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Immune Benefits of Coffee

Effect of Coffee Consumption on Immune and Inflammatory Status in Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00860197
Enrollment
116
Registered
2009-03-12
Start date
2009-03-31
Completion date
2010-02-28
Last updated
2015-12-02

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

Conditions

Immune Senescence, Low-grade Inflammation

Keywords

Coffee, Elderly, Immune response, Inflammatory status

Brief summary

This study will assess whether coffee consumption: * increases immune responses * decreases inflammatory status

Detailed description

Epidemiological studies suggest that coffee consumption is associated with protective effects against several types of chronic diseases. Recent data have shown that certain coffee components may possess anti-inflammatory and immune-enhancing properties. Low-grade inflammation and poor capacity of immune response is highly prevalent in elderly subjects. The purpose of this study is to evaluate whether coffee consumption improves immune and inflammatory status in healthy elderly subjects. To sort out the role of antioxidants, we will test 2 different soluble coffee, i.e. fully torrefied coffee and partially torrefied coffee.

Interventions

DIETARY_SUPPLEMENTFully torrefied coffee

Fully torrefied coffee

DIETARY_SUPPLEMENTPartially torrefied coffee

Partially torrefied coffee

Sponsors

Société des Produits Nestlé (SPN)
CollaboratorINDUSTRY
University of Chile
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy, self-sufficient, free-living Chilean elderly * Having the ability to comprehend the procedures of the study * Having obtained his/her informed consent after verbal and written information

Exclusion criteria

* Subjects drinking more than 2 cups of coffee per day * Subjects with rapidly deteriorating health status at enrolment in the study * Subjects with terminal or acute disease, or unstable health status * Subjects with chronic disease: chronic respiratory illness; chronic diseases of the pulmonary or cardiovascular systems (including asthma); chronic metabolic disease (diabetes); chronic renal disease, organ failure * Subjects with serious neurological disorder, including dementia (MMSE \< 20) or Alzheimer's disease * Subjects who have experienced rapid weight loss, chronic diarrhea (loose stools, 3 times daily), or Crohn's (IBD) * Subjects with gastrointestinal problems * Subjects with a hospitalization planned during this study * Subjects who have received any antibiotic treatment during the last 3 months prior to the beginning of this study * Subjects who had a colonoscopy performed during the last 3 months prior to the beginning of this study * Subjects with immune deficiency diseases (e.g. HIV infection) * Subjects with a history of allergy - especially to egg protein, egg, shellfish or the antibiotics polymyxin or neomycin * Subjects receiving medication that may influence the immune system (i.e. corticosteroids, immuno-suppressors and immuno-modulators, antimicrobials) * Subjects who have received any vaccination during the last 15 days prior to baseline * Subjects who are expected to be non-compliant * Subjects currently participating or having participated in another clinical trial during the last 3 months prior to the beginning of this study * Subjects participating in another research study involving any type of medication related to the study

Design outcomes

Primary

MeasureTime frame
NK-cell activitywill be measured before and after 30 days +/- treatment
Tuberculin testwill be measured before and after 30 days +/- treatment
Inflammatory statuswill be measured before and after 30 days +/- treatment

Secondary

MeasureTime frame
Gut microbiota profilingwill be measured before and after 30 days +/- treatment

Countries

Chile

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026