NCT07130825 The Effect of Different Physical Activity Strategy on Cognitive Efficiency and Mental Fatigue Resistance
| NCT ID | NCT07130825 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Lithuanian Sports University |
| Condition | Healthy Adults |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-08-01 |
| Primary Completion | 2031-03-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2025-08-01 with a primary completion date of 2031-03-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The main aim of this biomedical study is to determine the effect of moderate-intensity aerobic exercise, before and after an 8-hour workday and a combined work model, on the performance and efficiency of cognitive functions during mental work. There are lack of previous studies analysing the effects of different physical activity strategies on cognitive efficiency and investigating mental fatigue resistance. Limited research in this area shows that the mechanism of the effect of physical activity on mental fatigue resistance is still unclear. This research will aim to investigate different physical activity strategies, such as combined work model and moderate intensity physical activity before and after office workday, and their impact on a mental and emotional fatigue, cognitive efficiency, sympathetic and parasympathetic systems and metabolic indicators during mentally demanding 8 h workday.
Eligibility Criteria
Inclusion Criteria: * BMI from 18.5 to 24.9 kg/ m2; * No chronic non-communicable diseases; * No mental illnesses or disorders; * No cancer and no chemotherapy in the last 5 years; * No hearing impairment; * No smoking; * No psychotropic substances; * Heart rate (HR) about 60 bpm at rest; * Unimpaired color vision; * Unimpaired or corrected vision; * Systolic blood pressure from 90 to 139 mmHg, and diastolic - from 50 to 89 mmHg at rest. Exclusion Criteria: * mental, oncological, metabolic, cardiovascular, skeletal, muscular, respiratory system disorders or diseases, impaired color vision.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07130825 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Healthy Adults. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07130825 currently recruiting?
Yes, NCT07130825 is actively recruiting participants. Contact the research team at marius.brazaitis@lsu.lt for enrollment information.
Where is the NCT07130825 trial being conducted?
This trial is being conducted at Kaunas, Lithuania.
Who is sponsoring the NCT07130825 clinical trial?
NCT07130825 is sponsored by Lithuanian Sports University. The trial plans to enroll 60 participants.