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How pain affects mental fatigue, movement, and cycling performance in recreational cyclists.

Understanding the effects of pain on mental fatigue, biomechanics and performance of recreational cyclists.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000123347
Enrollment
20
Registered
2026-01-30
Start date
2026-05-01
Completion date
2026-12-28
Last updated
2026-02-09

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

Conditions

None listed

Brief summary

This study aims to explore how mental fatigue affects cycling performance and body movement in recreational cyclists, and whether these effects differ between cyclists who experience musculoskeletal pain and those who do not. Mental fatigue (caused by long periods of concentration) may make pain feel worse and reduce physical performance, but this has not been tested in cyclists. We hypothesize mentally fatigued cyclists will show lower performance, altered movement patterns, and greater discomfort, with stronger effects in those who already have pain. Understanding this relationship could support better pain-management strategies tailored to mental state. It may also help optimize training, recovery, and rehabilitation for cyclists with pain.

Interventions

Mental fatiguing task: For the mentally fatigue intervention, participants complete an electronically administered 30-minute modified Stroop test. The Stroop test requires response inhibition and sustained attention and is recognized and validated as an effective method for inducing mental fatigue. The version of the Stroop test to be used is a publicly available app-based program called “Brainiversity” (Version 2.0 for personal computer). On a tablet the Stroop test requires participants to an

Mental fatiguing task: For the mentally fatigue intervention, participants complete an electronically administered 30-minute modified Stroop test. The Stroop test requires response inhibition and sustained attention and is recognized and validated as an effective method for inducing mental fatigue. The version of the Stroop test to be used is a publicly available app-based program called “Brainiversity” (Version 2.0 for personal computer). On a tablet the Stroop test requires participants to answer multiple choice questions by selecting the colour of a word when it was different to the name of the word (e.g., selecting “blue” when the word “red” is printed in blue). There were four options to choose from per question. Participants were instructed to respond as accurately and quickly as possible to cues presented on the screen. The number of correct answers after each 60s Stroop test is recorded as the participants score for each of the 30 trials. No time restraints are imposed and upon completion of all trials, the test was reset until the 30-minute threshold had been reached. Adherence to the mental fatiguing intervention will be monitored through direct supervision and task performance metrics recorded by the Stroop test software: Participants complete the task under researcher observation to ensure continuous engagement, correct task execution, and to prevent use of external distractions (e.g., mobile phones or unrelated applications). Task completion will be verified by confirming that participants complete the full 30-minute protocol without interruption. Also, performance data generated by the application (number of correct responses per 60-second trial, for all 30 trials) will be reviewed to confirm ongoing task engagement. Consistently low or absent responses within a trial were used as indicators of non-adherence or disengagement; however, no participants will be excluded on this basis. Participants will also be verbally reminded at standardized intervals to maintain focus and respond as quickly and accurately as possible. Each participant will attend two testing sessions scheduled one week apart. One session will involve completion of the mental fatigue task, and the other will involve the control task. All participants will therefore complete both conditions. The order in which participants complete the mental fatigue and control sessions will be randomly allocated prior to testing using a coin toss. Cardiorespiratory fitness will be assessed after the completion of the mental fatiguing task and the control task in a standardised manner via a symptom-limited graded exercise test (GXT). Participants will complete the GXT on a cycle ergometer (Excalibur Sport; Lode B.V. Groningen, Netherlands) using a ramp protocol. The test will consist of stationary cycling at a cadence of 90 ±2 revolutions per minute, with a starting resistance of 100 W, until volitional exhaustion is reached. Heart rate (Polar Electro Oy, Kempele, Finland) will be monitored throughout the test with peak value recorded at cessation.

Sponsors

La Trobe University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

Recreational cyclists with no current musculoskeletal pain. Recreational cyclists with musculoskeletal pain related to cycling. Only participants who are currently cycling a minimum of 60 km per week, will be deemed eligible to participate. Participants deemed low risk after screening using the Exercise and Sports Science Australia Pre-Exercise Screening tool will be eligible for inclusion. This tool is a nationally recognised screening system designed to identify health conditions or symptoms that may increase the risk of an adverse event during physical activity.

Exclusion criteria

Risk stratification will be conducted using the compulsory part (stage 1) of the Exercise and Sports Science Australia Pre-Exercise Screening tool . Stage 1 includes questions that screen for known cardiovascular, metabolic or respiratory conditions, as well as symptoms such as unexplained chest pain, dizziness, syncope, or poorly controlled chronic disease. It also identifies individuals with musculoskeletal conditions that may be aggravated by exercise. Participants deemed medium to high risk after screening using the Exercise and Sports Science Australia Pre-Exercise Screening tool will be excluded. Participants to be excluded if they have any known mental or physical disorders, including history of neurological conditions, beyond items from the Pre-Exercise Screening tool. Participants to be excluded below 18 years of age and above 64 years because of maturation stage and changes in musculoskeletal fitness from ageing, respectively.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 15, 2026