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Preventing Maternal Depression In Head Start

Preventing Maternal Depression In Head Start

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01298804
Enrollment
230
Registered
2011-02-18
Start date
2011-02-28
Completion date
2016-07-31
Last updated
2016-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Brief summary

Maternal depression disproportionately affects low-income and minority women, and has profound negative impacts on their children. The investigators are conducting a randomized trial of a systems approach to identify mothers at risk for depression in Head Start - a federally funded early learning program for children of low-income families - and to provide an on-site intervention to prevent or alleviate depressive symptoms; improve functioning; and, where appropriate, proactively link mothers to more definitive mental health services.

Detailed description

This study is one component of a series of studies that aims to develop a comprehensive system of maternal depression prevention and management within Head Start. In our March 2014 review of the CT.gov protocol, we synchronized it with our institution's IRB protocol, which had been modified based on how the individual studies within this series relate to one another. Specifically, the original IRB protocol combined two studies into one: a 'main' depression prevention trial (n=230, R01MH091871), and a small adjunct pilot aimed at referring those with symptoms of major depression to further care (n=60). Thus, the original CT.gov protocol included subjects both at risk for depression and with symptoms consistent with major depression. When the latter pilot study subsequently received external funding, we separated the two studies into two IRB protocols, and thus have adjusted our CT.gov protocol to the appropriate sample size of 230, and indicated symptoms of major depression as an exclusion criterion for the prevention trial. Because Major Depressive Episode was inadvertently listed as a primary outcome measure for the prevention trial (and PTSD and Anxiety as secondary outcome measures), we have removed them as such and listed it under 'other' outcomes, thereby aligning the CT.gov protocol with the statistical analysis plan of the original grant application and IRB protocol. Lastly, we corrected administrative errors in the study's projected end date and masking design.

Interventions

BEHAVIORALProblem Solving Education and Activated Referral to Care

The intervention represents an integrated identification and intervention system based on the evidence-based construct of screening, brief intervention, and referral to treatment (SBIRT). Within the comprehensive case management services of Head Start, eligible women will be randomized to receive either usual care or the Head Start-based intervention. In our intervention, mothers at risk for depression will receive a problem-solving intervention; depression symptom monitoring; and an Activated referral to more definitive services for those who have worsening symptoms over time.

Sponsors

Head Start and Early Head Start Programs in Action for Boston Community Development Incorporated
CollaboratorUNKNOWN
Boston Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Family enrolled in Head Start, and child expected to attend Head Start activities for at least 6 months of the 12-month follow-up period. * Family without imminent plans to relocate * Mother is comfortable in English or Spanish. * Parent/guardian who has a child that attends Head Start * Child attending Head Start and is between the ages 0-5 * Screen positive to 2-question depression screener (PHQ2), or have a past history of depression * Ability to provide informed consent. * Not suicidal

Exclusion criteria

* High suicidal ideation * Cognitive limitation * Psychosis * No known risks for depression * Symptoms reflecting major depressive episode

Design outcomes

Primary

MeasureTime frameDescription
Problem Solving Skills6 monthsSocial Problem Solving Inventory
Depression Symptoms2 monthsQIDS

Secondary

MeasureTime frameDescription
Parent functioning/stress6 monthsParenting Stress Index; Perceived Stress Index
Head Start attendance12 monthsHead Start records, analyzed as monthly absence rates
Social functioning6 monthsSocial Adjustment Scale- Self-report
Receipt of Mental Health Services12 months
Child Behavior6 monthsTeacher Version of Social Skills Rating System

Other

MeasureTime frameDescription
Post Traumatic Stress Disorder12 monthsSCID Interview
Major Depressive Episode12 monthsSCID Interview
Anxiety12 monthsSCID Interview

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026