Usability Study of the Focus Touch™ Conception System: Semen Collection

Completed · Early Phase 1

Conditions studied: Infertility

In brief

This is a human factors usability study designed to validated usability by obtaining feedback in a home use environment regarding ease of use of the Focus Touch™ Conception System Conceptacle (when used to collect semen) and the instructions for use. The investigators will collect data to demonstrate that the usability requirements of the conception system as collection device, as determined by Usability Specification: Focus Touch Conception System, ER-000001 have been met. The ability of the device to be used during sexual intercourse without discomfort or injury to the female participant's vaginal/cervical tissues shall also be taken into account. Participating couples will be asked to use the Focus Touch™ Conception System Conceptacle (in condom form), using the Instructions For Use, to collect semen during sexual intercourse in a home use environment. This study will involve sexual intercourse between monogamous, heterosexual couples who are trying to conceive or are on a non-vaginal birth control with which they do not normally use condoms. Participants will be asked to complete the study and the questionnaire within 3 days of receiving the study packet. Contact information shall be collected, but participants will only be contacted if they fail to return the questionnaire within the requested timeframe.

Key facts

Study ID

NCT01585012

Run by

Rinovum Women's Health, Inc.

People needed

30

Starts

2012-01-01

Expected to finish

2012-03-01

Last updated by the study team

2015-05-06

Who can join

Age: 20 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Heterosexual, monogamous couples, of any race or ethnicity, who are sexually active
• 20 - 50 years of age
• Signed Informed Consent
• Past experience with using condoms
• Trying to conceive or using a non-vaginal birth control with which they do not normally use a condom.

You may not qualify if…

• Vaginal tract medical interventions with the last three (3) month
• Vaginal prolapse
• Full Hysterectomy

Where it is running

• Forbes Regional Hospital — Monroeville, Pennsylvania, United States

Full record on ClinicalTrials.gov

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