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
• Status: Not yet recruiting
• Phase: N/A
• 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
• 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

Related Conditions & MeSH terms

• Urethral Stricture

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