Improving Preschool Outcomes by Addressing Maternal Depression in Head Start
Study Details
Study Description
Brief Summary
This research study is a community-based efficacy trial (n=388) of a stepped-care model intervention to strengthen the capacity of Head Start to address parental depression and related adversities. Head Start mothers with symptoms of depressed mood or anhedonia, and their Head Start children, are enrolled across 12 Head Start centers.
The research study aims to improve developmental outcomes for Head Start children by delivering stepped care intervention that incorporates depression prevention and linkage to formal mental health care to mothers. Mothers with low baseline depressive symptoms are offered a problem-solving intervention while mothers with greater symptoms are offered engagement sessions to link them to formal mental health services. At each problem solving session participant's symptoms are assessed and if the symptoms meet pre-specified 'step-up' criteria, they are converted to Engagement sessions.
Over 12-months, the intervention's effect will be assessed on a series of outcome measures for mothers; mechanisms by which maternal depression is theorized to impact young children; and child outcomes.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Stepped-care intervention (SCI) group In the SCI group, mothers with low baseline depressive symptoms are offered the problem-solving education (PSE) prevention intervention, and mothers with greater depressive symptoms are offered Engagement Sessions. |
Behavioral: Problem-solving education (PSE)
PSE will be offered to mothers with low baseline depressive symptoms (the first, preventive step of the SCI). PSE participants will have their symptoms assessed at each session and will convert to Engagement Sessions if they meet pre-specified 'step up' criteria.
Behavioral: Engagement sessions
Engagement sessions will be offered to mothers with greater depressive symptoms to link them to formal mental health services (the second, referral step of the SCI)
|
| Active Comparator: Usual care control group Families in the control group will receive usual Head Start services. |
Behavioral: Usual care
Normal services provided children and their mothers in Head Start
|
Outcome Measures
Primary Outcome Measures
- Change in incident rates of moderate to severe maternal depressive symptoms based on the QIDS [Baseline, 2, 4, 6, 8, 10, 12 months follow-up]
The Quick Inventory of Depressive Symptoms (QIDS) will be used to assess the incidence of moderate to severe depressive symptom episodes, as defined by a QIDS score ≥ 11. The QIDS is a 16 item self-administered instrument with potential responses for each item of 0 to 3. Higher scores are associated with greater depressive symptoms.
- Change in the mean maternal depressive symptoms based on the QIDS [Baseline, 2, 4, 6, 8, 10, 12 months follow-up]
The Quick Inventory of Depressive Symptoms will be used to assess depressive symptoms. The QIDS is a 16 item self-administered instrument with potential responses for each item of 0 to 3. Higher scores are associated with greater depressive symptoms. The mean QIDS scores will be calculated for the baseline and each follow up period.
Secondary Outcome Measures
- Rate of participants engaged with care based on 1 or more psycho/pharmacotherapy visits or psychiatric medication prescription [Baseline, 2, 4, 6, 8, 10, 12 months follow-up]
The investigators have adapted the services section of the Collaborative Psychiatric Epidemiology Surveys, operationalized into engagement with care. This will be defined as ≥ 1 visit for psychotherapy or pharmacotherapy with a behavioral health specialist (social worker, psychologist, psychiatrist, psychiatric nurse); or a prescription for psychiatric medication from any medical practitioner.
- Rate of participants retained in care based on 4 or more psycho/pharmacotherapy visits or psychiatric medication prescription [2, 4, 6, 8, 10, 12 months]
The investigators have adapted the services section of the Collaborative Psychiatric Epidemiology Surveys, operationalized into retention in care. This will be defined as ≥ 4 visit for psychotherapy or pharmacotherapy with a behavioral health specialist (social worker, psychologist, psychiatrist, psychiatric nurse); or a prescription for psychiatric medication from any medical practitioner.
- Rate of participants who received evidence-based care defined by psychotherapy or antidepressant medication prescription [2, 4, 6, 8, 10, 12 months]
The investigators have adapted the services section of the Collaborative Psychiatric Epidemiology Surveys, operationalized into evidence-based care reflecting either psychotherapy or antidepressant medication.
- Rate of participants who received primary-care based services [2, 4, 6, 8, 10, 12 months]
The investigators have adapted the services section of the Collaborative Psychiatric Epidemiology Surveys, operationalized into primary care-based services.
- Burden of illness for depression [baseline; 6, 12 months]
The Individual Burden of Illness Index for Depression (IBI-D) is a valid and reliable quality of life (QoL) scale, calculated as a composite of the QIDS, the QoL Enjoyment and Satisfaction Questionnaire, and the Work and Social Adjustment Scale
- Child absenteeism from Head Start [baseline; 6, 12 months]
Head Start centers will furnish us with monthly absentee rates for all families that provide explicit permission. These will be analyzed as count data against day of eligible attendance.
- Caregiver-Teacher Report Form [baseline; 6, 12 months]
This valid and reliable scale will be filled out by Head Start teachers. It measures emotional reactivity, anxiety/depression, somatic complaints, emotional withdrawal, attention problems, and aggressive behavior.
- Social Skills Improvement System - Rating Scales [baseline; 6, 12 months]
This valid and reliable scale will be filled out by Head Start teachers. It assesses social skills and problem behaviors for children at risk of interpersonal difficulties.
- Bracken School Readiness Assessment [baseline; 6, 12 months]
This scale assesses 85 foundational concepts, including colors, letters, numbers, size/ comparison, and shapes. Assess effect of intervention on child cognitive functioning and school readiness.
- Perceived Stress [baseline, 4, 8, 12 months]
Assess with The Perceived Stress Scale, domains of which include unpredictability, lack of control, burden overload, and stressful circumstances.
- Behavioral Activation for Depression [baseline, 4, 8, 12 months]
Assess with The Behavioral Activation for Depression Scale (BADS) includes four affective and functional dimensions: activation, avoidance/rumination, work/school impairment, and social impairment.
- Coping Strategies [baseline, 4, 8, 12 months]
Assess with The Brief COPE (Coping Orientation to Problems) which measures 14 different adaptive and problematic coping styles. Will also use problem-focused and avoidant subscales.
- Parent-Child Interaction [baseline, 6, 12 months]
Assess with The Dyadic Parent-Child Interaction Coding System (4th Edition).
- Family Conflict [Baseline, 6, 12 months]
Assess with The 80-item Conflicts and Problem-Solving Scale. Likert scales rate aspects of family conflict known to affect children: 1) number of major and minor conflicts in the past year; 2) family disagreement in 21 areas; 3) frequency of 13 conflict resolution strategies; 4) frequency of 44 conflict tactics.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Mother of a 0 to 5-year-old Head Start child, whose Head Start services will continue for at least 12 months following randomization
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Mother endorses depressed mood or anhedonia on PHQ-9 (Patient Health Questionnaire-9)
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Mother speaks English or Spanish
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Mother is Medicaid beneficiary
Exclusion Criteria:
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Mother with suicidal ideation
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Mother with cognitive limitation
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Boston Medical Center
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Investigators
- Principal Investigator: Emily Feinberg, ScD CPNP, BU School of Medicine, Pediatrics and BUSPH
- Principal Investigator: Michael Silverstein, MD, Brown University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- H-39166
- 1R01HD092456-01A1