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Clinical Trial
. 2001 Jan;155(1):73-9.
doi: 10.1001/archpedi.155.1.73.

Randomized controlled trial of a safer sex intervention for high-risk adolescent girls

Affiliations
Clinical Trial

Randomized controlled trial of a safer sex intervention for high-risk adolescent girls

L A Shrier et al. Arch Pediatr Adolesc Med. 2001 Jan.

Abstract

Objective: To determine the effect of an individualized safer sex intervention on condom use and recurrent sexually transmitted disease (STD) among female adolescents diagnosed as having an STD.

Design: Randomized controlled trial.

Setting: Urban children's hospital adolescent clinic and inpatient service.

Participants: One hundred twenty-three adolescents with cervicitis or pelvic inflammatory disease.

Intervention: Participants completed a questionnaire and then were randomized to receive standard STD education or to watch a videotape and have an individualized intervention session. Follow-up questionnaires were completed at 1, 3, 6, and 12 months. Intervention participants met with an educator at 1, 3, and 6 months to discuss interim sexual history and review the intervention.

Main outcome measures: Change in self-reported condom use and recurrence of STD. Other self-reported behaviors, sexual risk knowledge, attitudes toward condoms, and condom use negotiation skills were also assessed.

Results: At 1 month, compared with control participants, intervention participants had increased sexual risk knowledge and more positive attitudes toward condoms and tended to use condoms more with a nonmain partner. At 6 months, fewer intervention participants than controls had sex with a nonmain sexual partner in the previous 6 months. At 12 months, intervention participants were less likely to have a current main partner and had a lower rate of recurrent STD than controls, but these differences were not significant.

Conclusions: This individualized safer sex intervention may improve condom use and decrease the number of partners among adolescent girls who have had an STD. Studies with larger samples are needed to determine definitive intervention effects on recurrent STD in this high-risk population.

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