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Investigating the Effects of Cocoa Flavanol on Cognition Assessed Online

COSMOS Web: Investigating the Effects of Cocoa Flavanol on Cognition Assessed Online

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04582617
Acronym
COSMOS-Web
Enrollment
3959
Registered
2020-10-09
Start date
2016-08-26
Completion date
2020-12-31
Last updated
2023-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Cognitive Change

Keywords

Cognitive Function, Cognitive Change, Aging, ModRey, Cocoa Extract, Multivitamin, Hippocampus, Executive Function, Verbal Memory, Spatial Memory

Brief summary

The COcoa Supplement and Multivitamin Outcomes Study (COSMOS; NCT02422745) is a randomized clinical trial of cocoa extract supplement (containing a total of 500 mg/d flavanols, including 80 mg (-)-epicatechin), and/or a standard multivitamin supplement to reduce the risk of cardiovascular disease and cancer among men aged 60 years and older and women aged 65 years and older. This ancillary study (COSMOS Web) is being conducted among a subset of participants in COSMOS and will examine whether the cocoa extract supplements affects cognitive function in older adults.

Detailed description

The goal of the COSMOS Web study is to determine whether a dietary intervention with flavanol-containing cocoa extract has an effect on cognitive function in older adults (age 60+). The study will be conducted in a subset of 4000 participants from the COSMOS study (NCT02422745). The investigators' recent work (Sloan et al., submitted) showed that cocoa flavanol consumption over 12 weeks led to improvements in immediate recall on the ModRey verbal memory task in healthy older adults. In COSMOS Web, the investigators are testing the effect of a dietary intervention with flavanol-containing cocoa extract on a range of aging-related cognitive measures, as assessed through a novel online-administered test battery, in a cohort of older participants. Change in ModRey (Modified Rey Auditory Verbal Learning Test) immediate recall performance over 1 year of cocoa extract consumption will be our primary outcome measure. Secondary endpoints will include change in ModRey performance at 2- and 3-year follow-up, and change in performance tests of a novel object recognition task, executive function/working memory, and spatial memory at 1-, 2-, and 3- years follow-up. This study will explore whether baseline measures of cognition and nutritional status can predict differential effects of the cocoa extract supplementation. This study will also explore the effect of multivitamin intake on the primary and secondary outcomes noted above and test whether multivitamin intake interacts with flavanol intake from cocoa extract to enhance or mitigate effects on cognitive outcomes. In a subset of participants evaluated in person, this study will examine the impact of cocoa extract intake and explore the main and interacting effects of multivitamins on cognitive changes and brain structure and function appreciated with magnetic resonance imaging over a 2-year period. Leveraging the COSMOS study, which has randomized 21,442 older adult participants into cocoa extract and placebo interventions, the study team at Brigham and Women's Hospital, who administer the parent COSMOS trial, are recruiting \ 4000 older adult volunteers to participate in COSMOS Web (this study) an online cognitive testing battery developed by the team at Columbia University. These 4000 participants will complete an initial online cognitive assessment and additional assessments after one, two, and three years of follow-up. In addition, approximately 200 COSMOS Web participants who live in the Boston area will complete clinic-based study visits at the Clinical and Translational Science Center at Brigham and Women's Hospital. During that visit, they will complete a neuropsychological test battery, for comparison to their performance online. This study will examine the impact of dietary interventions with cocoa extract and explore the main and interacting effects of multivitamin intake on cognitive changes and brain structure and function appreciated with magnetic resonance imaging over a 2-year period. After the COSMOS trial began, an advanced method to analyze cocoa flavanols was accredited by AOAC International as a First Action Official Method of Analysis (https://doi.org/10.1093/jaoacint/qsaa132). This updated method relies on a reference material (RM8403) recently standardized and made commercially available by the U.S. National Institute of Standards and Technology. While the actual cocoa flavanol content of the COSMOS intervention remained unchanged throughout the trial, the application of this new analytical method led to expected changes in how the total cocoa flavanol content is now reported. Applying AOAC 2020.05/RM8403 to the COSMOS intervention, the total cocoa flavanol content of the COSMOS intervention is now 500 mg/day. Reporting of (-)-epicatechin content remained unaffected. Going forward, we will therefore apply AOAC 2020.05/RM8403 and report that the COSMOS intervention tested 500 mg/day of cocoa flavanols, including 80 mg of (-)-epicatechin.

Interventions

DIETARY_SUPPLEMENTCocoa Extract

2 capsules each day containing a total of 500 mg cocoa flavanols, including 80 mg (-)-epicatechin, and 50 mg theobromine

DIETARY_SUPPLEMENTCocoa Extract Placebo

Cocoa extract placebo

DIETARY_SUPPLEMENTMultivitamin

Multivitamin

DIETARY_SUPPLEMENTMultivitamin placebo

Multivitamin placebo

Sponsors

Brigham and Women's Hospital
CollaboratorOTHER
Fred Hutchinson Cancer Center
CollaboratorOTHER
Mars, Inc.
CollaboratorINDUSTRY
Columbia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants in COSMOS (NCT02422745) who meet the following criteria are eligible to participate in this ancillary study: Inclusion Criteria: * Willingness to participate * Email and internet access via computer

Exclusion criteria

\* Analog to COSMOS parent trial

Design outcomes

Primary

MeasureTime frameDescription
ModRey: 1-Year Change in Immediate Recall/Learning/Episodic Memory1-year follow-upA measure of verbal memory. The change in the number of words recalled immediately on the ModRey task (Hale et al., 2019), after one year of cocoa extract/placebo intervention.

Secondary

MeasureTime frameDescription
ModBent1-year, 2-year and 3-year follow-upsA measure of pattern separation/object recognition. Change in the mean response time on correct rejection trials on a delayed recognition task.
Flanker: Directional Flanker Effect1-year, 2-year and 3-year follow-upsA measure of executive control. Change in the difference in reaction time (in ms) between directionally congruent and directional incongruent trials in a Flanker task.
Spatial Reconstruction: Distortion1-year, 2-year and 3-year follow-upsA measure of spatial memory. Change in the proportion of stimulus pairs where their relative locations are reconstructed differently than originally shown
Self-Reported Memory Change1-year, 2-year and 3-year follow-upsSelf-report of memory change in the last year, on a scale of 1-7
In-clinic ModBent2-year follow-upChange in performance on the ModBent task, administered in-clinic to a subset of 200 participants
ModRey: Longitudinal Change in Immediate Recall/Learning2-year and 3-year follow-upsA measure of verbal memory. Change in number of words recalled immediately on the ModRey task.
Hippocampal volume change2-year follow-upChange in hippocampus volume (in cubic mm) in subset of participants with in-clinic MRI scan
Global cortical thickness change2-year follow-upChange in average cortical thickness in the whole brain (in mm) in subset of participants with in-clinic MRI scan
Hippocampal cerebral blood volume change2-year follow-upChange in cerebral blood volume in the hippocampus (in cubic mm) in subset of participants with in-clinic MRI scan
Proportions of words recalled on in-clinic list learning task2-year follow-upProportions of words recalled on list learning task for subset of participants with in-clinic cognitive testing
Interaction of Baseline Diet & Intervention on the ModRey1-year, 2-year and 3-year follow-upsInteraction of baseline diet (as assessed by the Food Frequency Questionnaire) with the flavanol/multivitamin interventions on the ModRey, a measure of verbal memory (change in number of words recalled)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026