A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas

Recruiting N/A Interventional Study
Incontinence Prolapse
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Other
Participants needed
357 (estimated)
Sponsor
University of Alabama at Birmingham · Other
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About This Trial
There are 3 aims of this study. In Aim 1 community patient partners will be enrolled to help guide the research being performed in all of the aims. Investigators will also administer a survey that will help determine factors associated with surgical preparedness. In Aim 2 investigators will develop an intervention to increase surgical preparedness using Human Centered Design Methods. Aim 3 will pi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Patients who * Self-report as female * 18 years and older * Self-report as Hispanic ethnicity * Scheduled to undergo a surgery for a urogynecologic condition in the operating room (surgery to correct pelvic organ prolapse, urinary/fecal incontinence, fistula, urethral masses) *…
Contacts

Gabriela Halder, MD, MPH

205-934-5498

gehalder@uabmc.edu

CONTACT