Clinical Trial: Reducing Symptoms of Depression in Low-Income Mothers

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to test the effectiveness of a short-term intervention in treating depressed young mothers with young children enrolled in Early Head Start (EHS) Programs.

Condition Treatment or Intervention Phase
Depression
 Procedure: Modified Interpersonal Therapy
Phase II

MedlinePlus related topics:  Depression

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study

Official Title: Reducing Depressive Symptoms in Low-Income Mothers

Further Study Details: 

Expected Total Enrollment:  226

Study start: June 2003;  Expected completion: May 2008

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.

Eligibility

Ages Eligible for Study:  15 Years and above,  Genders Eligible for Study:  Female

Criteria

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

Location and Contact Information


New York
      P.E.A.C.E, Inc. Early Head Start, Syracuse,  New York,  13203,  United States; Recruiting
Regina Canuso, MSN  315-470-3370  Ext. 318    rcanuso@peace-caa.org 
Coleen Meehan  315-470-3300    cmeehan@peace-caa.org 
Regina Canuso, RN, MSN,  Sub-Investigator

North Carolina
      Chapel Hill Training Outreach Project, Inc. Early Head Start, Chapel Hill,  North Carolina,  27514,  United States; Recruiting
Angela Wilcox  919-490-5577  Ext. 242    awilcox@intrex.net 
Ennis Baker  919-490-5577    edellea@intrex.net 

      Asheville City Schools Preschool-Early Head Start Program, Asheville,  North Carolina,  28806,  United States; Recruiting
Edel Seay  828-255-5423    edel.seay@asheville.k12.nc.us 
Malvary Gamble  828-255-5423    malvary.gamble@asheville.k12nc.us 

      United Child Development Services, Inc. Early Head Start, Greensboro,  North Carolina,  27406,  United States; Recruiting
Glenda Welch  336-378-3300    glenda@ucds.net 

      McDowell County Borad of Education Early Head Start, Marion,  North Carolina,  28752,  United States; Not yet recruiting
Carol Yancey  828-652-3229    cyancey@mcdowell.k12nc.us 

More Information

Study ID Numbers:  MH65524-01A2; HILDA
Record last reviewed:  March 2005
Last Updated:  March 24, 2005
Record first received:  December 19, 2003
ClinicalTrials.gov Identifier:  NCT00074789
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005