Effects of Caffeine Ingestion on Morning Cognitive and 4-km Time Trial Performance in Males

March 9, 2026 updated by: spsbedwa@ljmu.ac.uk, Liverpool John Moores University

Effects of Caffeine Ingestion on Morning Cognitive and 4-km Time Trial Performance in Males. Where a Standardized Approach Has Been Employed

Athletes often compete in the morning when they are biologically weaker; normally in competition heats or quarterfinals to qualify for the finals scheduled in the evening. Some athletes may even choose to perform at submaximal levels in these qualifying rounds, especially when they are expected to perform multiple times in the same day (such as weightlifting at the Olympic Games). Gross muscular performance such as power output or force production is greater in the evening than the morning (~3-14% variation). Similarly, time-trial performance and repeated sprint performance (RSP; a good measure of performance in team sport) is ~3 and 5 % greater in the evening than the morning.

The reason for this daily variation in performance is attributed to central factors (such as the body clock), as well as motivational and peripheral factors, including higher core and muscle temperatures in the evening compared to the morning. The body clock located within the anterior hypothalamus consists of a group of neurons known as suprachiasmatic nuclei, which are responsible for controlling the rhythm of core temperature.

The most efficient nutritional ergogenic is caffeine. Recently caffeine has been investigated to reduce the negative influence of diurnal variations on repeated-sprint ability test (10 × 6 s cycle sprints, with 30 s of rest) at 60 min after ingestion of either 5 mg·kg-1 or placebo. Lopes-Silva et al. (2019) reported that caffeine supplementation did not prevent the reduction in performance in the morning. However, placebo effect can be 3-5% and hence the use of a No-pill condition would ensure that any placebo effect is accounted for and that the true potential effect of caffeine can be established.

To the best of our knowledge, no study has yet investigated caffeine (CAFF), NoPill (NOPILL) or Placebo (PLAC) effects on cognitive and 4-km time-trial (TT) performance. As a diurnal variation in 4-km TT has been widely reported in a similar population. The aim of the present study is to investigate if ingesting caffeine on the day of the morning test, to improve performance.

Study Overview

Status

Active, not recruiting

Study Type

Interventional

Enrollment (Estimated)

15

Phase

  • Phase 2
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Merseyside
      • Liverpool, Merseyside, United Kingdom, L3 3AF
        • Tom Reilly Building (LJMU)

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy adults
  • 18-35 years old
  • Injury-free
  • ≥ 2 years of weight/strength training experience
  • Not receiving any pharmacological treatment (including non-steroidal anti-inflammatory drugs, NSAIDs) throughout the study period
  • Low habitual caffeine consumers (≤ 150mg per day)
  • No preference to training regarding time-of-day

Exclusion Criteria:

  • Depressed mood (from the Beck depression inventory)
  • Poor sleep quality (a Pittsburgh sleep quality index global score >5
  • Recent shift work or travel across multiple time-zones
  • Extreme chronotype (assessed via the Composite Morningness Questionnaire
  • Risk factors and/ or symptoms of cardiovascular disease.

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1
1) NoPill, 2) PLAC, 3) Caffeine (300 mg)
No capsules were given
300mg of of caffeine anhydrous in 3 capsules similar to PLACEBO in size and weight
3 capsules of PLACEBO similar to caffeine condition in size and weight
Experimental: Group 3
1) Caffeine (300 mg) 2) NoPill, 3) PLAC
No capsules were given
300mg of of caffeine anhydrous in 3 capsules similar to PLACEBO in size and weight
3 capsules of PLACEBO similar to caffeine condition in size and weight
Experimental: Group 2
1) PLAC, 2) Caffeine (300 mg), 3) NoPill,
No capsules were given
300mg of of caffeine anhydrous in 3 capsules similar to PLACEBO in size and weight
3 capsules of PLACEBO similar to caffeine condition in size and weight

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Morning Rey Auditory Verbal Learning Test
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Rey Auditory Verbal Learning Test: The RAVLT is a neuropsychological assessment designed to evaluate verbal memory. The test is designed as a list-learning paradigm in which the volunteer hears a list of 15 nouns and is asked to recall as many words from the list as possible. The number correct and the number that were given by the participant but not on the list (intrusions) are noted. This process is re-peated 4 more times. The process is repeated but with a second interference list (List B) is presented in the same manner, and the participant is asked to recall as many words as possible from List B and scoring recorded. . After the interference trial, the participant is immediately asked to recall the words from List A, which they heard five times previously and the number of correct words and intrusions are recorded. RAVTL total number, number of dis-tractions and retention are recorded and analysed.
From familiarisation to the final experimental session (~4 weeks)
Morning Stroop word-colour interference test
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Stroop word-colour interference test. The participants were asked to read out their responses to words or colours for 45 s as quickly as possible and to leave no errors uncorrected. This was filmed and the number of errors and total amount completed was recorded and analysed. The first sheet had text (red, blue, yellow, black and green) in black ink (naming word test, W). The second sheet had blocks of colour corresponding to the text on the first sheet (naming colour test, C). With the third sheet, the participants had to read out the word (which was coloured differently to the word, e.g., the word was yellow and the colour red, referred to as the naming colour of word test, CW) and for the fourth sheet, the participants had to read out the colon (which was wrongly named, e.g., the colour was yellow but the word was red, referred to as the naming of word not colour test, WC). In this fourth sheet, the words were printed in the reverse order to the third sheet.
From familiarisation to the final experimental session (~4 weeks)
Morning Trail Making Test time to completion in seconds (TMT; parts A and B)
Time Frame: From enrolment to last experimental session (4 weeks)
To assess the effect of 300 mg caffeine (CAFF) vs placebo (PLAC) vs no-pill (NoPill) on morning Trail Making Test time to completion in seconds (TMT; parts A and B). In part A the circles are numbered 1-25, and the participant is instructed to draw lines to connect the numbers in ascending order. In part B, the circles include both numbers (1-13) and letters (A-L) and the participant is instructed to draw lines to connect the circles in ascending pattern but with the added task of alternating between numbers and letters (i.e., 1-A-2-B-3-C etc.). In both parts the participant is instructed to connect to the circles as fast as possible, without lifting the pencil from the paper. If an error is made, this is pointed out immediately and the participant is allowed to correct it. During the test, time to completion is measured, with a higher time indicative of the greater impairment.
From enrolment to last experimental session (4 weeks)
Morning 4-km time-trial finishing time
Time Frame: From enrolment to last experimental session (~4 weeks)
4-km cycling time-trial (Watbike Pro, Nottingham UK) finishing time in minute and seconds. ~ 4-6 minutes.
From enrolment to last experimental session (~4 weeks)
4-km cycling time-trial split times every 1 km.
Time Frame: From familiarisation to the final experimental session (~4 weeks)
4-km cycling time-trial (Watbike Pro, Nottingham UK) split times (in minutes and seconds) every 1 km.
From familiarisation to the final experimental session (~4 weeks)
Heart rate every 1-km
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Heart rate measured every 1-km during the 4-km time-trial, using a heart rate monitor.
From familiarisation to the final experimental session (~4 weeks)
Rating of perceived exertion every 1-km
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Rating of perceived exertion every 1-km for the 4-km time-trail. Measured on a 6 (no exertion) to 20 (maximal exertion) scale. Takes ~1 s.
From familiarisation to the final experimental session (~4 weeks)
Perceived pacing taken at 2 and 4 km
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Perceived pacing taken at 2 and 4 km of the 4-km time trial. The scale is a 10 cm visual analogue scale where -5 represents pacing to slow to complete the 2 km as fast as possible, zero = optimal pacing and +5 went to fast. Takes ~1 s to answer.
From familiarisation to the final experimental session (~4 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Morning profile of mood states questionnaire
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Morning profile of mood states questionnaire (POMS; Version 32) for moods: vigour, tension, calmness, happiness, confusion, depression and fatigue on a visual analogue scale (0=not at all and 4 = extremely). Each mood is the addition of scores for the 4 questions associated with the mood. ~ 60 s each task.
From familiarisation to the final experimental session (~4 weeks)
Sleep questions from the Liverpool Jet lag Questionnaire
Time Frame: From familiarisation to the final experimental session (~4 weeks)
Sleep questions from the Liverpool Jet lag Questionnaire: get to sleep, how well slept, waking time and alertness after waking. Measured on a -5 (later or worst) to +5 scale (more or earlier) where ZERO is compared to normal.
From familiarisation to the final experimental session (~4 weeks)
Habitual caffeine consumption
Time Frame: Baseline
Habitual caffeine consumption was assessed using the caffeine consumption questionnaire (CCQ), where caffeine intake was assessed in the morning, afternoon, evening and night. Total daily intake was expressed in mg.
Baseline
Chronotype
Time Frame: Baseline
Extreme chronotype (assessed via the Composite Morningness Questionnaire) to assess morning, intermediate and evening types. Where Evening type scores 22 and less, Intermediate type 22-43 and Morning type 44 and above.
Baseline
Self-reported 2-week training diary
Time Frame: Baseline
No preference to training regarding time-of-day by a weekly self-reported 2-week training diary for type of exercise, duration, intensity and time of day. With time of day of exercise preference recorded.
Baseline
Depressed mood
Time Frame: Baseline
Depressed mood severity from the Beck depression inventory (BDI).21 questions were answered (with 4 answers, 0= I do not feel and 3 = I am so..). The values summated to scores where 0-9 is minimal depression, 10-18 mild and 19-29 moderate depression. 30-63 sever depression. This takes 60 s to complete.
Baseline
Rectal temperature @rest and after warm-up
Time Frame: From enrolment to last experimental session (4 weeks)
Rectal temperature by a soft flexible rectal probe (mini-thermistor, Grant Instruments, Shepreth, UK) approximately 10 cm beyond the external anal sphincter. Duration in each session no longer than 35 mins.
From enrolment to last experimental session (4 weeks)
Blood lactate @ rest, pre TT and after
Time Frame: From enrolment to last experimental session (4 weeks)
Blood lactate (finger tip) values will betaken @ rest, pre TT and after
From enrolment to last experimental session (4 weeks)
Mean skin temperature (Tsk)
Time Frame: From familiarisation to the final experimental session (~4 weeks)

Mean Skin temperature (Tsk) was assessed simultaneously by skin thermistors (Grant Instruments, Squirrel 2010 series, Shepreth, UK), which were placed at four locations on the left side of the body (chest [ch], forearm [f], thigh [th] and calf [ca]). Duration in each session no longer than 35 mins.

Mean Tsk was calculated as follows:

Tsk = (0.34 x Tch) + (0.33 x Tth) + (0.18 x Tca) + (0.15 x Tf)

From familiarisation to the final experimental session (~4 weeks)
The mean body temperature (Tmb)
Time Frame: From familiarisation to the final experimental session (~4 weeks).
The mean body temperature (Tmb) was calculated using skin thermistors from 4 skin sites on the left side of the body (chest [ch], forearm [f], thigh [th] and calf [ca]). : Tmb = (0.64 x Tr) + (0.36 x Tsk)
From familiarisation to the final experimental session (~4 weeks).
7-day food diary
Time Frame: Baseline
7-day food diary that was analyzed using Nutritics® analysis software by a SENr registered Sports and Exercise Nutritionist. Data is presented in macro-nutrients and micro-nutrient diet (mg or g).
Baseline
Poor sleep quality
Time Frame: At the start of the study as part of exclusion criteria
Poor sleep quality (as indicated by the Pittsburgh sleep quality index global score >5).
At the start of the study as part of exclusion criteria
Caffeine withdrawal symptoms score
Time Frame: From familiarisation to the final experimental session (~4 weeks).
Caffeine withdrawal symptoms (total score) assesses caffeine withdrawal symptoms. Participants were asked to rate each of the 32 questions in terms of how they were feeling at that moment on a 5-pt. scale from 0 (not at all) to 4 (extremely). Eight of the items are positively worded (e.g., energetic) and were reversed scored prior to analyses. At start and during the protocol.]
From familiarisation to the final experimental session (~4 weeks).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ben J Edwards, PHD, Liverpool John Moores University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

January 12, 2026

Primary Completion (Estimated)

March 25, 2026

Study Completion (Estimated)

March 25, 2026

Study Registration Dates

First Submitted

February 25, 2026

First Submitted That Met QC Criteria

March 9, 2026

First Posted (Actual)

March 13, 2026

Study Record Updates

Last Update Posted (Actual)

March 13, 2026

Last Update Submitted That Met QC Criteria

March 9, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

IPD unavailable due to privacy or ethical restrictions

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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