RECRUITING

A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas

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Conditions

IncontinenceProlapse

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas

Quick Facts

Study Start:2024-11-11
Study Completion:2027-11-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06679621

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-report as female
  2. * 18 years and older
  3. * Self-report as Hispanic ethnicity
  4. * 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)
  5. * Able to read and write English and/or Spanish
  6. * Spend most of their time at a urogynecologic clinic
  7. * Engage in the process of preparing patients for urogynecologic surgery
  1. * Self-report as male
  2. * Are less than 18 years of age
  3. * Self-report as not of Hispanic ethnicity
  4. * Scheduled to undergo a surgery for a condition that is not urogynecologic or is not in the operating room
  5. * Patients undergoing procedures that are traditionally performed in the office (bladder Botox, pelvic floor Botox, urethral bulking)
  6. * Do not spend most of their time at a urogynecology clinic
  7. * Do not engage in the process of preparing patients for urogynecologic surgery

Contacts and Locations

Study Contact

Gabriela Halder, MD, MPH
CONTACT
205-934-5498
gehalder@uabmc.edu

Principal Investigator

Gabriela Halder, MD, MPH
PRINCIPAL_INVESTIGATOR
Assistant Professor

Study Locations (Sites)

University of Alabama Birmginham
Birmingham, Alabama, 35294
United States

Collaborators and Investigators

Sponsor: University of Alabama at Birmingham

  • Gabriela Halder, MD, MPH, PRINCIPAL_INVESTIGATOR, Assistant Professor

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-11
Study Completion Date2027-11-01

Study Record Updates

Study Start Date2024-11-11
Study Completion Date2027-11-01

Terms related to this study

Additional Relevant MeSH Terms

  • Incontinence
  • Prolapse