Computer-Assisted Provision of Reproductive Health Care
Primary Purpose
Contraception, Sexually Transmitted Diseases
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
computer-assisted provision of hormonal contraception
STI module
Sponsored by
About this trial
This is an interventional health services research trial for Contraception focused on measuring Contraception, sexually transmitted diseases
Eligibility Criteria
Inclusion Criteria:
- women who speak English or Spanish who visit a study clinic
Exclusion Criteria:
- women who do not speak English or Spanish
Sites / Locations
- University of California, San Francisco
- UPMC
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
STI kiosk
contraceptive kiosk
Arm Description
computer-assisted provision of screening for chlamydia
computer-assisted provision of hormonal contraception
Outcomes
Primary Outcome Measures
self-reported use of hormonal or more effective contraception
receipt of screening for sexually transmitted infection
Secondary Outcome Measures
Full Information
NCT ID
NCT00829517
First Posted
January 23, 2009
Last Updated
February 15, 2012
Sponsor
University of Pittsburgh
1. Study Identification
Unique Protocol Identification Number
NCT00829517
Brief Title
Computer-Assisted Provision of Reproductive Health Care
Official Title
Computer-Assisted Provision of Reproductive Health Care
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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).
Detailed Description
Data collection has been completed
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Contraception, Sexually Transmitted Diseases
Keywords
Contraception, sexually transmitted diseases
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
814 (Actual)
8. Arms, Groups, and Interventions
Arm Title
STI kiosk
Arm Type
Active Comparator
Arm Description
computer-assisted provision of screening for chlamydia
Arm Title
contraceptive kiosk
Arm Type
Experimental
Arm Description
computer-assisted provision of hormonal contraception
Intervention Type
Other
Intervention Name(s)
computer-assisted provision of hormonal contraception
Other Intervention Name(s)
Family planning kiosk
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
STI module
Other Intervention Name(s)
Chlamydia kiosk
Intervention Description
computer module available at a kiosk that will encourage women to be screened for chlamydia
Primary Outcome Measure Information:
Title
self-reported use of hormonal or more effective contraception
Time Frame
3 months
Title
receipt of screening for sexually transmitted infection
Time Frame
3 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
women who speak English or Spanish who visit a study clinic
Exclusion Criteria:
women who do not speak English or Spanish
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eleanor B Schwarz, MD, MS
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94122
Country
United States
Facility Name
UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Computer-Assisted Provision of Reproductive Health Care
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