MedPath

Reducing Symptoms of Depression in Low-Income Mothers

Phase 2
Completed
Conditions
Depression
Interventions
Behavioral: Attention control/usual care
Behavioral: Modified Interpersonal Therapy
Registration Number
NCT00074789
Lead Sponsor
University of North Carolina, Chapel Hill
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
226
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
Read More
Exclusion Criteria
  • Regular use of psychotropic medication
  • Regular use of psychotherapy or drug/alcohol treatment
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
2Attention control/usual careParticipants will receive attention control/usual care for 26 weeks
1Modified Interpersonal TherapyParticipants will receive home-based interpersonal depression treatment for 26 weeks
Primary Outcome Measures
NameTimeMethod
Level of depressive symptomsMeasured at Week 26
Secondary Outcome Measures
NameTimeMethod
Mother child interactionsMeasured at Week 26

Trial Locations

Locations (6)

P.E.A.C.E, Inc. Early Head Start

🇺🇸

Syracuse, New York, United States

Asheville City Schools Preschool-Early Head Start Program

🇺🇸

Asheville, North Carolina, United States

United Child Development Services, Inc. Early Head Start

🇺🇸

Greensboro, North Carolina, United States

W.A.G.E.S., Inc. Early Head Start Program

🇺🇸

Goldsboro, North Carolina, United States

Chapel Hill Training Outreach Project, Inc. Early Head Start

🇺🇸

Chapel Hill, North Carolina, United States

University of North Carolina, Chapel Hill

🇺🇸

Chapel Hill, North Carolina, United States

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