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Evaluation of the Efficacy of the AIM (Adult Identity Mentoring) 4 Teen Moms Program

M

Mathematica Policy Research

Status

Completed

Conditions

Pregnancy

Treatments

Behavioral: AIM 4 Teen Moms

Study type

Interventional

Funder types

Other

Identifiers

NCT01456091
MPR06549-2

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy of the AIM 4 Teen Moms program in increasing the use of long-term contraceptives, in improving adherence to contraceptives and in preventing rapid repeat pregnancies among parenting adolescents.

Full description

This study uses a randomized controlled design to evaluate the efficacy of AIM (Adult Identity Mentoring) 4 Teen Moms in reducing the incidence of rapid repeat pregnancies and associated sexual risk behavior. The AIM 4 Teen Moms program is a combination of individual and small group sessions intervention that encourages parenting young women ages 15-19 years old to delay rapid repeat pregnancies for 24 months or later. It consists of seven individual 1-hour long sessions (generally conducted in the participant's home) and two 90-minute group sessions delivered over a 12 week period. Study participants will be adolescent mothers receiving services from California's Adolescent Family Life or Cal-Learn programs in the Los Angeles County area. There will be no intervention delivered to members of the control group. This study is being conducted as part of the national Evaluation of Adolescent Pregnancy Prevention Approaches funded by the U.S. Department of Health and Human Services' Office of Adolescent Health.

Enrollment

954 patients

Sex

Female

Ages

15 to 19 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Beneficiaries of California's Adolescent Family Life or Cal-Learn programs in the Los Angeles County area
  • Female
  • 15 - 19 years old
  • Has a child between the ages 1 and 6 months at program start
  • English or Spanish speaker

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

954 participants in 2 patient groups

AIM 4 Teen Moms
Experimental group
Treatment:
Behavioral: AIM 4 Teen Moms
Control
No Intervention group

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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