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Benign Prostatic Hyperplasia (BPH) Mobile Application Pilot Study

The Feasibility and Acceptability of a (Mobile) Application for Men With LUTS/BPH: a Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03228485
Enrollment
200
Registered
2017-07-25
Start date
2019-04-04
Completion date
2023-03-01
Last updated
2025-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower Urinary Tract Symptoms, Prostatic Hyperplasia

Keywords

Smartphone, Application, Pilot, mhealth

Brief summary

This study assesses the feasibility, and acceptability of a (mobile) application for men presenting at their physician's office with LUTS/BPH; starting with medical therapy and naïve for treatment. Patients will be enrolled in the study by their physician (GP or urologist). The patients will receive a daily medication reminder including frequent feedback on medication adherence. Furthermore, standard questionnaires will be filled out via the application. The hypothesis of this pilot study is that application is feasible and accepted in this group of patients.

Detailed description

Rationale: One of the next developments in healthcare is digitalization, including (mobile) applications that could support healthcare providers. A significant number of aging men suffer from lower urinary tract symptoms (LUTS), often caused by benign prostate hyperplasia (BPH). LUTS/BPH is primarily treated by physicians (GPs or Urologists). Optimal evaluation of patients with LUTS/BPH, treatment selection and follow-up by the physicians and medication adherence are essential in the management of LUTS. This pilot project represents a strong collaboration between a urological association, urologists, and physicians in supporting healthcare improvement for LUTS/BPH with the use of a (mobile) application. The hypothesis is that the (mobile) application can support the patient in medication adherence and improve the adherence by feedback and that the application can help to collect objective disease information with electronic questionnaires. Objectives: The primary objective is to assess the feasibility, and acceptability of a (mobile) application for men presenting at their general practitioner/or urologist with LUTS/BPH who are either: under treatment, or who may require medical therapy for the first time. The secondary objectives are to identify potential gaps, clarify controversial points of the application, to document the communication between patients, physicians and supervising urologists in order to optimize (if necessary) the application, to assess medication adherence and to record if treatment provided by physicians is in compliance with the guidelines recommendations.

Interventions

DEVICEMyBPH Care mobile app

The application that will give daily medication reminders and via which the questionnaires can be filled out.

Sponsors

Société Internationale d'Urologie
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male * Age ≥ 40 * Bothersome LUTS * Start of medical therapy for LUTS * Either: 1. No previous LUTS/BPH treatment (medical or invasive), or 2. Under medical treatment * In possession of a smartphone, tablet or computer with internet connection * Access to email * Fluent speaking and reading of the national language * Signed informed consent

Exclusion criteria

* Previous LUTS/BPH treatment with surgery * Previous pelvic surgery or radiotherapy * History of neurological disease * History of bladder or prostate cancer * Unable to provide informed consent * Analphabet * Unable to operate a smartphone/ tablet/computer * Incapable of understanding the language in which the information for the patient is given

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of a mobile application for LUTS6 monthsThe feasibility is assessed by the application use for men presenting at their general practitioner/or urologist with LUTS/BPH who are either: under treatment, or who may require medical therapy for the first time. The patient application will be judged as Definitely Feasible if the study is completed for ≥70% eligible patients, Possibly Feasible (completed for 50-69% eligible patients) or Not Feasible (completed for \<50%).

Secondary

MeasureTime frameDescription
Acceptability and satisfaction of a mobile application for LUTS6 monthsIn order to assess the acceptance and satisfaction of the mobile application including the application subjective quality and perceived impact, a questionnaire will be used. This questionnaire is based on a standardized application rating questionnaire, namely the user Mobile Application Rating Scale (uMARS). Outcomes are described and compared between centers.
Medication adherence6 monthsSelf-reported medication adherence by the patient via the application over the full period of the pilot.
Compliance to guidelinesAt baselineDescriptive comparison between the medication prescribed by the physician and the advised medication according to the international guidelines based on the patient characteristics.
Referral networkAt the end of the 6 months periodEvaluation of the referral communication between the physicians and the supervising urologist by questions in the final questionnaire.

Countries

Greece, Italy, Portugal, Spain, Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026