UCSF College Health Study on Contraceptive Training and Education at Community Colleges

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Active, not recruiting

Conditions

Contraception

Treatments

Behavioral: Placebo Nutrition Education
Behavioral: Contraceptive Training and Education

Study type

Interventional

Funder types

Other

Identifiers

NCT03519685
A125604

Details and patient eligibility

About

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.

Full description

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.

Enrollment

2,086 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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:

  • Female;
  • 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.

Exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

2,086 participants in 2 patient groups, including a placebo group

Contraceptive Training and Education
Experimental group
Description:
Colleges assigned to this arm receive a one-day UCSF Continuing Medical Education (CME # MMC18087) accredited training on contraceptives and technical assistance. The training is for staff at the student health center and local health centers where they refer for contraceptive services. Students attending colleges assigned to this arm receive education about contraceptive methods and how to access services.
Treatment:
Behavioral: Contraceptive Training and Education
Nutrition Education
Placebo Comparator group
Description:
Students attending colleges assigned to this arm receive nutrition education about the impacts of sugar on health.
Treatment:
Behavioral: Placebo Nutrition Education

Trial contacts and locations

1

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Central trial contact

Cynthia C. Harper, PhD

Data sourced from clinicaltrials.gov

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