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Women's Input on Sexual Health

NCT02057419 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8

Last updated 2025-10-24

Study results available
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Summary

The purpose of this study is to answer the following question: How do user sensory perceptions and experiences (USPEs) for IVRS differ between initial and continued use and how can this knowledge help product developers better understand how to design new IVR products and develop behavioral (or point-of-care) interventions to optimize use?

Conditions

  • Intravaginal Ring Use

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • The Miriam Hospital

    lead OTHER

Principal Investigators

  • Kate Guthrie, PhD · The Miriam Hospital: Centers for Behavioral & Preventive Medicine

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-04-14
Primary Completion
2016-06-24
Completion
2018-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02057419 on ClinicalTrials.gov