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NCT01184157 Clinical Trial

Randomized Trial of Home Versus Clinic-based Screening for Sexually Transmitted Infections

Gonorrhea Clinical Trial

Official title:
Randomized Trial of Home Versus Clinic-based Screening for Sexually Transmitted Infections in Long-Acting Reversible Contraceptive Users

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01184157
Other study ID # 07-0256
Secondary ID
Status Completed
Phase N/A
First received August 17, 2010
Last updated August 17, 2010

Study information
Verified date August 2010
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study randomizes women using long-acting reversible methods of contraception to home-based STD screening through the mail compared to screening available in a clinical setting. We hypothesize that women randomized to home-based screening will be more likely to complete screening.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group 14 Years to 45 Years
Eligibility Inclusion Criteria:

- Participant in Contraceptive CHOICE cohort study

- Using a long-acting reversible method of contraception

- Completed baseline clinical survey in the Contraceptive CHOICE cohort study

Exclusion Criteria:

- Living outside the United States at time of annual STI screening

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening

Related Conditions & MeSH terms

Intervention

Behavioral:
• Home screening

• Clinic screening

Locations
Country Name City State
United States Washington University School of Medicine St. Louis Missouri

Sponsors (1)
Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of tests received No
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