Protein-Energy Malnutrition, Renal Failure
Conditions
Keywords
peritoneal dialysis
Brief summary
This is a 6-month prospective interventional clinical trial designed to evaluate the impact of whey protein isolate oral supplement on protein status. Differences in protein status will be evaluated with review of the medical chart from standard of care monthly blood collection for serum albumin, total protein, and normalized protein catabolic rate (nPCR) as detected by serum urea nitrogen. Mid-arm circumference and weight will be measured to ensure no significant changes. Quality of life will be measured to detect if the addition of protein aided in overall quality of life. There will be a 3-month recruitment period prior to the start of the trial to ensure the potential participants are familiarized with the clinical trial. After the recruitment period has finished, eligible participants will sign the consent form in order to participate in the study. At this point, participants will be provided the supplements for the month and instructed with the amount of water and how to mix with the provided measuring and drinking cup.
Interventions
DIETARY_SUPPLEMENTWhey protein supplement
A monthly supply of 35 g of whey protein isolate will be provided to participants in individual sachet packets with instructions of preparation. Every month, participants will come to the center to provide the standard monthly blood sample. At this time, the PI will have participants complete the quality-of-life instrument, ask if there have been any changes in their dietary habits, and collect weights for up to 6-months. Additionally, participants will indicate if they had consumed the protein daily and/or bring back their empty/full satchel packets. As this is a feasibility trial, it is necessary to determine the compliancy of consuming protein daily and the amount. Furthermore, understanding how protein markers may be affected by consumption of the protein daily vs less frequently throughout the week is important to establish improved recommendations for consumption of protein supplements.
Sponsors
University of Florida
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Intervention model description
6-month prospective interventional clinical trial
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 18 years old or older * diagnosed with stage 5 Chronic Kidney Disease for at least 3 months prior to the starting date of the trial * on peritoneal dialysis at least three months prior to the starting date of the trial * can provide signed informed consent * have no dietary restriction * no food allergies * no chewing/swallowing difficulties.
Exclusion criteria
* not meeting the above * pregnant/lactating as either self-reported or determined by the medical director * Chronic Kidney Disease patient stages 1-4. * Chronic Kidney Disease patient undergoing hemodialysis. * use of other protein supplement
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Serum albumin | up to 6 months of the study | Collection of serum albumin to identify a change from pre-post to analyze the effect protein isolate had on inflammation marker and protein status. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Total protein | up to 6 months of the study | Collection of whole blood total protein to identify a change from pre-post to analyze the effect protein isolates had on protein stores. |
| normalized protein catabolic rate (nPCR) | up to 6 months of the study | Collection of nPCR through serum to identify a change from pre-post to analyze the effect protein isolates had on nPCR. |
| mid-arm muscle circumference | up to 6 months of the study | measuring mid-arm circumference from baseline to the end of the study to determine that protein isolates did not affect muscle mass. |
Countries
United States
Outcome results
None listed