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Interpersonal Therapy-Based Treatment to Prevent Postpartum Depression in Adolescent Mothers

Women and Infants Hospital of Rhode Island logo

Women and Infants Hospital of Rhode Island

Status

Completed

Conditions

Depression

Treatments

Behavioral: Interpersonal therapy-based treatment
Behavioral: Standard care

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00436150
DSIR 84-CTP
R34MH077588 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study will aim to prevent postpartum depression in pregnant teenagers through an interpersonal therapy-based program.

Full description

Postpartum depression is believed to be one of the most common complications after pregnancy. This type of depression often occurs within the first year after the baby is born and is most likely caused by dramatic changes in hormone levels after pregnancy. Pregnant teenagers are even more at risk for experiencing complications throughout pregnancy and parenting difficulties after delivery. Minimal research has been done on preventive ways to reduce postpartum depression in teenagers. Therefore, this study will evaluate the effectiveness of an interpersonal therapy-based program at preventing postpartum depression in financially disadvantaged pregnant teenagers.

Participants will first undergo a 15-minute interview about their background and emotions. Participants will undergo a second interview and then be randomly assigned to receive either interpersonal therapy-based treatment or standard care. Participants assigned to receive interpersonal therapy-based treatment will focus on the psychological aspects of pregnancy and factors that may play a role in the development of postpartum depression in teenage mothers, such as poor social support, role transitions, and life stressors. Participants assigned to receive standard care will focus more on the health issues associated with pregnancy and postpartum. Both groups will attend weekly 1-hour sessions for 5 weeks. Homework may be assigned to review topics discussed, and all participants will receive the book Baby Basics. Following treatment, participants will meet with researchers again when they are 34 to 36 weeks pregnant; in the hospital after the baby is born; and 6, 12, and 24 weeks after the baby is born.

Enrollment

106 patients

Sex

Female

Ages

12 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Less than 24 weeks pregnant
  • Not currently being treated for depression
  • Speaks and reads English fluently

Exclusion criteria

  • Currently receiving mental health services from a health care provider
  • Meets DSM-IV criteria for an affective disorder, substance use disorder, or psychosis

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

106 participants in 2 patient groups

A
Experimental group
Description:
Participants will receive interpersonal therapy-based treatment
Treatment:
Behavioral: Interpersonal therapy-based treatment
B
Active Comparator group
Description:
Participants will receive standard care
Treatment:
Behavioral: Standard care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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