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临床试验/NCT03519685
NCT03519685已完成不适用

UCSF College Health Study: A Cluster Randomized Trial on Contraceptive Training and Education at Community Colleges

University of California, San Francisco2 个研究点 分布在 1 个国家目标入组 2,086 人开始时间: 2018年4月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
2,086
试验地点
2
主要终点
Change in student knowledge of full range of contraceptive methods (questionnaire)

研究概览

简要总结

The purpose of this study is to measure whether a training and education intervention for clinic staff and young women aged 18-25 on contraceptive methods, including intrauterine devices (IUDs) and the implant, will result in greater contraceptive knowledge and access among students in community colleges.

详细描述

In the US, young women aged 18-25 years have limited knowledge of contraception or pregnancy risks and often experience challenges in accessing reproductive health care. They have little familiarity with the full range of contraceptives, particularly long-acting reversible contraception (LARC) including the IUD and implant. This campus-level, multiple component intervention provides evidence-based contraceptive training and education to clinic staff and students in this age group attending community colleges in California and Texas.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • This study involves two groups of human subjects: students at 28 community colleges and staff at the student health center and referral clinics.
  • Students must be:
  • Age 18-25;
  • Speaks English;
  • Sexually active (vaginal sex with a male partner) in the last year;
  • Not currently pregnant;
  • Does not want to become pregnant in the next 12 months;
  • At risk of pregnancy (including not sterilized);
  • Enrolled in the current term at the participating community college;
  • First-time college students, meaning no college enrollment prior to the current academic year; and
  • Willing to be contacted by email and telephone over the next 12 months.
  • Clinic staff must:
  • Be employed by a participating clinic; and
  • Offer clinical care, counseling or education for contraception at the clinic.
  • For colleges to be eligible to be study sites, they must:
  • Be an accredited community college;
  • Not share health center staff with a participating college site;
  • Have no active LARC intervention; and
  • Enroll students ages 18-25 years.

排除标准

  • Students and clinic staff will be excluded if they do not meet the inclusion criteria.

结局指标

主要结局

Change in student knowledge of full range of contraceptive methods (questionnaire)

时间窗: Baseline, immediate post educational intervention session

The outcome is measured by whether student knows of reversible methods including male condom, female condom, oral contraceptive pill, transdermal patch, vaginal ring, Depo-provera injectable, intrauterine device, subdermal implant, and emergency contraception.

次要结局

  • Change in student access to contraceptive services over 12 months, measured as whether student knows of or visited health services for contraceptives (questionnaire)(Baseline, 12 months)
  • Change in willingness to use long-acting reversible contraception (LARC) (questionnaire)(Baseline, immediate post educational intervention session)
  • Change in LARC use over 12 months (questionnaire)(Baseline, 12 months)
  • Dual condom use at last sex, measured by student report of condom use together with another method of birth control at last vaginal sex (questionnaire)(Baseline, 6 months, 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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