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UnknownNCT05205733

Expanding Fertility Care to Poor and Low Resourced Settings Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
University of California, San Francisco · Academic / Other
Sex
Male
Age
18 Years – 64 Years
Healthy volunteers
Accepted

Summary

The investigators currently lack an understanding of barriers to completing the male factor infertility evaluation. Furthermore, as the investigators continue to expand access to fertility treatment particularly within low-resourced settings, it is important that all aspects of infertility within a couple are equally explored. The COVID-19 pandemic has disproportionately affected low-income communities and communities of color at greater rates in terms of not only disease morbidity/mortality but how medical systems are accessed and care is delivered.

Detailed description

This pilot study was designed to help providers identify barriers to completing the basic infertility work-up in a low resource setting with a focus on accessibility and feasibility of semen analysis testing. As a pilot study, a total of 60 male partners of patients who are seeking infertility treatment at the Zuckerberg San Francisco General Hospital Gynecology clinic will be recruited. Participants will be randomized to completing a semen analysis by either the standard in-clinic test or an at-home sperm testing kit. The investigators hypothesis is that there will be an increase in participants completing their semen analysis when using the at-home sperm testing kit as opposed to having to come to the lab. Specific Aims: 1. To identify barriers to completing a semen analysis. 2. To compare barriers unique to completing an in-clinic versus at-home testing. 3. To compare satisfaction scores with in-clinic versus at-home testing. 4. To compare the time to complete the semen analysis with in-clinic versus at-home testing. 5. To compare the time to initiating treatment after completing in-clinic versus at-home testing. Patients seen at Zuckerberg San Francisco General who are currently undergoing an infertility evaluation as a part of the basic infertility assessment will be contacted. Consented participants will be randomized to complete an at home vs. lab semen analysis. After the semen analysis is completed, participants will be sent a comprehensive questionnaire regarding their experience, level of satisfaction, and barriers with completion of the recent semen analysis. Participants will be given 3 months to complete the semen analysis. If not completed in this timeframe, participants will be sent a different comprehensive questionnaire regarding their barriers with completion of the semen analysis. Additional clinical questions include time from semen analysis order to completion as well as time from semen analysis completion to start of treatment plan.

Conditions

Interventions

TypeNameDescription
OTHERMail-in semen analysis kitPresumably an easier, convenient, and more comfortable way to provide a semen analysis with an in-home mail-in semen analysis kit

Timeline

Start date
2022-05-24
Primary completion
2024-06-01
Completion
2024-06-01
First posted
2022-01-25
Last updated
2024-02-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05205733. Inclusion in this directory is not an endorsement.