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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
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Contraception focused on measuring Contraception, sexually transmitted diseases

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

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

First Posted
January 23, 2009
Last Updated
February 15, 2012
Sponsor
University of Pittsburgh
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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

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Computer-Assisted Provision of Reproductive Health Care

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