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The Effects of Specialty Coffee on Cognitive Function in People With Type 2 Diabetes

The Effects of CGA-rich Coffee on Cognitive Function in Type 2 Diabetes: A Parallel Groups Randomised Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05709847
Enrollment
70
Registered
2023-02-02
Start date
2023-01-01
Completion date
2025-01-01
Last updated
2023-02-02

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

Conditions

Type 2 Diabetes

Brief summary

Coffee has been found to have beneficial effects on cognitive function and blood sugar control. Benefits include reduced risk of cognitive decline and improved performance on cognitive tests, as well as reduced risk of diabetes and improved blood sugar control in people with diabetes, a population that is at a higher risk of cognitive decline. These effects have been observed for both caffeinated and decaffeinated coffee, and have been associated with the polyphenol chlorogenic acid (CGA). This polyphenol has been found to be more bioavailable in certain coffees, known as speciality coffee as defined by the Specialty Coffee Association of America, depending on agriculture, roasting, and brewing method. This current project will bring together these previous findings to explore the effects of specialty coffee on cognitive function and glycaemic control in people with type 2 diabetes through a randomized control trial with two groups: a high CGA specialty coffee group and a conventional coffee control group. Participants will be quasi-randomly assigned to one of these two groups following the completion of a 4-week run-in period during which participants will consume conventional coffee only. The length of the experimental arms is 8 weeks, therefore the total length of the study is 12 weeks. At the beginning and the end of each experimental arm participants will undertake a cognitive assessment online using the Gorilla platform, and a series of questionnaires relating to health and mood measures (details in procedure). Cognitive function will also be assessed at the beginning of the 4-week run-in period.

Interventions

OTHERCoffee

24 ounces of coffee will be consumed daily

Sponsors

University of Reading
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
55 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age 55-70 years * Formal diagnosis of Type 2 Diabetes for 3 years or more * Current coffee drinkers, 4 or fewer cups daily (a cup is 8 oz)

Exclusion criteria

* Insulin-dependent * Consuming on average more than 4 cups of coffee daily * Regularly consuming specialty coffee (participants will be provided with a list of these coffees)

Design outcomes

Primary

MeasureTime frameDescription
Verbal memory8 weeksAssessed at the end of 8-week intervention arm using a modified version of the Rey Auditory Verbal Learning Test

Secondary

MeasureTime frameDescription
Lipid panel (total cholesterol, HDL, LDL, triglycerides)8 weeksSelf-reported by the participant at the end of the 8-week intervention arm
Depression symptoms8 weeksAssessed at the end of the 8-week intervention arm with the PHQ-9
Anxiety symptoms8 weeksAssessed at the end of the 8-week intervention arm with the GAD-7
Haemoglobin A1C8 weeksSelf-reported by the participant at the end of the 8-week intervention arm
Working memory0 weeksAssessed at the beginning of the 8-week intervention arm with a computerised version of digit span
Processing Speed8 weeksAssessed at the end of the 8-week intervention arm with a computerised version of the Digit Symbol Substitution Test
Executive Function8 weeksAssessed at the end of the 8-week intervention arm with a computerised version of the Corsi Block Tapping Test

Countries

United States

Contacts

Primary ContactDaniel J Lamport, PhD
daniel.lamport@reading.ac.uk+44 (0)1183785032

Outcome results

None listed

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