A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Alabama at Birmingham
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 pilot test the intervention using mixed methods to determine feasibility and implementation outcomes.
Eligibility criteria
Qualifiers
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)
Disqualifiers
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
Trial design
Treatments tested in this trial
- Telehealth intervention
Treatment groups
357 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of Alabama at Birmingham
Lead sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator
Source ClinicalTrials.gov