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Reducing Symptoms of Depression in Low-Income Mothers

Reducing Depressive Symptoms in Low-Income Mothers

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00074789
Enrollment
226
Registered
2003-12-22
Start date
2003-06-30
Completion date
2009-01-31
Last updated
2013-06-21

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

Conditions

Depression

Keywords

Early Head Start Program

Brief summary

This study will test the effectiveness of a short-term intervention in treating depressed young mothers with young children enrolled in Early Head Start Programs.

Detailed description

Limited resources, poor social support, and complex life problems contribute to the high prevalence and severity of depressive symptoms in low-income mothers. As depressive symptoms persist, they often rob young mothers of the energy they need for school, job training, and positive interaction with their children, which can negatively affect a child's language acquisition, intellectual development, and social conduct. This study will design and implement a home-based treatment to help young mothers manage their depressive symptoms, increase their social support, manage or resolve life issues, and effectively parent their infant or toddler through the use of EHS resources. Mothers will be randomly assigned to receive either home-based interpersonal depression treatment or an attention control/usual care condition for 26 weeks. Assessments will be made at study start and Weeks 14, 22, and 26. Depression scales, interviews, and analyses of videotaped mother-child interactions will be used to assess participants. Stress, social support, and use of EHS services will be assessed.

Interventions

BEHAVIORALModified Interpersonal Therapy

Psychiatric mental health nurses will meet with participants 10 times, an hour each time, over a period of 14 weeks. The nurses will continue to work with the mothers over the next 8 weeks by phone, conducting 5 fifteen minute phone sessions.

BEHAVIORALAttention control/usual care

Participants will receive the usual care for depression.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Score of 16 or higher on the Center for Epidemiological Studies Depression (CES-D) Scale * Child who is 6 weeks to 30 months old * Child who is enrolled in an Early Head Start program

Exclusion criteria

* Regular use of psychotropic medication * Regular use of psychotherapy or drug/alcohol treatment

Design outcomes

Primary

MeasureTime frame
Level of depressive symptomsMeasured at Week 26

Secondary

MeasureTime frame
Mother child interactionsMeasured at Week 26

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026