Telehealth program to help Latinas prepare for urogynecologic surgery
Official title: A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas
Run by University of Alabama at Birmingham · NCT06679621 · Data updated 2026-11-12
This study is testing a telehealth program to help Latina women get ready for urogynecologic surgery and see if it makes the process easier for them.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 357 (estimated) |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Birmingham, Alabama) |
| Status | Recruiting |
| Started | November 1, 2024 |
| Main results expected | June 1, 2027 |
| Study ends | June 1, 2027 |
| Registry record updated | August 14, 2026 |
| Trial ID | NCT06679621 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are Hispanic females aged 18 and older who are scheduled for urogynecologic surgery.
✕Probably not a fit
Patients who are male, under 18, or not of Hispanic ethnicity will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This project aims to enhance surgical preparedness among Latinas undergoing urogynecologic surgery through a telehealth intervention called TIPPS-Latina. The study involves three main aims: engaging community patient partners to guide research, developing the intervention using Human Centered Design methods, and pilot testing the intervention to assess its feasibility and implementation outcomes. The research will utilize a participatory action framework and mixed methods to gather insights and refine the intervention based on patient preferences. Surgical preparedness will be evaluated using a validated survey specifically designed for this population.
Why it matters
Potential benefit: If successful, this intervention could significantly improve surgical preparedness and outcomes for Latina patients undergoing urogynecologic surgery.
How similar studies have gone: While similar telehealth interventions have shown promise in other populations, this specific approach tailored for Latinas is novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion 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) * 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 Criteria: 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
Where it's running
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University of Alabama Birmginham
Birmingham, Alabama, United States Recruiting
Study contacts
- Principal investigator: Gabriela Halder, MD, MPH — Assistant Professor
- Study coordinator: Gabriela Halder, MD, MPH
- Email: gehalder@uabmc.edu
- Phone: 205-934-5498
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.