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Internet Self-Management for People With Intermittent Urinary Catheters

Web-Based Self-Management Intervention for Intermittent Urinary Catheter Use

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02168465
Acronym
Internet CIC
Enrollment
34
Registered
2014-06-20
Start date
2013-06-30
Completion date
2015-02-28
Last updated
2015-05-07

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

Conditions

Spinal Cord Injury

Keywords

self-efficacy, self-management, web-based intervention research

Brief summary

1. Design and develop web-based self-management intervention to improve catheter-related outcomes and quality of life in people with spinal cord injury (SCI). 2. Conduct a pilot study to assess the feasibility (i.e., acceptability and usability of the website application) and preliminary effectiveness of this new self-management intervention. 3. Develop and test the reliability of new/modified measures (intermittent catheter self-efficacy and self-management).

Detailed description

Stages involve: (1) Develop an Internet-based intervention to improve self-management and outcomes related to clean intermittent catheterization (CIC) among people with SCI (2) Pretest the Internet application with five persons with SCI using CIC; and (3) Conduct a web-based six-month intervention pilot study in a group of 30 with SCI using CIC. Outcomes are: catheter-related adverse health outcomes (e.g., UTI, urine leakage), CIC self- management, CIC self-efficacy, health related expenditures and quality of life. Information from this study will be used to modify the Internet application for a future Phase 2 trial in a larger study.

Interventions

BEHAVIORALteaching self-management of an intermittent catheter

Specifically, we will teach awareness, self-monitoring and self-management strategies to CIC uses with SCI in an online format. Nurse telephone consultation for teaching self-management will be combined with peer leaders for online forums.

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
University of Rochester
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

Individuals will be included if they are English speaking adults over 18 years with an SCI and are interested in participating. Inclusion criteria are: 1. use of CIC for regular bladder drainage, 2. expect to use CIC indefinitely or for at least nine months, and 3. access to and ability to use a computer and telephone. Computer and telephone use may be voice activated for those with little hand use. Study participants do not need to perform CIC entirely themselves, as people with limited hand dexterity may have caregivers who do the procedure. They do need to be able to use the computer and telephone however. Additional inclusion criteria for the five persons in the intervention and pretesting group (described below in III, 1) include: 1. having used CIC for regular bladder drainage for at least one year and 2. expect to use CIC indefinitely or for at least one more year. People will need to have used CIC for at least a year so that they are well experienced in CIC because the two Peer Leaders will be selected from this group.

Exclusion criteria

* People will be excluded if they cannot communicate in English, * Are terminally ill, or are expected to discontinue CIC within the next nine months. - Non-English speaking people will not be included because translated instruments (e.g., Spanish) are not available for all measures and doing this as a part of this small study might compromise the integrity of this first test of preliminary effectiveness.

Design outcomes

Primary

MeasureTime frameDescription
catheter-related adverse health outcomes (e.g., UTI, urine leakage)pre-post 3 month intervention in a single groupcatheter related adverse events will be reported by internet based survey about 3 months after enrollment

Secondary

MeasureTime frameDescription
Intermittent catheter self-efficacy,pre-post 3 month intervention in a single groupIntermittent catheter confidence related to self-care capability

Other

MeasureTime frameDescription
Intermittent catheter self-managementpre-post 3 month intervention in a single groupSelf-care management involves specific activities performed by the person to manage their intermittent catheter.

Countries

United States

Outcome results

None listed

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