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NCT06384066 Clinical Trial

Mobile Health Application to Improve Patient Satisfaction After Urethroplasty

Urethral Stricture Clinical Trial

Official title:
Evaluation of a Mobile Health Application to Improve Patient Satisfaction and Outcomes After Urethroplasty: a Prospective Randomized Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06384066
Other study ID # STU00219774
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 2024
Est. completion date December 2024

Study information
Verified date April 2024
Source Northwestern University
Contact Emily Ji
Phone 312-695-8146
Email emily.ji@nm.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Create a custom urethroplasty mobile application that will guide patients through through the surgical process.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 80
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 89 Years
Eligibility Inclusion Criteria: - 18 years of age or older - Have a Urethral stricture and are under going urethroplasty surgery Exclusion Criteria: - Patients that do not have mobile phone capabilities - Patients who have physical or cognitive impairment when using a mobile phone or answering questionnaires - Inability to provide consent to the study

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• GetWell Mobile Application
GetWell utilizes an interactive health care application to allow patients to participate in their care. We plan to work with GetWell to develop a custom built plan for urethroplasty patients and provide patient education.
• Standard of Care
Office Based Pathway

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Northwestern University

Outcome
Type Measure Description Time frame Safety issue
Primary Improve patient satisfaction, education and reported outcomes Asses through Patient reported outcome measurement survey, Urethral Stricture Symptom and Impact Measurement and Patient-Reported Outcomes Measurement information System 29-item profile (PROMIS) which assesses pain intensity using a 0-10 rating item, with higher scores being a worse outcome. 0 to 3 months
Primary Change in rate of patient phone calls and messages assess through chart review to evaluate the number of chart messages and phone calls 0 to 12 months
Primary Rate of emergency department visits Assess through chart review and patient reporting events. 0 to 12 months
See also
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