Study Details

Citation

Covington, R., et al. Interim Impacts of the AIM 4 Teen Moms Program. Mathematica Policy Research, Princeton, NJ: 2015.

Covington, Reginald D., Dara Lee Luca, Jennifer Manlove, and Kate Welti. “Final Impacts of AIM 4 Teen Moms.” Washington, DC: U.S. Department of Health and Human Services, Office of Adolescent Health, February 2017.

Program or Component Study?
Program
Program or Component Name

AIM 4 Teen Moms (AIM4TM)

Show Evidence of Effectiveness
Yes
Study Rating and Explanation
Moderate

Random assignment study with high attrition that that did not meet the criteria for a high rating but met all criteria for a moderate rating; findings show a positive, statistically significant impact for at least one behavioral outcome

Program Information

Program Type
Sexual health education
Program Length
Fewer than 10 sessions

Evaluation Setting

Evaluation Setting
Community-based organization
Home-based

Study Sample

Average Age Group
14 to 17
Majority Racial/Ethnic Group
Hispanic or Latinx of any race
Gender
Young women

Research Design

Assignment Method
Randomized controlled trial
Sample Size

800

Number of Follow-Ups

1

Year of Last Data Collection
2014

Study Findings

Result Number Partners
Indeterminate evidence
Result Sexual Activity
Indeterminate evidence
Result Contraceptive
Potentially favorable evidence
Result Pregnancy
Indeterminate evidence
Reviewed Studies
Moderate-Quality Randomized Trial
Protocol Version
Version 5.0
Details

The program was evaluated in a randomized controlled trial involving low-income adolescent mothers in Los Angeles County. Participants were randomly assigned to either an intervention group receiving AIM 4 Teen Moms (AIM4TM) or a control group that was not offered the program but that had access to other services for teen mothers in their communities. Outcomes were measured 12 and 24 months after participants enrolled in the study.

The study found that 12 months after enrollment, adolescent mothers in the intervention group were less likely to report having had sex without any effective contraceptive method in the past three months (odds ratio = 0.72, confidence interval = 0.61 to 0.85). This effect was not sustained 24 months after enrollment: adolescent mothers in the intervention group were no less likely than their counterparts in the control group to report having had sex without any effective contraceptive method in the past three months (odds ratio = 1.19).

Twelve and 24 months after enrollment, the study found no statistically significant program impacts on having had sexual intercourse in the past three months, the number of sexual partners in the past 12 months, or on having sex without using a condom or specific forms or birth control methods such as birth control pills, an implant, any LARC method, an IUD, the shot, the patch, or the ring, in the past three months. At the follow-up that occurred 24 months after enrollment, the study also found no evidence of statistically significant program impacts on repeat pregnancy, the number of pregnancies since birth of first child, and repeat pregnancy resulting in a new birth.

Program impacts were also examined on measures of exposure to information about effective contraception, school or work engagement, support for safe sex, and intentions to avoid unprotected sexual activity. Findings for these outcomes were not considered for the review because they fell outside the scope of the review.

Effect Sizes
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NA = Not available. This means the authors did not report the information in the manuscripts associated with the studies we reviewed.

a This information was not available whenever authors did not report information for the treatment and comparison groups separately on outcome means, standard deviations, and/or sample sizes.

b Authors reported that the program effect (impact) estimate is statistically significant with a p-value of less than 0.05 based on a two-tailed test.

c For some outcomes, having less of that outcome is favorable. In those cases, an effect with a negative sign is favorable to the treatment group (that is, the treatment group had a more favorable outcome than the comparison group, on average).

d An effect shows credibly estimated, statistically significant evidence whenever it has a p-value of less than 0.05 based on a two-tailed test, includes the appropriate adjustment for clustering (if applicable), and it is not based on an endogenous subgroup.