Skip to content

Computer-assisted Preventive Health Education for Women of Reproductive Age in Urgent Care Settings

Preventive Health Education for Women of Reproductive Age

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00177515
Enrollment
446
Registered
2005-09-15
Start date
2005-03-31
Completion date
2007-01-31
Last updated
2010-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preconception Care

Keywords

emergency contraception, folic acid, education, preventive health

Brief summary

The purpose of this study is to determine whether video doctor programs can effectively deliver preventive health messages to women of reproductive age while they wait to be seen in urgent care settings. In this study, the specific hypotheses being tested are: 1) is the video doctor program effective in improving women's knowledge about emergency contraception, and 2) is the video doctor program effective in improving women's knowledge about the importance of folate.

Detailed description

We will randomly assign participants to interact with one of two video doctor programs which have been been developed to convey messages appropriate for women of reproductive age. The video doctor is an actress (not UCSF staff) following a script that has been designed through interdisciplinary collaboration here at UCSF. These particular video programs have not been used before, but similar ones have been studied and shown to be effective by Dr. Gerber in providing patients with information about how to decrease sexual risks and the harms of alcohol and drug use. Before interacting with the video doctor program, we will assess participants baseline knowledge of the importance of peri-conception folate and the option of emergency contraception. Participants will then interact with their video doctor and be provided with a free sample of the pills their video doctor discussed. The first video doctor will educate women about the ability of folate to reduce birth defects. The discovery that peri-conception folate supplementation significantly decreases rates of neural tube defects has inspired multiple educational campaigns. However, recent work has shown that knowledge of the benefits of folate remains low, especially among minority populations. The second video doctor message will inform women of the option of emergency contraception. Emergency contraception using high doses of progesterone has been shown to reduce the risk of pregnancy to less than 2% when used up to five days after a condom failure or an episode of unprotected sex. This medication is not teratogenic and will not cause a miscarriage if used by a woman who does not know she is pregnant. Use of emergency contraception poses no long-term health risks to women and is available over-the-counter in seven European countries. Prior studies in family planning clinics , as well as the post-partum setting have shown that education about and advance provision of emergency contraceptive pills can increase knowledge and appropriate use of these pills, without adversely affecting sexual risk taking or other health behaviors. However, knowledge of emergency contraception remains limited, leading some to call it America's best kept secret. Participants will be contacted by phone six months after interacting with the video doctor and asked to provide information about their use of folate and/or emergency contraception. One year after interacting with the video doctor participants will be contacted again and asked to provide further information about their use of folate and/or emergency contraception.

Interventions

BEHAVIORALvideo doctor, computer module

computerized counseling about emergency contraception and peri-conception folate

Sponsors

University of California, San Francisco
CollaboratorOTHER
University of Pittsburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-45 year old English-speaking women

Exclusion criteria

* current pregnancy * history of tubal ligation * hysterectomy * partner with a vasectomy * no sex with men * will not be able to be reached by telephone in 6 months

Design outcomes

Primary

MeasureTime frame
Use of Emergency Contraception7 months
Use of Folate supplements7 months

Secondary

MeasureTime frame
Access to Emergency Contraception at home7 months
Knowledge of emergency contraception7 months
Knowledge of the benefits of folate supplementation7 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026