A Nutritional Intervention for Diabetic Neuropathy (WCCR-DN2)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01953757|
Recruitment Status : Completed
First Posted : October 1, 2013
Last Update Posted : April 27, 2015
|First Submitted Date ICMJE||September 26, 2013|
|First Posted Date ICMJE||October 1, 2013|
|Last Update Posted Date||April 27, 2015|
|Study Start Date ICMJE||September 2013|
|Actual Primary Completion Date||March 2015 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
||Pain [ Time Frame: 20 weeks ]
Pain will be measured follow the baseline and 20 week score using the following assessment tools: Michigan Neuropathy Screening Instrument Norfolk Quality of Life Questionnaire Neuropathy Impairment Score - Lower Limbs Neuropathy Total Symptom Score 6 Neuropathy Pain Scale McGill Pain Questionnaire Global Impression Scale
|Original Primary Outcome Measures ICMJE||Same as current|
|Current Secondary Outcome Measures ICMJE
|Original Secondary Outcome Measures ICMJE||Same as current|
|Current Other Pre-specified Outcome Measures
||Acceptability of vegan diet [ Time Frame: 20 Weeks ]
Acceptability of vegan diet will be measured by change in score at baseline and 20 weeks using the Eating Inventory questionnaire.
|Original Other Pre-specified Outcome Measures||Same as current|
|Brief Title ICMJE||A Nutritional Intervention for Diabetic Neuropathy (WCCR-DN2)|
|Official Title ICMJE||A Nutritional Intervention for Diabetic Neuropathy (WCCR-DN2)|
The purpose of this study is to assess whether, in individuals with diabetic neuropathy, a low-fat, vegan diet in combination with a vitamin B12 supplement improves pain, sensation and other subjective symptoms, more effectively than a vitamin B12 supplement with no diet changes. The principal measure is pain as measured by the following assessment tools: Michigan Neuropathy Screening Instrument, Norfolk Quality of Life Questionnaire, Neuropathy Impairment Score - Lower Limbs, Neuropathy Total Symptom Score, Neuropathy Pain Scale, McGill Pain Questionnaire and Global Impression Scale. The study duration is 20 weeks.
This study also examines the effects of a low-fat, vegan diet on mood, using the Center for Epidemiologic Studies Depression Scale-Revised, and the Beck Depression Inventory.
The following determinations will be made at baseline, mid-point, and end of each 20-week study period, as well as at one-year follow up:
General status, symptoms, and medication accounting. Participants will be asked to report changes in their health and medication use.
Disease Activity. The following assessments will be used to measure pain and changes in sensory perception related to diabetic neuropathy:
Michigan Neuropathy Screening Instrument. The MNSI questionnaire consists of 15 questions followed by a single 8-point clinical examination involving inspection of the foot, assessment of ankle reflexes, and semi-quantitative determination of vibration perception.
Norfolk Quality of Life Questionnaire Norfolk QOL-DN is a 47-item questionnaire developed by the Eastern Virginia Medical School, Norfolk, VA, for assessing subjects' perception of the effects of diabetes and diabetic neuropathy. It consists of 28 items pertaining specifically to to small fiber, large fiber and autonomic nerve function symptoms, and activities of daily living (ADL).
Neuropathy Impairment Score for Lower Limbs (NIS-LL) The NIS-LL is the lower limb component of the full Neuropathy Impairment Score (NIS) and has 3 domains including: muscle weakness, reflexes, and sensation. The maximum score is 88 points. Based on experience with and data collected from these clinical trials, the Peripheral Nerve Society considers a 2 point change on the NIS-LL to correspond to a meaningful change in clinical status.
Neuropathy Total Symptoms Score (NTSS-6) Neuropathy total symptom score-6 (NTSS-6) is a neuropathy sensory symptom scale that is designed to evaluate the frequency and intensity of individual neuropathy sensory symptoms identified frequently by patients with DPN. A total of six questions are synthesized to identify and quantify the specific positive and negative symptoms associated with sensory deficits in patients.
Neuropathy Pain Scale In order to assess and differentiate qualities of pain, Galer and Jensen developed the Neuropathic Pain Scale (NPS) in 1997. The NPS is composed of 10 items that assess two global pain domains including pain intensity and unpleasantness, and six pain qualities, including sharp, hot, dull, cold, sensitive, and itchy pain, in two dimensions (internal and cutaneous).
McGill Pain Questionnaire The McGill Pain Questionnaire (MPQ) is used to specify subjective pain experience using sensory, affective and evaluative word descriptors. The short form of the McGill Pain Questionnaire (SF-MPQ) contains 11 questions referring to the sensory dimension of the pain experience and four related to the affective dimension.
Global Impression Scale Global impression scale (GIS) is also termed global rating of change scales (GRC) and was developed to assess patients' overall improvement or deterioration in a clinical setting, and has been frequently used in musculoskeletal and chronic pain trials.
Height. Height will be measured at baseline (only) with participants standing barefoot with their backs to a wall-mounted stadiometer and heels against the wall, recorded to the nearest 0.5 cm.
Body weight. With participants wearing light, indoor clothing but without shoes, body weight will be measured to the nearest 0.1 kg, using a digital scale.
Blood pressure. A digital blood pressure monitor and a cuff of a size appropriate to the participant's arm will be used. The cuff size for each participant will be recorded for consistency of use at each visit. Participants will be asked to remove all clothing that covers the location of cuff placement and then rest in a seated position for 5 minutes with legs uncrossed, without talking or reading. The back and arm will be supported such that the middle of the cuff on the upper arm is at the level of the right atrium (the mid-point of the sternum). Three measurements will be taken at 1-minute intervals. The first measurement will be disregarded, and the mean of the remaining 2 measurements will be calculated.
Serum cholesterol and triacylglycerol concentrations will be measured using the Olympus Cholesterol Reagent on Olympus Chemistry Analyzers. HDL-cholesterol will be measured directly using the HDL-C plus 3rd generation test with the Roche direct HDL-cholesterol assay.Low density lipoprotein cholesterol (LDL-C) concentration will be estimated using the Friedewald equation. Plasma triglyceride levels will be measured using Olympus Chemistry analyzers from Quest Diagnostics.
Comprehensive Metabolic Panel. These values will be evaluated at baseline, 20 weeks, and one-year follow-up.
Hemoglobin A1c. Hemoglobin A1c will be measured in whole blood using the COBAS INTEGRA on Roche clinical chemistry analyzers.
Glucose. Plasma glucose will be measured using an Olympus Chemistry Analyzer from Quest Diagnostics, Baltimore, MD, USA.
Urinary albumin and creatinine will be assessed on spot urine samples. Samples for the albumin assay will be tested using the K-Assay High-Sensitive Microalbumin assay from Quest Diagnostics.
Apolipoprotein E (APOE): Participants who consent to this aspect of the study will be genotyped for the ε2, ε3, and ε4 alleles. A sample of approximately 5 ml of the participant's blood is required and will be drawn simultaneously with the 20-week health assessment labs. Individuals with diabetes are at greatly increased risk of developing Alzheimer's disease, and some studies have suggested that the effect of saturated fat intake on Alzheimer's risk may be most evident in (or even limited to) carriers of the APOEε4 allele. The ApoE protein produced by the APOE gene is a major plasma apolipoprotein and the primary cholesterol carrier in the brain . As a group, these individuals have higher plasma LDL concentrations, compared with APOEε3 homozygotes  Moreover, APOE status may influence the relationship between dietary intake and plasma lipid concentrations . APOE determination may provide useful information as to who benefits from dietary changes that aim to modify plasma lipid concentrations, with implications for subsequent risk of cardiovascular disease and Alzheimer's disease. The blood test will be drawn once, at the 20-week health assessment only. This test will be optional. If participants decide not to do the test, it will not affect their status in the study. The blood samples that are collected will be used for APOE allele testing for this study only. All samples will be destroyed after analysis and no part of the specimen will be retained per policy of Quest Diagnostics.
Genotyping for Taq1 A and Taq1B polymorphisms. Participants who consent to this aspect of the study will be genotyped for the A1 and B1 alleles, using the PCR method  A sample of approximately 5 ml of the participant's blood is required and will be drawn simultaneously with the 20-week health assessment labs. Studies suggest that the A1 allele of the Taq1A polymorphism (rs1800497), located ≈10 kb downstream of the D2 dopamine receptor (DRD2) gene, may influence dietary behavior and response to treatment. Individuals with the A1 allele generally have a lower-than-normal complement of dopamine receptors (DRD2) in the human brain, and are more likely than others to engage in smoking, substance abuse, and compulsive gambling . The prevalence of A1 and B1 alleles of the DRD2 gene is strongly associated with severe alcoholism . Further, the A1 allele is also common among obese individuals . We identified this allele in approximately half of individuals with type 2 diabetes participating in a research study . The possibility that genetic factors may influence dietary behavior may mean that extended support is essential for facilitating dietary transitions among many, if not all, individuals with diabetes. In group settings, support can be engaging and cost effective. The blood test will be drawn once, at the 20-week health assessment only. This test will be optional. If participants decide not to do the test, it will not affect their status in the study. The blood samples that are collected will be used for TaqA1 allele testing for this study only. All samples will be destroyed after analysis and no part of the specimen will be retained per policy of The Biological Samples Processing Core Facility (BSPC) at the University of California, Los Angeles (UCLA).
All participants will undergo assessment of peripheral autonomic neuropathy via SUDOSCAN testing. SUDOSCAN is an FDA cleared device to assess Galvanic Skin Response (Sudoscan has 510(k) clearance, which is a premarketing submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent (SE), to a legally marketed device that is not subject to premarket approval). Previous work has shown that galvanic skin response is a promising, sensitive, simple tool for detecting diabetic neuropathy, because the production of perspiration depends on the presence of functional small nerve fibers. One study of 83 diabetic patients and 210 healthy controls showed that the Sudoscan measurement showed a sensitivity of 78% and a specificity of 92%, which is as good as or better than clinical evaluation methods.48 In addition, test-retest reliability is very high, especially for the feet.49 A study of 167 type 1 and type 2 diabetics showed that galvanic skin response improved after 1 year of intense insulin therapy.49 This method is appropriate for inclusion in this study because it is a non-invasive, objective way to assess neurological function. Participants will place both palms and soles on large area stainless-steel electrodes and stand still for the 3-minute scan. A low voltage (<4V) is applied incrementally to the electrodes, generating a current (around 0.2mA) proportional to the chloride ions in the sweat glands of the palms and soles. The electrochemical skin conductance measured in microSiemens for each foot and each hand will be recorded by the SUDOSCAN.
2-day dietary record: A 2-day dietary record will be used to assess macro- and micronutrient intakes. Participants will be given the option to complete a manual or online version (online: http://riskfactor.cancer.gov/tools/instruments/asa24/) for collecting and calculating diet and nutrient intake. Participants will need Internet access if they choose to do an online version. If necessary, digitized records will be analyzed using Nutrition Data Systems for Research software (University of Minnesota), by a registered dietitian certified by the Nutrition Coordinating Center.
24-Hour Multi-Pass Dietary Recalls. At weeks 3 and 12, a registered dietitian will make unannounced telephone calls to each participant to administer a 24-hour diet recall, using a multi-pass approach (Nutrition Coordinating Center, University of Minnesota, Minneapolis, MN). These recalls will not be subjected to statistical analysis, but will allow the investigators to check for poor adherence. The ASA-24 is a software tool developed by National Cancer Institute. It enables automated and self-administered 24-hour dietary recalls. The format and design of ASA-24 are based on a modified version of the interviewer-administered Automated Multiple Pass Method (AMPM) 24-hour recall developed by the U.S. Department of Agriculture. Participants will be provided a user name, password, and link to the ASA-24 online diet recall Web site.
The Eating Inventory is a highly reliable 51-item questionnaire providing quantitative measures of dietary restraint, disinhibition, and hunger. It will serve as a gauge of ease in adapting to the intervention diet.
The International Physical Activity Questionnaire short form assesses recent physical activity patterns. The method is highly reliable; an assessment of test-retest repeatability produced a correlation of 0.8.
The Clinical Epidemiologic Studies Depression Scale-Revised (CESD-R) assesses mood. The CES-D is a 20-item self-report measure designed originally for use among the general population. It measures the frequency with which participants have experienced a specific symptom within the preceding week, using a four-point rating scale.
The Beck Depression Inventory II (BDI-II) assesses mood. It is the most widely used instrument for detecting depression. The questions on the BDI-II are in alignment with DSM-IV criteria. Each item is a list of four statements arranged in increasing severity about a particular symptom of depression.
Overall quality of life will be assessed using the SF-36, which is a brief health survey with 36 questions. The SF-36 provides psychometrically-based physical and mental health summary measures. The SF-36 is a general measure that has been administered across various age groups, disease spectra, and treatment regimens. Items on the SF-36 are scored on a scale of 0-100, with a higher score indicating better health-related quality of life.
Medications. Participants in both groups will be asked to keep their medications constant and to add no new nutritional supplements to their current medication regimen, except as recommended by their personal physicians.
The interventions for the diet and supplement group and supplement-only group are described below:
The diet and supplement group will be asked to follow a low-fat, vegan diet and take a daily vitamin B12 supplement of 1000mcg of methylcobalamin for 20 weeks. According to the American Dietetic Association, vegan and vegetarian diets meet all nutritional requirements when appropriately planned.The diet consists of whole grains, vegetables, legumes, and fruits, with no restriction on energy intake. Animal products, added oils, and sugars will be excluded. In choosing grain products and starchy vegetables (e.g., bread, potatoes), participants will be encouraged to select those retaining their natural fiber and having a glycemic index <70, using tables standardized to a value of 100 for glucose. No meals will be provided. Participants will handle their own food preparation and purchases, with guidance from the research team.
Participants will be provided with a commercially available supplement containing vitamin B12 and asked to take it daily during the study. Should they wish to continue the diet thereafter, they will be counseled to use any standard multivitamin or other reliable source of vitamin B12.
The supplement-only group will follow an unrestricted diet, but will be given the identical vitamin B12 supplement of 1000mcg of methylcobalamin as the diet group.
Before randomization, participants will be told that they will either be assigned to a diet and supplement intervention group or a supplement-only group.
For both groups, alcoholic beverages will be limited to one per day for women, and two for men.
|Study Type ICMJE||Interventional|
|Study Phase ICMJE||Not Applicable|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
|Condition ICMJE||Diabetic Neuropathy|
|Study Arms ICMJE||
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Completed|
|Actual Enrollment ICMJE
|Original Estimated Enrollment ICMJE
|Actual Study Completion Date ICMJE||March 2015|
|Actual Primary Completion Date||March 2015 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages ICMJE||18 Years to 65 Years (Adult, Older Adult)|
|Accepts Healthy Volunteers ICMJE||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||United States|
|Removed Location Countries|
|NCT Number ICMJE||NCT01953757|
|Other Study ID Numbers ICMJE||PCRM DN-2|
|Has Data Monitoring Committee||Yes|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement ICMJE||Not Provided|
|Responsible Party||Physicians Committee for Responsible Medicine|
|Study Sponsor ICMJE||Physicians Committee for Responsible Medicine|
|Collaborators ICMJE||Not Provided|
|PRS Account||Physicians Committee for Responsible Medicine|
|Verification Date||April 2015|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP