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OpenTrials
Completed

NCT Number: NCT05245188

Evaluation of Cognitive Performance in 4 Dairy Beverages

The objective of the study is to evaluate the cognitive performance of 4 chocolate milk drinks.

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Key information

Age range

20 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Catholic University of Murcia

Murcia, 30107, Spain

About this study

Subjects will make a total of 4 visits. Four visits in which they will drink a chocolate milkshake at each visit.

At each visit the subjects will have to come fasting, and they will have to perform the cognitive test at the time when they have their peak glycemic level.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects of both sexes (10 men and 10 women).
  • Subjects aged between 20 and 35 years.
  • Subjects with a body mass index between 20 and 25 kg/m2.

Exclusion criteria

  • Subjects suffering from diabetes mellitus or any chronic disease.
  • Subjects with medical problems or a diagnosed psychiatric disorder.
  • Subjects with alcohol abuse or excessive alcohol consumption (>3 glasses of wine or beer/day).
  • Subjects consuming any pharmacological medication that may affect memory.
  • Participation in another clinical trial in the three months prior to the study.
  • Unwillingness or inability to comply with clinical trial procedures.
  • Subjects whose condition does not make them eligible for the study according to the investigator's criteria.
  • Pregnant or lactating women.

Treatment and study plan

Chocolate milk shakes - Product 1

Other

11.3 glucose

Chocolate milk shakes - Product 2

Other

8.84 glucose

Chocolate milk shakes - Product 3

Other

4.24 glucose

Chocolate milk shakes - Product 4

Other

4.36 glucose

Primary outcomes

  1. Cognitive performance

    Time frame: The test was carried out half an hour after consumption of the product, except for product 4, which was carried out 15 minutes after consumption.

    COMPASS cognitive test panel

Secondary outcomes

  1. Depression, Anxiety and Stress

    Time frame: The test was carried out half an hour after consumption of the product, except for product 4, which was carried out 15 minutes after consumption.

    DASS21 test

  2. Sleep quality

    Time frame: The test was carried out half an hour after consumption of the product, except for product 4, which was carried out 15 minutes after consumption.

    Pittsburgh test

Sponsors and collaborators

Lead sponsor

Universidad Católica San Antonio de Murcia

Other

Registry information

Acronym: COG

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Feb 17, 2022
Registry last updated
Jun 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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