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A virtual coach for surgery: can it empower latina patients?

NCT ID NCT06679621

Symptom relief Sponsor: University of Alabama at Birmingham Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 14, 2026 · Last updated Aug 14, 2026

Summary

This study tests a telehealth program designed to help Latina patients feel more prepared for urogynecologic surgery, such as procedures for incontinence or pelvic organ prolapse. The program is being developed with input from patient partners and uses human-centered design. Researchers will first survey patients to understand what affects surgical preparedness, then build the intervention, and finally pilot-test it to see if it is feasible, acceptable, and useful. The goal is to support patients in feeling more informed and confident before their operation.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A telehealth intervention designed with input from patients to increase surgical preparedness
What this could lead to
If successful, this could provide a practical way to help Latina patients feel more prepared and confident before urogynecologic surgery, potentially improving their experience and outcomes.
What could go wrong
This is an early pilot focused on feasibility, not on proving the intervention improves health outcomes. Results may not apply to all patients or settings.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 357 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2024

Expected to finish

Jun 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

pelvic organ prolapse Prolapse

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Incontinence Prolapse

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University of Alabama Birmginham

    RECRUITING

    Birmingham, Alabama, 35294, United States

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