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NCT00883389 Clinical Trial

Med-alert Bracelet in Chronic Kidney Disease

Chronic Kidney Disease Clinical Trial

Official title:
Safe Kidney Care Med-Alert Bracelet/Keytag

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00883389
Other study ID # HP-00041163
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2008
Est. completion date May 2010

Study information
Verified date October 2019
Source University of Maryland, Baltimore
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a pilot observational study to evaluate subjects with chronic kidney disease acceptance of an alert device linked to an informational website intended to increase recognition of chronic kidney disease, and to guide patients and providers to the safe delivery of care required for this disease. Primary device was a bracelet with the alternative of a key fob with same information supplied when requested. Patients usage of the device was evaluated by survey with Likert scale as to whether the device is 0 = not useful, 1 = somewhat useful, 2 = extremely useful

Description:

No need for more extensive description

Recruitment information / eligibility
Status Completed
Enrollment 26
Est. completion date May 2010
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Persons with chronic kidney disease defined as estimated glomerular filtration rate of < 60 ml/min/1.73m2.

Exclusion Criteria:

- Persons expected to be on dialysis within 6 months.

- Less than 18 years of age

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Medical Alert Bracelet
Medical Alert Bracelet alerting health care providers to consider the patient's chronic kidney disease condition when planning care. It also provides a link to a website about safe kidney care (safekidneycare.org)

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Maryland, Baltimore

Outcome
Type Measure Description Time frame Safety issue
Primary Qualitative Survey Assessmentof Perceived Usefulness of the Med-alert Device. Qualitative questionnaire with primary assessment: "How useful do you think the Med-alert device will be for future healthcare". Response recorded based on a Likert scale with response of 0 = not useful, 1 = somewhat useful, 2 = extremely useful 3 months
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