search
Back to results

Fish Oil and Alpha Lipoic Acid in Treating Alzheimer's Disease

Primary Purpose

Alzheimer's Disease, Oxidative Stress, Dementia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Fish Oil
Lipoic Acid
Fish Oil Placebo
Lipoic Acid Placebo
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer's Disease focused on measuring Fish Oils, Thioctic Acid, Antioxidants, Dietary Supplements

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of probable Alzheimer's Disease or mild cognitive impairment Mini Mental State Examination (MMSE) score between 18 and 26 Clinical Dementia Rating (CDR) of 0.5 or 1.0 Fluent in English Exclusion Criteria: Use of lipid lowering medications Consumption of fish of more than twice a week Use of omega and alpha lipoic acid supplements Use of systemic corticosteroids, neuroleptics, anti-Parkinsonian agents, or narcotic analgesics Depression Any other serious health conditions that may interfere with the study Enrollment in another clinical trial

Sites / Locations

  • Oregon Health and Science University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Active Comparator

Experimental

Arm Label

Fish Oil Placebo & Lipoic Acid Placebo

Fish Oil Only

Fish Oil Plus Lipoic Acid

Arm Description

Three 1-gram placebo-fish oil capsules (2 in the morning, 1 evening) plus one 600 milligram placebo-lipoic acid per day. Placebo fish oil capsules consisted of soybean oil flavored with lemon flavor and 5% fish oil to match fish oil capsules. LA placebo contained no LA and the following excipients: lactose, hypromellose, silicon dioxide, microcrystalline cellulose, polyethylene glycol, povidone, corn starch, talc, and magnesium stearate.

Three 1-gram fish oil concentrate capsules in triglyceride form (675 milligrams DHA and 975 milligrams EPA), 2 in the morning and 1 in the evening, plus one 600 milligram placebo-lipoic acid (containing no LA and the following excipients: lactose, hypromellose, silicon dioxide, microcrystalline cellulose, polyethylene glycol, povidone, corn starch, talc, and magnesium stearate) per day.

Three 1-gram placebo-fish oil capsules (2 in the morning, 1 evening) plus one 600 milligram lipoic acid (LA) capsule in the racemic form per day.

Outcomes

Primary Outcome Measures

F2-isoprostane Level Urine F2-Isoprostanes
F2-isoprostane is a biomarker was used as an effective indicator for detecting a decrease in systemic oxidative damage (oxidative damage in lipids). Urine F2-Isoprostanes were used to avoid ex vivo lipid peroxidation that can occur with plasma samples.
Change in Mini-Mental State Exam (MMSE) Score From Baseline to 12 Months
The MMSE is a measure of global cognitive function, and scores range from 0-30, with a lower score indicates greater cognitive impairment.

Secondary Outcome Measures

Change in Activities of Daily Living/Instrumental Activities of Daily Living (ADL/IADL) Scores From Baseline to 12 Months
The Activities of Daily Living/Instrumental Activities of Daily Living (ADL/IADL) measures an individual's ability to carry out tasks that are important for daily living and capture functional changes. Scores for each question range from 0 (no assistance needed) to 2 (full assistance needed), and were assessed by informant interview. The combination of scores for ADL (ranging from 0-18) and IADL (0-14) is the outcome (0-32), with higher scores indicating lesser ability to carry out daily living tasks.

Full Information

First Posted
August 25, 2004
Last Updated
June 21, 2017
Sponsor
Oregon Health and Science University
Collaborators
National Institute on Aging (NIA), National Center for Research Resources (NCRR)
search

1. Study Identification

Unique Protocol Identification Number
NCT00090402
Brief Title
Fish Oil and Alpha Lipoic Acid in Treating Alzheimer's Disease
Official Title
Fish Oil and Alpha Lipoic Acid in Mild Alzheimer's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
April 2004 (Actual)
Primary Completion Date
January 3, 2006 (Actual)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University
Collaborators
National Institute on Aging (NIA), National Center for Research Resources (NCRR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine the effect of fish oil and the antioxidant alpha lipoic acid on factors in the blood that are associated with the progression of Alzheimer's Disease (AD).
Detailed Description
Alzheimer's disease (AD) is a serious condition associated with increased inflammation, cholesterol, and oxidative stress (a condition involving an excess of free radicals and a decrease in antioxidant levels). Fish oil and alpha lipoic acid, which have few side effects, may help relieve these problems; therefore, these supplements may slow the progression of AD, particularly when given in combination. This study will evaluate the effect of fish oil and alpha lipoic acid on inflammation, lipid levels, and oxidative stress. Participants in this study will be randomly assigned to receive fish oil alone, fish oil and alpha lipoic acid, or placebo for 1 year. AD rating scales as well as urine and blood tests will be used to assess participants. Participants will have monthly clinic visits during the study to monitor adverse events and to undergo various laboratory tests.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease, Oxidative Stress, Dementia, Hyperlipidemia, Inflammation
Keywords
Fish Oils, Thioctic Acid, Antioxidants, Dietary Supplements

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
39 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fish Oil Placebo & Lipoic Acid Placebo
Arm Type
Placebo Comparator
Arm Description
Three 1-gram placebo-fish oil capsules (2 in the morning, 1 evening) plus one 600 milligram placebo-lipoic acid per day. Placebo fish oil capsules consisted of soybean oil flavored with lemon flavor and 5% fish oil to match fish oil capsules. LA placebo contained no LA and the following excipients: lactose, hypromellose, silicon dioxide, microcrystalline cellulose, polyethylene glycol, povidone, corn starch, talc, and magnesium stearate.
Arm Title
Fish Oil Only
Arm Type
Active Comparator
Arm Description
Three 1-gram fish oil concentrate capsules in triglyceride form (675 milligrams DHA and 975 milligrams EPA), 2 in the morning and 1 in the evening, plus one 600 milligram placebo-lipoic acid (containing no LA and the following excipients: lactose, hypromellose, silicon dioxide, microcrystalline cellulose, polyethylene glycol, povidone, corn starch, talc, and magnesium stearate) per day.
Arm Title
Fish Oil Plus Lipoic Acid
Arm Type
Experimental
Arm Description
Three 1-gram placebo-fish oil capsules (2 in the morning, 1 evening) plus one 600 milligram lipoic acid (LA) capsule in the racemic form per day.
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil
Other Intervention Name(s)
Fish oil concentrate, omega-3 fatty acids
Intervention Description
Fish oil capsule
Intervention Type
Dietary Supplement
Intervention Name(s)
Lipoic Acid
Other Intervention Name(s)
thiotic acid, alpha lipoic acid
Intervention Description
Lipoic acid capsule
Intervention Type
Other
Intervention Name(s)
Fish Oil Placebo
Other Intervention Name(s)
Placebo (for fish oil)
Intervention Description
Soybean oil placebo capsule
Intervention Type
Other
Intervention Name(s)
Lipoic Acid Placebo
Other Intervention Name(s)
Placebo (for lipoic acid)
Intervention Description
Lipoic acid (LA) placebo capsule containing no LA
Primary Outcome Measure Information:
Title
F2-isoprostane Level Urine F2-Isoprostanes
Description
F2-isoprostane is a biomarker was used as an effective indicator for detecting a decrease in systemic oxidative damage (oxidative damage in lipids). Urine F2-Isoprostanes were used to avoid ex vivo lipid peroxidation that can occur with plasma samples.
Time Frame
baseline, 12 months
Title
Change in Mini-Mental State Exam (MMSE) Score From Baseline to 12 Months
Description
The MMSE is a measure of global cognitive function, and scores range from 0-30, with a lower score indicates greater cognitive impairment.
Time Frame
baseline, 12 months
Secondary Outcome Measure Information:
Title
Change in Activities of Daily Living/Instrumental Activities of Daily Living (ADL/IADL) Scores From Baseline to 12 Months
Description
The Activities of Daily Living/Instrumental Activities of Daily Living (ADL/IADL) measures an individual's ability to carry out tasks that are important for daily living and capture functional changes. Scores for each question range from 0 (no assistance needed) to 2 (full assistance needed), and were assessed by informant interview. The combination of scores for ADL (ranging from 0-18) and IADL (0-14) is the outcome (0-32), with higher scores indicating lesser ability to carry out daily living tasks.
Time Frame
baseline, 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of probable Alzheimer's Disease or mild cognitive impairment Mini Mental State Examination (MMSE) score between 18 and 26 Clinical Dementia Rating (CDR) of 0.5 or 1.0 Fluent in English Exclusion Criteria: Use of lipid lowering medications Consumption of fish of more than twice a week Use of omega and alpha lipoic acid supplements Use of systemic corticosteroids, neuroleptics, anti-Parkinsonian agents, or narcotic analgesics Depression Any other serious health conditions that may interfere with the study Enrollment in another clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lynne H. Shinto, ND
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oregon Health and Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15339646
Citation
Calon F, Lim GP, Yang F, Morihara T, Teter B, Ubeda O, Rostaing P, Triller A, Salem N Jr, Ashe KH, Frautschy SA, Cole GM. Docosahexaenoic acid protects from dendritic pathology in an Alzheimer's disease mouse model. Neuron. 2004 Sep 2;43(5):633-45. doi: 10.1016/j.neuron.2004.08.013.
Results Reference
background
PubMed Identifier
12873849
Citation
Morris MC, Evans DA, Bienias JL, Tangney CC, Bennett DA, Wilson RS, Aggarwal N, Schneider J. Consumption of fish and n-3 fatty acids and risk of incident Alzheimer disease. Arch Neurol. 2003 Jul;60(7):940-6. doi: 10.1001/archneur.60.7.940.
Results Reference
background
PubMed Identifier
12897407
Citation
Lovell MA, Xie C, Xiong S, Markesbery WR. Protection against amyloid beta peptide and iron/hydrogen peroxide toxicity by alpha lipoic acid. J Alzheimers Dis. 2003 Jun;5(3):229-39. doi: 10.3233/jad-2003-5306.
Results Reference
background
PubMed Identifier
24077434
Citation
Shinto L, Quinn J, Montine T, Dodge HH, Woodward W, Baldauf-Wagner S, Waichunas D, Bumgarner L, Bourdette D, Silbert L, Kaye J. A randomized placebo-controlled pilot trial of omega-3 fatty acids and alpha lipoic acid in Alzheimer's disease. J Alzheimers Dis. 2014;38(1):111-20. doi: 10.3233/JAD-130722.
Results Reference
result

Learn more about this trial

Fish Oil and Alpha Lipoic Acid in Treating Alzheimer's Disease

We'll reach out to this number within 24 hrs