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Study to Evaluate Coconut Oil for Alzheimer's Disease

This study is currently recruiting participants. (see Contacts and Locations)
Verified August 2015 by University of South Florida
Sponsor:
Information provided by (Responsible Party):
University of South Florida
ClinicalTrials.gov Identifier:
NCT01883648
First received: June 11, 2013
Last updated: September 16, 2015
Last verified: August 2015
  Purpose
This is a randomized, cross over study to determine the efficacy of coconut oil in subjects with mild to moderate Alzheimer's disease.

Condition Intervention Phase
Alzheimer's Disease
Drug: Coconut Oil Beverage
Other: Placebo Beverage
Phase 2
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Randomized, Double-Blind, Placebo-Controlled, 6 Month Cross-Over Study to Evaluate the Efficacy of Coconut Oil (Fuel for Thought™) Treatment for Subjects With Mild to Moderate Alzheimer's Disease

Resource links provided by NLM:


Further study details as provided by University of South Florida:

Primary Outcome Measures:
  • Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in cognitive testing (ADAS-cog, MMSE, Category/Letter Fluency) [ Time Frame: Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in cognitive testing (ADAS-cog, MMSE, Category/Letter Fluency) ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in Trails A & B cognitive testing [ Time Frame: Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in Trails A & B cognitive testing ] [ Designated as safety issue: No ]
  • Change from baseline to Month 3 of each treatment phase (a 3 month period of time) on Geriatric Depression Scale [ Time Frame: Change from baseline to Month 3 of each treatment phase (a 3 month period of time) on Geriatric Depression Scale ] [ Designated as safety issue: No ]
  • Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in behaviors measured by Neuropsychiatric Inventory [ Time Frame: Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in behaviors measured by Neuropsychiatric Inventory ] [ Designated as safety issue: No ]
  • Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in functional ability measured by Activities of Daily Living (ADCS-ADLs) [ Time Frame: Change from baseline to Month 3 of each treatment phase (a 3 month period of time) in functional ability measured by Activities of Daily Living (ADCS-ADLs) ] [ Designated as safety issue: No ]
  • Measure changes in Ketone & C-Reactive Protein assays from research blood samples throughout study during the 2 treatment periods from Baseline to Month 6 (change during a total 6 month period of time). [ Time Frame: Measure changes in Ketone & C-Reactive Protein assays from research blood samples throughout study during the 2 treatment periods from Baseline to Month 6 (change during a total 6 month period of time). ] [ Designated as safety issue: No ]
  • Adverse events related to coconut oil usage during 6 months of treatment periods (change during a total 6 month period of time). [ Time Frame: Adverse events related to coconut oil usage during 6 months of treatment periods (change during a total 6 month period of time). ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 65
Study Start Date: June 2013
Estimated Study Completion Date: June 2017
Estimated Primary Completion Date: December 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Coconut Oil Beverage
The treatment will consist of a 1.25 oz serving size taken orally, two times daily by subjects. This treatment arm will last 3 months.
Drug: Coconut Oil Beverage
There are 2 treatment arms: Fuel for Thought™ and placebo, with a treatment allocation of 1:1. After 3 months of treatment in one group, subjects will have a 3-5 day wash-out period before receiving the alternate (opposite) treatment for 3 months.
Other Name: Fuel for Thought (TM)
Placebo Comparator: Placebo Beverage
The treatment will consist of a 1.25 oz serving size taken orally, two times daily by subjects.This will similar in look and taste but not have the same ingredients of the actual coconut oil beverage. This treatment arm will last 3 months.
Other: Placebo Beverage
There are 2 treatment arms: Fuel for Thought™ and placebo, with a treatment allocation of 1:1. After 3 months of treatment in one group, subjects will have a 3-5 day wash-out period before receiving the alternate (opposite) treatment for 3 months.

Detailed Description:

This is a randomized, double-blind, placebo-controlled, cross over study to determine the efficacy of coconut oil (a proprietary blend of coconut and medium chain triglyceride oils, administered orally three times daily) to subjects with Alzheimer's disease who have been screened for ApoE 4 allele. The study medication formula is Cognate Nutritionals Fuel for Thought™.

Approximately 65 subjects will be treated with a coconut oil beverage (Fuel for Thought™) or placebo for three months, and then given a 3-5 day interim wash out period. After this, subjects will resume with three months treatment in opposite treatment arm. Total treatment period is 6 months.

  Eligibility

Ages Eligible for Study:   55 Years to 90 Years   (Adult, Senior)
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Men and women aged 55 to 90 years with a diagnosis of mild to moderate Alzheimer's disease
  • Informed consent signed and dated by subject (or legally authorized representative).
  • Subjects must have a study partner must also consent to participate in the study, who they spend at least 10 hours/week with during the study. The study partner must attend applicable clinic visits and provide information about the subject.
  • Subject must have a screening Mini-Mental State Examination score of 16-26.
  • Subjects must have a Rosen Modified Hachinski Ischemic score of ≤4.
  • Subject must undergo ApoE genetic laboratory testing at the baseline visit.
  • Subject must be willing and able to take study medication (or placebo) for the duration of the study.
  • Subject must be stable on all memory enhancing medications including cholinesterase inhibitors (including donepezil, rivastigmine, and galantamine) and NMDA antagonist (memantine) for at least 3 months prior to screening and agree not to change these medications during the course of their participation, unless medically necessary.
  • Subject must be stable on all memory enhancing nonprescription supplements (including gingko biloba, huperzine, resveratrol, or docosahexaenoic acid) for at least 3 months prior to screening and agree not to change these medications during the course of their participation.
  • As judged by Investigator, the subject and study partner will be compliant and have a high probability of completing the study, including all scheduled evaluations and required tests.
  • Be fluent in English.

Exclusion Criteria:

  • Has significant neurological or medical disease, other than AD, that may affect cognition, for example, history or evidence of hydrocephalus, or uncontrolled hypo- or hyperthyroidism.
  • Current, clinically significant major psychiatric disorder (eg, major depressive disorder) according to the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSMIV), or symptoms (eg, hallucinations) that could affect the subject's ability to complete the study.
  • Geriatric depression scale score of more than 6 or has suicidal ideation.
  • Current clinically significant chronic illness that is likely to result in deterioration of the subject's condition or affect the subject's safety during the study, including uncontrolled diabetes. Subjects with a history of diabetic ketoacidosis will also be excluded. Other cases of diabetes will be decided at the discretion of the study physicians. Subjects with diabetes controlled with exercise and diet may be screened and admission to study will depend on their screening safety laboratory assessments.
  • History of clinically evident stroke or history of clinically significant carotid or vertebrobasilar stenosis or plaque and other risk factors for thromboembolic stroke (e.g atrial fibrillation, clinically significant low ventricular output, atrial septal defect).
  • History of seizures.
  • Clinically significant infection within the last 30 days (eg, chronic persistent or acute infection [eg, upper respiratory infection, urinary tract infection]),prior to screening.
  • Myocardial infarction within the last 2 years.
  • Abnormal screening visit electrocardiogram (ECG), in the opinion of the investigator.
  • Uncontrolled hypertension within the last 6 months prior to screening.
  • History of cancer within the last 3 years, with the exception of nonmetastatic basal cell carcinoma and squamous cell carcinoma of the skin. (Note: cancer must be in remission with no signs of progression.)
  • Use of experimental or other investigational medications/devices for treatment within 90 days prior to screening.
  • Laboratory findings of fasting total cholesterol greater than or equal to 240 mg/dL
  • Laboratory findings of fasting triglycerides greater than or equal to 200 mg/dL
  • Laboratory findings of fasting glucose greater than or equal to 126 mg/dL
  • Other clinically significant abnormality on physical, neurological, laboratory, vital signs, or ECG examination (eg, changes consistent with recent infarction, ischemia, clinically significant arrhythmias and clinically significant conduction defects) that could be detrimental to the subject or compromise the study.
  • Does not have adequate venous access that would allow blood draws.
  • Subject or study partner is related to study personnel.
  • Subjects who have taken coconut oil as a supplement within the last 30 days.
  • Subjects who have taken Axona™ within the last 30 days.
  • Women who are pregnant. (Women who are of child bearing potential must take precautions to not become pregnant during the study.)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01883648

Locations
United States, Florida
USF Health Byrd Alzheimer's Institute Recruiting
Tampa, Florida, United States, 33613
Contact: Jill Smith, MA, CCRC    813-974-4355    jsmith10@health.usf.edu   
Principal Investigator: Amanda G Smith, MD         
Sub-Investigator: Balebail A Raj, MD         
Sponsors and Collaborators
University of South Florida
Investigators
Principal Investigator: Amanda G Smith, MD USF Health Byrd Alzheimer's Institute
  More Information

Additional Information:
Responsible Party: University of South Florida
ClinicalTrials.gov Identifier: NCT01883648     History of Changes
Other Study ID Numbers: Byrd AD-001 
Study First Received: June 11, 2013
Last Updated: September 16, 2015
Health Authority: United States: Food and Drug Administration

Keywords provided by University of South Florida:
Mild to Moderate Alzheimer's disease

Additional relevant MeSH terms:
Alzheimer Disease
Dementia
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Tauopathies
Neurodegenerative Diseases
Neurocognitive Disorders
Mental Disorders

ClinicalTrials.gov processed this record on September 23, 2016