Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Computer-Assisted Provision of Reproductive Health Care

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Eleanor Bimla Schwarz, University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT00829517
First received: January 23, 2009
Last updated: February 15, 2012
Last verified: February 2012

January 23, 2009
February 15, 2012
January 2011
November 2011   (final data collection date for primary outcome measure)
  • self-reported use of hormonal or more effective contraception [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • receipt of screening for sexually transmitted infection [ Time Frame: 3 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00829517 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Computer-Assisted Provision of Reproductive Health Care
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).

Data collection has been completed

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Health Services Research
  • Contraception
  • Sexually Transmitted Diseases
  • 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
  • Other: STI module
    computer module available at a kiosk that will encourage women to be screened for chlamydia
    Other Name: Chlamydia kiosk
  • Active Comparator: STI kiosk
    computer-assisted provision of screening for chlamydia
    Intervention: Other: STI module
  • Experimental: contraceptive kiosk
    computer-assisted provision of hormonal contraception
    Intervention: Other: computer-assisted provision of hormonal contraception
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
814
November 2011
November 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

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

Exclusion Criteria:

  • women who do not speak English or Spanish
Female
18 Years to 45 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00829517
SFP2-8
Yes
Eleanor Bimla Schwarz, University of Pittsburgh
University of Pittsburgh
Not Provided
Principal Investigator: Eleanor B Schwarz, MD, MS University of Pittsburgh
University of Pittsburgh
February 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP