Mobile Health Application to Improve Patient Satisfaction After Urethroplasty

NCT ID: NCT06384066

Last Updated: 2024-11-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-28

Study Completion Date

2024-09-11

Brief Summary

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

Detailed Description

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Conditions

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Urethral Stricture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Standard of Care

Standard Care

Group Type OTHER

Standard of Care

Intervention Type OTHER

Office Based Pathway

Standard Care + GetWell App

Group Type OTHER

GetWell Mobile Application

Intervention Type OTHER

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

Intervention Type OTHER

Office Based Pathway

Interventions

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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.

Intervention Type OTHER

Standard of Care

Office Based Pathway

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

89 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Northwestern University

OTHER

Sponsor Role lead

Responsible Party

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Ziho Lee

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Northwestern University

Chicago, Illinois, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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STU00219774

Identifier Type: -

Identifier Source: org_study_id

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