Healthy Clinical Trial
Official title:
Assessing Novel Methods of Improving Patient Education of Nutrition: eHealth, Health Literacy and Chronic Kidney Disease
1. Research question Can a web-based nutritional educational intervention improve
phosphorus knowledge and control of phosphorus intake?
2. Experimental design
Following enrollment and informed consent, subjects will be randomized to one of two
arms (group1: usual care; group 2: usual care plus Internet-based nutrition module).
All subjects will undergo baseline data collection, consisting of:
1. Short form of the test of functional health literacy in adults: categorizes
individuals as having adequate, marginal or inadequate health literacy.
2. Chronic Kidney Disease (CKD) Knowledge Assessment Tool: addresses nutritional
knowledge of CKD.
3. SF-12 Health Survey version 2: a 12-item measure of health related quality of
life.
4. Kidney Disease Self-Management Survey: a 58-item Likert scale based on theories
important for self-management in chronic disease.
5. 3-Day Dietary Diaries
6. Lab work:
i. Serum phosphorus, calcium and parathyroid hormone levels. ii. Circulating
endothelial cells, a novel marker for vascular damage.
Following baseline data collection, group 1 will continue with their scheduled clinic
visit, while group 2 will spend approximately 30 minutes completing a web-based
nutrition module. After completion of the module, patients will proceed with their
scheduled clinic visit.
All subjects will then be asked to return in 30-60 days to repeat some of the survey
information and blood work
3. Major risks to subjects There is the potential for some mild discomfort from the
necessary blood draws, which occur twice per subjects.
4. Potential benefits to subjects Subjects randomized to the web-based module may receive
an educational benefit from it.
5. Consent procedures Only individuals who can provide their own consent can participate.
Upon agreeing to enroll, a study coordinator or investigator will provide the subject
with a copy of the consent form, and will remain available to answer any questions.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 2008 |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - none - study withdrawn Exclusion Criteria: - none - study withdrawn |
N/A
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Wisconsin, Madison |
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