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Depression Prevention Program for American Indian Adolescents During and After Pregnancy

Not Applicable
Completed
Conditions
Depression
Pregnancy
Interventions
Behavioral: "Living in Harmony" depression prevention program
Behavioral: Depression-prevention education and support
Registration Number
NCT00183547
Lead Sponsor
Johns Hopkins University
Brief Summary

This study will determine the effectiveness of the "Living in Harmony" depression prevention program in preventing depressive symptoms among pregnant American Indian adolescents during pregnancy and after giving birth.

Detailed Description

Pregnancy among reservation-based American Indian adolescents has become increasingly common. Numerous psychosocial and environmental factors have put this population at high risk for pregnancy-related depression. Depression during pregnancy and after giving birth is associated with reduced quality of life for both young mothers and their children. Many reservations lack mental health services; therefore, an inexpensive intervention is needed to prevent depressive symptoms among pregnant adolescents who live on reservations.

The duration of this study will vary for each participant, depending on the time of study entry. Participants will be randomly assigned to receive weekly sessions of either the "Living in Harmony" program, consisting of cognitive behavioral therapy (CBT), culturally-relevant education, and support; or general depression-prevention education and support. Participants' depressive symptoms will be assessed at study entry, at 4, 12, and 24 weeks after giving birth, and study completion. Interviews and self-report scales will be used to assess participants.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
45
Inclusion Criteria
  • At 28th week or earlier of pregnancy
  • Center for Epidemiologic Studies-Depression Scale (CES-D) score of 16 or higher
  • Identified (by others and by self) as an American Indian
  • Currently live on an American Indian reservation
  • Parent or guardian willing to give consent, if applicable
  • Willing and able to comply with all study requirements
Exclusion Criteria
  • Diagnosis of major depressive disorder
  • Current psychiatric disorder or condition requiring intervention or treatment
  • Current participation in another mental or behavioral health study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1"Living in Harmony" depression prevention program"Living in Harmony" depression prevention program
2Depression-prevention education and supportDepression-prevention education and support
Primary Outcome Measures
NameTimeMethod
Postpartum depressionup to 24 weeks postpartum
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Johns Hopkins Center for American Indian Health

🇺🇸

Baltimore, Maryland, United States

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