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OpenTrials
Completed

NCT Number: NCT00829517

Computer-Assisted Provision of Reproductive Health Care

This project seeks to demonstrate that computer kiosks in a clinic waiting room can improve access to hormonal contraception and screening for sexually transmitted infections. The study will be a randomized controlled trial which will evaluate the use of a computer kiosk module to compare the proportion of women of reproductive age who receive a prescription for hormonal contraception when computer-assisted provision of hormonal contraception is offered (intervention) to encounters when the study clinic provides standard contraceptive care (control). Subjects will be contacted approximately 3 months (range 2-4 months) after the clinic visit to complete a follow-up phone interview. The study population will include English and Spanish-speaking women ages 18-45 who seek care at this clinic. Our hypothesis is that computer-assisted provision of hormonal contraception (intervention)will increase the proportion of women of reproductive age who receive a prescription for hormonal contraception versus standard contraceptive care(control).

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of California, San Francisco, San Francisco, California, United States

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About this study

Data collection has been completed

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • women who speak English or Spanish who visit a study clinic

Exclusion criteria

  • women who do not speak English or Spanish

Treatment and study plan

computer-assisted provision of hormonal contraception

Other

a computer program available at a kiosk will offer women information about and a prescription for hormonal contraception that they can ask their clinician to sign.

Other names: Family planning kiosk

STI module

Other

computer module available at a kiosk that will encourage women to be screened for chlamydia

Other names: Chlamydia kiosk

Primary outcomes

  1. self-reported use of hormonal or more effective contraception

    Time frame: 3 months

  2. receipt of screening for sexually transmitted infection

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Registry information

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Jan 27, 2009
Registry last updated
Feb 17, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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