Codesign of an Optical Device to Measure Urine Flow and Volume

Teesside University

Status

Not yet enrolling

Conditions

Urinary Retention

Urinary Tract Infections

Benign Prostatic Hyperplasia

Underactive Bladder

Urinary Incontinence

Overactive Bladder

Treatments

Other: Focus Group

Study type

Observational

Funder types

Other

Identifiers

NCT05576311

10852

Details and patient eligibility

About

The study is seeking to understand the needs of patients and healthcare practitioners for an innovation in the way that changes in bladder function are assessed. This information will be used in the design and evaluation of a device, being developed in parallel, that assesses changes to the volume and flow of urine in order to determine changes in bladder function.

In order to ensure development is optimal, the principal research objective is therefore to understand the needs of patients and healthcare practitioners (ranging from care home staff and GPs in primary care, to urologists in tertiary referral centres).

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria The participant is willing and able to give informed consent for participation in the study.

Aged 18 years or above. Male or Female.

Exclusion criteria The participant is unwilling or unable to give informed consent for participation in the study.