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Self Management in Urinary Catheter Users

Self-management of Urine Flow in Long-term Urinary Catheter Users

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00883220
Enrollment
202
Registered
2009-04-17
Start date
2009-06-30
Completion date
2012-06-30
Last updated
2012-09-18

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

Conditions

Neurogenic Bladder, Urinary Retention

Keywords

self management, chronic condition, urinary catheter

Brief summary

Learning to self-manage urine flow may help people prevent or minimize persistent complications from long-term indwelling urethral or suprapubic catheters.

Detailed description

Urinary catheter users commonly experience adverse health effects, such as urinary tract infection (UTI), blockage, dislodgement, and leakage, leading to poor quality of life indicators. Catheter-related problems often require health care utilization resulting in increased health care costs. Self-management of urine flow is an essential part of self-care for people with long-term urinary catheters and may lead to prevention or reduction of catheter-related problems and improved quality of life.This study tests the effectiveness of a urinary catheter self-management intervention in a randomized trial of 220 patients, with 12 months of follow-up. The experimental intervention is designed to enhance self-management of urine flow in individuals with long-term urinary catheters, with the goal of decreasing catheter related complications and enhancing quality of life.

Interventions

BEHAVIORALSelf-management of urinary catheter

Awareness, self-monitoring, and self-management of urine flow are taught. Focus is on attaining adequate and consistent levels of fluid intake and preventing catheter dislodgement.

Sponsors

Visiting Nurse Service of New York
CollaboratorOTHER
University of Rochester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Have an indwelling urethral or suprapubic catheter and expect to use it for at least one year. * Live in Central or Western New York State (Utica to Buffalo regions approximately)OR are cared for by the Visiting Nurse Service of New York City. * Able to complete study measurements alone or with the help of a family member or caregiver. * Able to communicate with the study personnel in English. * Have access to a telephone for data collection.

Exclusion criteria

* Terminally ill * Cognitively impaired * No catheter associated UTI within the previous 12 months NOR blockage NOR dislodgement in the previous 6 months(only in people who have had the catheter for 12 months or more)

Design outcomes

Primary

MeasureTime frame
Symptomatic urinary tract infectionevery two months for 12 months

Secondary

MeasureTime frame
Urinary catheter quality of life6 months and 12 months

Countries

United States

Outcome results

None listed

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