Computer-Assisted Provision of Reproductive Health Care
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ClinicalTrials.gov Identifier: NCT00829517 |
Recruitment Status
:
Completed
First Posted
: January 27, 2009
Last Update Posted
: February 17, 2012
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Contraception Sexually Transmitted Diseases | Other: computer-assisted provision of hormonal contraception Other: STI module | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 814 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Outcomes Assessor) |
Primary Purpose: | Health Services Research |
Official Title: | Computer-Assisted Provision of Reproductive Health Care |
Study Start Date : | January 2011 |
Actual Primary Completion Date : | November 2011 |
Actual Study Completion Date : | November 2011 |
Arm | Intervention/treatment |
---|---|
Active Comparator: STI kiosk
computer-assisted provision of screening for chlamydia
|
Other: STI module
computer module available at a kiosk that will encourage women to be screened for chlamydia
Other Name: Chlamydia kiosk
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Experimental: contraceptive kiosk
computer-assisted provision of hormonal contraception
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Other: computer-assisted provision of hormonal contraception
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 Name: Family planning kiosk
|
- self-reported use of hormonal or more effective contraception [ Time Frame: 3 months ]
- receipt of screening for sexually transmitted infection [ Time Frame: 3 months ]

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Ages Eligible for Study: | 18 Years to 45 Years (Adult) |
Sexes Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- women who speak English or Spanish who visit a study clinic
Exclusion Criteria:
- women who do not speak English or Spanish

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00829517
United States, California | |
University of California, San Francisco | |
San Francisco, California, United States, 94122 | |
United States, Pennsylvania | |
UPMC | |
Pittsburgh, Pennsylvania, United States, 15213 |
Principal Investigator: | Eleanor B Schwarz, MD, MS | University of Pittsburgh |
Responsible Party: | Eleanor Bimla Schwarz, Associate Professor of Medicine, University of Pittsburgh |
ClinicalTrials.gov Identifier: | NCT00829517 History of Changes |
Other Study ID Numbers: |
SFP2-8 |
First Posted: | January 27, 2009 Key Record Dates |
Last Update Posted: | February 17, 2012 |
Last Verified: | February 2012 |
Keywords provided by Eleanor Bimla Schwarz, University of Pittsburgh:
Contraception sexually transmitted diseases |
Additional relevant MeSH terms:
Sexually Transmitted Diseases Infection Virus Diseases Genital Diseases, Male Genital Diseases, Female |