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.
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