Cataract and AMD in a Trial of a Multivitamin and Cocoa Extract

NCT ID: NCT03205202

Last Updated: 2021-09-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

21442 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-06-01

Study Completion Date

2022-10-31

Brief Summary

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COSMOS-Eye is an ancillary study of the COcoa-Supplement and Multivitamins Outcomes Study (COSMOS; NCT02422745). COSMOS is a randomized clinical trial of cocoa extract supplement (containing a total of 500 mg/d flavanols, including 80 mg (-)-epicatechins), and 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 is being conducted among participants in COSMOS and will examine whether the cocoa extract supplement or the multivitamin supplement reduces the risk of cataract and AMD, two leading causes of visual impairment in US men and women.

Detailed Description

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COSMOS-Eye is an ancillary study of cataract and AMD utilizing resources and data from the COcoa-Supplement and Multivitamins Outcomes Study (COSMOS), a randomized, double-blind, placebo-controlled, 2x2 factorial trial of a high-quality cocoa extract supplement (Mars Symbioscience) and Centrum Silver multivitamin (Pfizer) in the prevention of cardiovascular disease and cancer among 12,000 women aged ≥65 years and 6,000 men aged ≥60 years.

Women will be recruited among active Women's Health Initiative (WHI) Extension Study participants, and men will be recruited among non-randomized respondents to the VITamin D and OmegA-3 Trial (VITAL). Women who responded but were not randomized into VITAL will also be included as well as other women and men who express interest in research being conducted at Brigham and Women's Hospital.

Participants will take three pills each day: two capsules that contain either cocoa extract or cocoa extract placebo, and one tablet that contains either multivitamin or multivitamin placebo. Participants will receive their study pills in convenient calendar packs via U.S. mail.

Participants also will be asked to complete short mailed questionnaires each year. The questionnaires ask about health; lifestyle habits, such as diet, physical activity, and smoking; use of medications and dietary supplements; family history of illness and new medical diagnoses including cataract and AMD.

Participants who report cataract or AMD will be asked to provide contact information for their eye doctor(s) as well as written consent to obtain the medical records. Eye doctors will be contacted by mail and asked to complete a cataract (or AMD) questionnaire or, alternatively, forward a complete copy of the patient's medical records pertaining to the diagnosis.

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.

Conditions

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Cataract Age Related Macular Degeneration

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Cocoa extract + multivitamin

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

Dietary Supplement: Multivitamin

Group Type ACTIVE_COMPARATOR

Cocoa extract

Intervention Type DIETARY_SUPPLEMENT

Multivitamin

Intervention Type DIETARY_SUPPLEMENT

Cocoa extract + multivitamin placebo

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

Dietary Supplement: Multivitamin placebo

Group Type ACTIVE_COMPARATOR

Cocoa extract

Intervention Type DIETARY_SUPPLEMENT

Multivitamin placebo

Intervention Type DIETARY_SUPPLEMENT

Cocoa extract placebo + multivitamin

Dietary Supplement: Multivitamin

Dietary Supplement: Cocoa extract placebo

Group Type ACTIVE_COMPARATOR

Multivitamin

Intervention Type DIETARY_SUPPLEMENT

Cocoa extract placebo

Intervention Type DIETARY_SUPPLEMENT

Cocoa extract placebo + multivitamin placebo

Dietary Supplement: Cocoa extract placebo

Dietary Supplement: Multivitamin placebo

Group Type PLACEBO_COMPARATOR

Cocoa extract placebo

Intervention Type DIETARY_SUPPLEMENT

Multivitamin placebo

Intervention Type DIETARY_SUPPLEMENT

Interventions

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Cocoa extract

Intervention Type DIETARY_SUPPLEMENT

Multivitamin

Intervention Type DIETARY_SUPPLEMENT

Cocoa extract placebo

Intervention Type DIETARY_SUPPLEMENT

Multivitamin placebo

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

Participants in COSMOS who 1) report a diagnosis of cataract or AMD, or extraction of cataract, and 2) provide written consent to obtain the medical records for the reported endpoint, are eligible for this ancillary study.
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Brigham and Women's Hospital

OTHER

Sponsor Role lead

Responsible Party

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William G. Christen

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

References

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Christen WG, Rist PM, Moorthy MV, Smith DC, Holman B, Clar A, Glynn RJ, Mares JA, Sobrin L, Shadyab AH, Allison MA, Millen AE, Manson JE, Sesso HD; COSMOS Research Group. Cocoa Flavanol Supplementation and Risk of Age-Related Macular Degeneration: An Ancillary Study of the COSMOS Randomized Clinical Trial. JAMA Ophthalmol. 2025 May 1;143(5):429-437. doi: 10.1001/jamaophthalmol.2025.0353.

Reference Type DERIVED
PMID: 40146119 (View on PubMed)

Other Identifiers

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2016P001612

Identifier Type: -

Identifier Source: org_study_id

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