View Clinical Trial (Medical Research Study)
Dietary Adherence Enhancement in Peritoneal Dialysis: BalanceWise-PD - NCT00447317-15213(Clinical Trial 165571)
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Pittsburgh |
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State:
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PA |
| Zip Code: |
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15213 |
| Conditions: |
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End-Stage Renal Disease |
| Purpose: |
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This randomized study will pilot test an intervention, based on self-efficacy theory and
involving personal digital assistant (PDA)-based dietary self-monitoring, to improve
adherence to the peritoneal dialysis dietary regimen. 60 individuals, 21 years of age or
older, who are on continuous ambulatory peritoneal dialysis or nightly cycler peritoneal
dialysis, will be recruited to the study. Participants will be randomized to one of 2
groups. Group A will receive a 4-month active intervention of decreasing intensity over
time delivered via mail, telephone, and during regularly scheduled dialysis clinic visits.
Group B will receive a 4-month attention control experience in which they receive
reinforcement of standard dietary education. With this study the investigators will:
1. Explore the impact of the intervention on dietary sodium intake,
2. Explore the intervention on blood pressure,
3. Explore the impact of the intervention on morning post dialysis weight (i.e. weight
after conclusion of continuous cycling peritoneal dialysis (CCPD) or after long dwell
for continuous ambulatory peritoneal dialysis (CAPD) patients, AND
4. Explore the feasibility and acceptability of the intervention
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
The investigators will recruit those individuals:
- who are 18 years of age or older,
- who are literate, community-dwelling adults, and
- who have been receiving maintenance PD for at least 3 months. Individuals on
maintenance PD less than 3 months are excluded to allow for patients to adjust to the
PD regimen, and for stabilization of nutritional status in the early weeks of
dialysis (i.e. they may be considered for the study after 3 months of dialysis)
Exclusion Criteria:
Excluded from the study will be individuals:
- who are deemed by dialysis center staff to have a problem with cognitive function
and to be chronically noncompliant to the dialysis regimen (e.g. misses multiple
appointments and dialysis treatments),
- those who cannot read or write, those who do not speak English,
- those who plan to move out of the area or change dialysis centers within the next 5
months,
- those with a terminal illness and life expectancy of less than 12 months,
- those who are scheduled for a living donor transplant,
- individuals who cannot see the PDA screen or use the stylus to make selections from
the PDA screen, or
- individuals who are living in a nursing home or personal care facility, who would
have limited control over their dietary intake |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 11, 2010 |
Modifications to
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above to view all information about this clinical trial. |
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