A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas
University of Alabama at Birmingham
357 participants
Nov 11, 2024
INTERVENTIONAL
Conditions
Summary
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 pilot test the intervention using mixed methods to determine feasibility and implementation outcomes.
Eligibility
Inclusion Criteria10
- Patients who
- Self-report as female
- 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)
- Able to read and write English and/or Spanish
- Urogynecologists who -Routinely perform urogynecologist surgeries to correct pelvic organ prolapse, urinary/fecal incontinence, fistula, urethral masses
- Nurses who
- Spend most of their time at a urogynecologic clinic
- Engage in the process of preparing patients for urogynecologic surgery
Exclusion Criteria11
- Patients who
- Self-report as male
- Are less than 18 years of age
- Self-report as not of Hispanic ethnicity
- Scheduled to undergo a surgery for a condition that is not urogynecologic or is not in the operating room
- Patients undergoing procedures that are traditionally performed in the office (bladder Botox, pelvic floor Botox, urethral bulking)
- Urogynecologists who
- Do not routinely perform urogynecologic surgery
- Nurses who
- Do not spend most of their time at a urogynecology clinic
- Do not engage in the process of preparing patients for urogynecologic surgery
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
This telehealth intervention will be made using human centered design methods
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06679621