- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02647567
Caffeine Intake and Additive Effects on Cognition (Caffeine)
January 4, 2016 updated by: Alberto Souza de Sá Filho, Universidade Federal do Rio de Janeiro
Can Caffeine Intake Combined With Aerobic Exercise Leads to Cognitive Improvement and Psychomotor Performance in Trained Individuals?
Caffeine is a methylxanthine commonly consumed by the population for their psychostimulant properties, and their intake when in moderate doses seem to produce positive effects on stress, mood and memory.
So, understanding that a positive effect of aerobic exercise can be displayed also on cognition, as caffeine, when in proper proportions, the investigators do not know if the joining of the two strategies into a single activity would be able to promote additional effects enhancing cognitive processes related to memory, attention, and motor reaction time.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Determine if 500 mg of caffeine can generate additional effects to 30 minutes of aerobic exercise enhancing cognitive memory tasks (Rey Auditory Verbal Learning Test - RAVLT), attention (sustained attention span; working speed; Percentual of errors by confusion) and simple reaction time (SRT).
Study Type
Interventional
Enrollment (Actual)
20
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Fighting men
- Low levels of consumption of caffeine daily
Exclusion Criteria:
- Use more than 400 mg caffeine day
- Mental diseases
- Cognitive deficits
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Caffeine Intake
The experimental group ingest 500 mg of caffeine before (60 min) aerobic exercise (procedure double blind), and perform a battery of neuropsychological and psychomotor tests. 1 min and 30 min after the exercise the subjects perform a new battery of neuropsychological and psychomotor tests.
|
The experimental group ingest 500 mg of caffeine before (60 min) aerobic exercise (procedure double blind), and perform a battery of neuropsychological and psychomotor tests. 1 min and 30 min after the exercise the subjects perform a new battery of neuropsychological and psychomotor tests.
Other Names:
|
PLACEBO_COMPARATOR: Placebo Intake
The control group ingest 500 mg of placebo before (60 min) aerobic exercise (procedure double blind), and perform a battery of neuropsychological and psychomotor tests. 1 min and 30 min after the exercise the subjects perform a new battery of neuropsychological and psychomotor tests.
|
The control group ingest 500 mg of placebo before (60 min) aerobic exercise (procedure double blind), and perform a battery of neuropsychological and psychomotor tests. 1 min and 30 min after the exercise the subjects perform a new battery of neuropsychological and psychomotor tests.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Simple Reaction Time
Time Frame: Acute Change from Baseline Psychomotor test to 1 min after aerobic exercise, and after 30 min
|
Acute Change from Baseline Psychomotor test to 1 min after aerobic exercise, and after 30 min
|
Rey Auditory Verbal Learning Test
Time Frame: Acute Change from Baseline Cognitive test to 1 min after aerobic exercise, and after 30 min
|
Acute Change from Baseline Cognitive test to 1 min after aerobic exercise, and after 30 min
|
Sustained Attention Test
Time Frame: Acute Change from Baseline Cognitive test to 1 min after aerobic exercise, and after 30 min
|
Acute Change from Baseline Cognitive test to 1 min after aerobic exercise, and after 30 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2015
Primary Completion (ACTUAL)
November 1, 2015
Study Completion (ACTUAL)
December 1, 2015
Study Registration Dates
First Submitted
December 5, 2015
First Submitted That Met QC Criteria
January 4, 2016
First Posted (ESTIMATE)
January 6, 2016
Study Record Updates
Last Update Posted (ESTIMATE)
January 6, 2016
Last Update Submitted That Met QC Criteria
January 4, 2016
Last Verified
January 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UNIVERSO-03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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