the neonatal intensive care unit (NICU). The underpinning of this proposal is that maternal depression - common among families of premature infants - interferes with adherence to follow-up services, and (both through this mechanism and directly) adversely impacts child health and development. Conversely, alleviating depressive symptoms among these women represents a promising strategy to improve adherence to NICU follow-up services and to improve the outcomes of this vulnerable population.

This project aims to mitigate the adverse effects of maternal depression in this specific high-risk population by testing a theory-based, parent-directed empowerment strategy, called Problem Solving Education (PSE). In the past, similar strategies have been proven effective for improving the mood and functioning of depressed adults, and for improving adherence to medical treatment. However, they have never been tested in the setting of a parent-child relationship or among families of premature infants.

This project involves a clinical trial of PSE among 50 low-income mothers at risk for depression, who have premature infants in two Boston NICUs: Boston Medical Center and Tufts Medical Center. The investigators aim to determine the impact of PSE on maternal depressive symptoms and functioning, and adherence to child health supervision and immunization schedules, vision screening, and early intervention evaluation for babies with suspected developmental delays.

Approximately 100,000 children are born prematurely to low-income families each year. Parent-directed PSE aims to improve outcomes for these children through the prevention and/or attenuation of maternal depressive symptoms, as well as through family activation and promotion of adherence to follow-up care. If successful, PSE could also provide the cornerstone of a more generalizable empowerment strategy for families of children with chronic medical conditions.

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Key information

Conditions

Age range

15 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Boston Medical Center, Boston, Massachusetts, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Baby is ≤ 33 weeks gestational age and is expected to survive.
  • Baby qualifies to receive WIC
  • Mother is comfortable in English or Spanish.

Exclusion criteria

  • Mother has psychosis
  • Mother endorses suicidal ideation
  • Custody of baby is uncertain
  • Mother is cognitively limited, per judgment of NICU attending physician
  • Baby is critically ill, per judgment of NICU attending physician

Treatment and study plan

Problem Solving Education

Behavioral

psycho-educational intervention

Primary outcomes

  1. Maternal Depressive Symptoms

    Time frame: 6 months

Secondary outcomes

  1. Health Care Supervision Schedule for Children

    Time frame: 6 months

  2. Immunization Schedule for Children

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Boston Medical Center

Other

Collaborators

  • Tufts Medical Center

Registry information

Official study title

Empowering Low Income Mothers With Preterm Infants: a Randomized Controlled Trial

Acronym: Project Solve

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Oct 5, 2010
Registry last updated
Oct 10, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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