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Wahls Paleo Diet and Progressive Multiple Sclerosis

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Wahls Paleo Plus
Wahls Diet
Sponsored by
Terry L. Wahls
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Secondary Progressive Multiple Sclerosis, Primary Progressive Multiple Sclerosis, Relapsing progressive multiple sclerosis, relapsing remitting multiple sclerosis, Fatigue, Quality of life, Paleo, Nutrition, Ketogenic

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria - to complete 2 week RUN IN to determine eligibility for Main Study:

Inclusion Criteria -

  1. Secondary or Primary Progressive MS, relapsing progressive MS, relapsing- remitting MS
  2. Generally able to walk 25 feet in less than 60 seconds;
  3. significant fatigue as documented by a fatigue severity scale score of 4 or more OR a modified fatigue impact scale score of 38 or higher.
  4. age between 30 and including 65 at entry into the RUN IN study,
  5. non smoker,
  6. willingness to be randomized
  7. Mild gait disability as shown by an EDSS score of 4.5 or higher
  8. Confirmed MS diagnosis using McDonald criteria
  9. Eating standard American diet.

Exclusion Criteria for RUN IN to determine eligibility:

  1. change in medication in the prior 90 days, taking anti-platelet or anticoagulant therapy therapy, or having a major psychiatric disorder making compliance difficult,
  2. SELF REPORTED history of current diagnosis of diabetes, or active liver, kidney or clinically significant heart disease,
  3. unable to record daily weight at home,
  4. eating a vegetarian diet or chronic diarrhea, have already adopted a Paleo Diet (as defined by a complete elimination of grain, dairy, and legumes)
  5. unable to cope with 30% in grocery bill,
  6. Alanine aminotransferase value > 2X normal, or elevated creatinine value, (main study only)
  7. incompetence.
  8. Too low or too high BMI.
  9. Inability to follow study diet, which requires shopping carefully and food preparation, by either the study subject or with the help of an adult companion to do the shopping and food preparation.
  10. aversion to coconut milk

Main Study Inclusion Criteria

1) Successful completion of RUN IN Study - which means, the subject completed the various quest. and survey documents that are part of the RUN-IN study, completed the food diary for each day they participated in the RUN-IN, the subject is eating the standard American Diet as documented by the daily food logs and the 24 hour dietary recalls.

Sites / Locations

  • Univeristy of Iowa
  • Univeristy of Iowa

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Wahls Paleo Plus

Wahls Diet

Usual Care

Arm Description

Wahls Paleo Plus diet (ketogenic diet)

Wahls Diet (modified paleolithic diet)

Control - usual care only.

Outcomes

Primary Outcome Measures

Perceived Fatigue
Fatigue as measured by the fatigue severity scale and the modified fatigue impact scale

Secondary Outcome Measures

Biomarkers
Biomarkers include weight, Body Mass Index,and blood biomarkers of renal and liver function, vitamin levels (A,C,K,D, B vitamins), homocysteine, h.s. c- reactive protein (CRP)
Biomarkers - glucose and ketones
GLucose, insulin, ketones, hemoglobin a1c to assess insulin sensitivity. Full intervention at baseline, and weeks 4,8,12 Minimal intervention at baseline and week 12.
24 hr food recalls.
The 24 hr recalls will be collected at baseline in in the last 4 weeks of study. This will include nutrient analyses as well.
Daily Food logs
This is a record of daily food and beverage consumption. The two intervention groups will keep the record daily. The usual care group will keep the a food record the initial two weeks and for two weeks between weeks 10 and 12.
MS functional composite score.
This a composite of tests involving tests of walking, hand coordination and mental addition.
6 minute walk test
Subject will walk 6 minutes. They may rest as needed during the 6 minute time period. The total length of time that is walked will be recorded.
Medical symptoms quest. (MSQ)
Scored review of systems questionaire
Life spaces score
Questions about the locations subjects has been in the prior time period of interest.
Medication audit
List of currently used medications, vitamins, supplements and over the counter medications.
Physical examination
Summary of physical findings from physical examination.
Health questions
A list of questions to identify common medical comorbid conditions and their severity if present.
MS Quality of Life (MSQoli 54)
MS Qoli 54 is a series of questions about physical function, role limitations-physical, role limitations-emotional, pain, emotional well-being, energy, health perceptions, social function, cognitive function, health distress, overall quality of life.
MS Quality of life inventory (MSQLI)
MSQLI is a series of questions asking about daily life. Includes physical function, role limitations-physical, role limitations-emotional, pain, emotional well-being, energy, health perceptions, social function, cognitive function, health distress, overall quality of life.
Demographic data
Questions about demographic attributes such as race, education, handedness.
Functional Medicine assessment summary
A series of questions about a number of environmental risk factors for development of neurological and medical symptoms. Completed prior to orientation to study intervention diet after randomization (intervention groups) or at 12 weeks for usual care group.
Veteran Specific Activity Quest.
Series of questions about the tasks of daily life to identify how much activity the individual can safely do.
MS Function Scale
A series of questions about the tasks of daily life.
Satiety scale
A series of questions about the sense of satiety or sense of fullness.
Harvard Food Frequency Quest.
A series of questions about the frequency of a variety of foodstuffs to estimate nutrient intake.
Brachial artery dilation (FMD)and endothelium-dependent dilation, EDD) and endothelium-independent dilation
Brachial artery FMD and endothelium-independent dilation will be determined non-invasively using high-resolution ultrasonography.
Expanded disability status score
Assessment of disability status

Full Information

First Posted
July 25, 2013
Last Updated
June 22, 2018
Sponsor
Terry L. Wahls
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1. Study Identification

Unique Protocol Identification Number
NCT01915433
Brief Title
Wahls Paleo Diet and Progressive Multiple Sclerosis
Official Title
Wahls Paleo Diet and Progressive Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Terry L. Wahls

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Based on favorable preliminary data from ongoing studies testing the safety and tolerability of a nutrition, exercise and neuromuscular electrical stimulation funded by Direct MS, the investigators are proposing a pilot study focused on the Wahls Paleo plus Diet and Wahls Diet intervention to usual care. The intent is to measure the effect size of a Wahls Paleo plus Diet and the effect size of the Wahls Diet in reducing fatigue and improving quality of life scores as measured by fatigue severity scale score and MS quality of life 54 physical and mental scores and various subscale scores. Inclusion criteria is the presence of fatigue and the diagnosis secondary and primary progressive MS, progressive relapsing MS or relapsing-remitting MS with an expanded disability status scale score (EDSS) score of 4.5 or greater but otherwise stable medically. The Wahls Paleo plus (ketogenic diet) and the Wahls diet (modified paleolithic diet) groups will be instructed in completing a daily food log and receive coaching from registered dieticians who are expert in motivational interviewing. The control group will receive usual care. Biomarkers of nutrient levels (e.g. vitamin) and inflammation, blood sugar and insulin levels will be monitored. Additional blood will be frozen for future analysis. Nutrient (e.g. vitamin and antioxidant) intake will be assessed using food frequency questionnaires and 24 hr diet recalls. Test of endothelial function will be done at baseline and 12 weeks. Outcome measures will be change in quality of life and fatigue, endothelial function and blood biomarkers between enrollment and end of study at 12 weeks. The hypotheses are that the diet intervention groups will experience reduced fatigue and improved quality of life and improved biomarkers 1) between zero and 12 weeks and that the wahls paleo plus (ketogenic diet) and the wahls diet (modified paleolithic diet) groups will experience more improvements in quality of life and reduced fatigue and in biomarkers than the usual care group experiences at 12 weeks. The usual care group will be given instruction in following both the wahls paleo plus and the wahls diet plans and how to utilize the daily food logs at the end of study visit. The usual care group will receive one nutrition coaching call to assist with implementation of the study diet.
Detailed Description
Specific Aim 1. To assess changes in fatigue severity (primary outcome measure) and quality of life, motor, cognitive and emotional functions (secondary measures) the intervention groups (wahls paleo plus and wahls diet group)to usual care. Hypothesis 1a: The Wahls Paleo plus group and the wahls diet group will both demonstrate more improvements in quality of life and fatigue between baseline and 12 weeks than usual care group. Hypothesis 1b. The wahls paleo plus group will demonstrate more improvement in quality of life and fatigue than the wahls diet group. Specific Aim 2. To assess changes in the blood biomarkers and endothelial function as the subject progresses through the study interventions. Hypothesis 2a: The wahls paleo plus and the wahls diet group will demonstrate more favorable changes in blood biomarkers obtained at baseline and week 12 than the usual care group. Hypothesis 2b: The wahls paleo plus group will demonstrate more favorable changes in blood biomarkers and quality of life than the wahls diet group experiences obtained at baseline and week 12. Hypothesis 2c: The wahls paleo plus and the wahls diet group will demonstrate more favorable changes in measures of endothelial function between baseline and week 12 than will be observed in the usual care group. Hypothesis 2d: The wahls paleo plus will demonstrate more favorable changes in measures of endothelial function between baseline and week 12 than the wahls diet group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Secondary Progressive Multiple Sclerosis, Primary Progressive Multiple Sclerosis, Relapsing progressive multiple sclerosis, relapsing remitting multiple sclerosis, Fatigue, Quality of life, Paleo, Nutrition, Ketogenic

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Wahls Paleo Plus
Arm Type
Experimental
Arm Description
Wahls Paleo Plus diet (ketogenic diet)
Arm Title
Wahls Diet
Arm Type
Experimental
Arm Description
Wahls Diet (modified paleolithic diet)
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Control - usual care only.
Intervention Type
Other
Intervention Name(s)
Wahls Paleo Plus
Other Intervention Name(s)
Wahls Paleo Plus (ketogenic diet)
Intervention Description
The study diet is based upon a Paleolithic Diet, also known as a Hunter Gatherer Diet, which exceeds the recommended daily allowance of water soluble vitamins and minerals 1.5 to 8 fold and improves lipids, inflammatory biomarkers and blood pressure. The study diet is further structured to be a low in carbohydrate and high in fat but still ensure consumption of the specific micronutrients important to optimal brain function. This diet is designed to induce a low level nutritional ketosis.
Intervention Type
Other
Intervention Name(s)
Wahls Diet
Other Intervention Name(s)
Wahls Diet (modified paleolithic diet)
Intervention Description
The study diet is based upon a Paleolithic Diet, also known as a Hunter Gatherer Diet, which exceeds the recommended daily allowance of water soluble vitamins and minerals 1.5 to 8 fold and improves lipids, inflammatory biomarkers and blood pressure. The study diet is further structured to be a low glycemic diet and also ensure consumption of the specific micronutrients important to optimal brain function.
Primary Outcome Measure Information:
Title
Perceived Fatigue
Description
Fatigue as measured by the fatigue severity scale and the modified fatigue impact scale
Time Frame
Baseline, weeks, 4,8 and 12
Secondary Outcome Measure Information:
Title
Biomarkers
Description
Biomarkers include weight, Body Mass Index,and blood biomarkers of renal and liver function, vitamin levels (A,C,K,D, B vitamins), homocysteine, h.s. c- reactive protein (CRP)
Time Frame
Baseline and 12 weeks
Title
Biomarkers - glucose and ketones
Description
GLucose, insulin, ketones, hemoglobin a1c to assess insulin sensitivity. Full intervention at baseline, and weeks 4,8,12 Minimal intervention at baseline and week 12.
Time Frame
Baseline and at 4, 8, 12 weeks
Title
24 hr food recalls.
Description
The 24 hr recalls will be collected at baseline in in the last 4 weeks of study. This will include nutrient analyses as well.
Time Frame
Baseline and 12 weeks
Title
Daily Food logs
Description
This is a record of daily food and beverage consumption. The two intervention groups will keep the record daily. The usual care group will keep the a food record the initial two weeks and for two weeks between weeks 10 and 12.
Time Frame
Baseline through end of study (12 weeks)
Title
MS functional composite score.
Description
This a composite of tests involving tests of walking, hand coordination and mental addition.
Time Frame
Baseline and end of study (12 weeks)
Title
6 minute walk test
Description
Subject will walk 6 minutes. They may rest as needed during the 6 minute time period. The total length of time that is walked will be recorded.
Time Frame
Baseline and week 12
Title
Medical symptoms quest. (MSQ)
Description
Scored review of systems questionaire
Time Frame
Baseline, weekly through week 12
Title
Life spaces score
Description
Questions about the locations subjects has been in the prior time period of interest.
Time Frame
Baseline and week 12
Title
Medication audit
Description
List of currently used medications, vitamins, supplements and over the counter medications.
Time Frame
Baseline
Title
Physical examination
Description
Summary of physical findings from physical examination.
Time Frame
baseline and 12 weeks
Title
Health questions
Description
A list of questions to identify common medical comorbid conditions and their severity if present.
Time Frame
baseline
Title
MS Quality of Life (MSQoli 54)
Description
MS Qoli 54 is a series of questions about physical function, role limitations-physical, role limitations-emotional, pain, emotional well-being, energy, health perceptions, social function, cognitive function, health distress, overall quality of life.
Time Frame
Baseline, week 12
Title
MS Quality of life inventory (MSQLI)
Description
MSQLI is a series of questions asking about daily life. Includes physical function, role limitations-physical, role limitations-emotional, pain, emotional well-being, energy, health perceptions, social function, cognitive function, health distress, overall quality of life.
Time Frame
Baseline and week 12
Title
Demographic data
Description
Questions about demographic attributes such as race, education, handedness.
Time Frame
Baseline and week 12
Title
Functional Medicine assessment summary
Description
A series of questions about a number of environmental risk factors for development of neurological and medical symptoms. Completed prior to orientation to study intervention diet after randomization (intervention groups) or at 12 weeks for usual care group.
Time Frame
Baseline or 12 weeks
Title
Veteran Specific Activity Quest.
Description
Series of questions about the tasks of daily life to identify how much activity the individual can safely do.
Time Frame
Baseline and 12 weeks.
Title
MS Function Scale
Description
A series of questions about the tasks of daily life.
Time Frame
baseline and week 12
Title
Satiety scale
Description
A series of questions about the sense of satiety or sense of fullness.
Time Frame
Baseline and weeks 10 and 11
Title
Harvard Food Frequency Quest.
Description
A series of questions about the frequency of a variety of foodstuffs to estimate nutrient intake.
Time Frame
Baseline
Title
Brachial artery dilation (FMD)and endothelium-dependent dilation, EDD) and endothelium-independent dilation
Description
Brachial artery FMD and endothelium-independent dilation will be determined non-invasively using high-resolution ultrasonography.
Time Frame
Baseline and week 12
Title
Expanded disability status score
Description
Assessment of disability status
Time Frame
Baseline and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria - to complete 2 week RUN IN to determine eligibility for Main Study: Inclusion Criteria - Secondary or Primary Progressive MS, relapsing progressive MS, relapsing- remitting MS Generally able to walk 25 feet in less than 60 seconds; significant fatigue as documented by a fatigue severity scale score of 4 or more OR a modified fatigue impact scale score of 38 or higher. age between 30 and including 65 at entry into the RUN IN study, non smoker, willingness to be randomized Mild gait disability as shown by an EDSS score of 4.5 or higher Confirmed MS diagnosis using McDonald criteria Eating standard American diet. Exclusion Criteria for RUN IN to determine eligibility: change in medication in the prior 90 days, taking anti-platelet or anticoagulant therapy therapy, or having a major psychiatric disorder making compliance difficult, SELF REPORTED history of current diagnosis of diabetes, or active liver, kidney or clinically significant heart disease, unable to record daily weight at home, eating a vegetarian diet or chronic diarrhea, have already adopted a Paleo Diet (as defined by a complete elimination of grain, dairy, and legumes) unable to cope with 30% in grocery bill, Alanine aminotransferase value > 2X normal, or elevated creatinine value, (main study only) incompetence. Too low or too high BMI. Inability to follow study diet, which requires shopping carefully and food preparation, by either the study subject or with the help of an adult companion to do the shopping and food preparation. aversion to coconut milk Main Study Inclusion Criteria 1) Successful completion of RUN IN Study - which means, the subject completed the various quest. and survey documents that are part of the RUN-IN study, completed the food diary for each day they participated in the RUN-IN, the subject is eating the standard American Diet as documented by the daily food logs and the 24 hour dietary recalls.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Terry L Wahls, MD
Organizational Affiliation
University of Iowa
Official's Role
Study Director
Facility Information:
Facility Name
Univeristy of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52240
Country
United States
Facility Name
Univeristy of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52246
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21138391
Citation
Wahls TL, Reese D, Kaplan D, Darling WG. Rehabilitation with neuromuscular electrical stimulation leads to functional gains in ambulation in patients with secondary progressive and primary progressive multiple sclerosis: a case series report. J Altern Complement Med. 2010 Dec;16(12):1343-9. doi: 10.1089/acm.2010.0080.
Results Reference
background
PubMed Identifier
19918474
Citation
Reese D, Shivapour ET, Wahls TL, Dudley-Javoroski SD, Shields R. Neuromuscular electrical stimulation and dietary interventions to reduce oxidative stress in a secondary progressive multiple sclerosis patient leads to marked gains in function: a case report. Cases J. 2009 Aug 10;2:7601. doi: 10.4076/1757-1626-2-7601.
Results Reference
background
PubMed Identifier
21253878
Citation
Wahls TL. The seventy percent solution. J Gen Intern Med. 2011 Oct;26(10):1215-6. doi: 10.1007/s11606-010-1631-3. No abstract available.
Results Reference
background
PubMed Identifier
21827937
Citation
Riccio P. The molecular basis of nutritional intervention in multiple sclerosis: a narrative review. Complement Ther Med. 2011 Aug;19(4):228-37. doi: 10.1016/j.ctim.2011.06.006. Epub 2011 Jul 27.
Results Reference
background
PubMed Identifier
17066210
Citation
Bourre JM. Effects of nutrients (in food) on the structure and function of the nervous system: update on dietary requirements for brain. Part 2 : macronutrients. J Nutr Health Aging. 2006 Sep-Oct;10(5):386-99.
Results Reference
background
PubMed Identifier
17066209
Citation
Bourre JM. Effects of nutrients (in food) on the structure and function of the nervous system: update on dietary requirements for brain. Part 1: micronutrients. J Nutr Health Aging. 2006 Sep-Oct;10(5):377-85.
Results Reference
background
PubMed Identifier
22205763
Citation
Bowman GL, Silbert LC, Howieson D, Dodge HH, Traber MG, Frei B, Kaye JA, Shannon J, Quinn JF. Nutrient biomarker patterns, cognitive function, and MRI measures of brain aging. Neurology. 2012 Jan 24;78(4):241-9. doi: 10.1212/WNL.0b013e3182436598. Epub 2011 Dec 28.
Results Reference
background
PubMed Identifier
19209185
Citation
Frassetto LA, Schloetter M, Mietus-Synder M, Morris RC Jr, Sebastian A. Metabolic and physiologic improvements from consuming a paleolithic, hunter-gatherer type diet. Eur J Clin Nutr. 2009 Aug;63(8):947-55. doi: 10.1038/ejcn.2009.4. Epub 2009 Feb 11. Erratum In: Eur J Clin Nutr. 2015 Dec;69(12):1376.
Results Reference
background
PubMed Identifier
22509165
Citation
Stafstrom CE, Rho JM. The ketogenic diet as a treatment paradigm for diverse neurological disorders. Front Pharmacol. 2012 Apr 9;3:59. doi: 10.3389/fphar.2012.00059. eCollection 2012.
Results Reference
background

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Wahls Paleo Diet and Progressive Multiple Sclerosis

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