Acute Effects of High-Velocity Interval Cycling Versus Continuous Moderate-Intensity Cycling on Cognitive Function in Patients with Mild Cognitive Impairment
Highlights
- A single session of high-velocity, low-resistance interval cycling acutely improved global cognition, executive functions, and semantic fluency in patients with mild cognitive impairment (MCI).
- Both high-velocity interval cycling and continuous aerobic cycling elicited cognitive benefits, whereas effects on processing speed and psychomotor vigilance were limited.
- Acute aerobic exercise may serve as a feasible non-pharmacological strategy to transiently enhance cognitive performance in MCI.
- High-velocity interval cycling induced comparable cognitive benefits with lower cardiovascular load and perceived exertion.
Abstract
1. Introduction
2. Materials and Methods
2.1. Participants
2.2. Study Design
2.3. Cognitive Assessments
2.4. Functional Tests
3. Statistical Analysis
4. Results
4.1. Acute Post-Exercise Responses and Cognitive Function (MoCA)
4.2. Acute Post-Exercise Responses and Executive Function (FAB)
4.3. Semantic Fluency (Temporal–Frontal Lexical Retrieval)
4.4. TMT-A and TMT-B (Processing Speed)
4.5. Psychomotor Vigilance Test (PVT)
4.6. Order Effect of Cognitive Data
4.7. Functional Performance
4.8. Order Effect of Functional Data
4.9. Heart Rate (HR) and Rate of Perceived Exertion (RPE) Responses
5. Discussion
5.1. Global Cognition and Executive Function
5.2. Processing Speed and Vigilance
5.3. Functional Performance
5.4. Physiological Considerations
5.5. Limitations
6. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- World Health Organization. World Report on Aging and Health. 2015. Available online: https://apps.who.int/iris/handle/10665/186463 (accessed on 1 February 2022).
- Langa, K.M.; Levine, D.A. The Diagnosis and Management of Mild Cognitive Impairment. JAMA 2014, 312, 2551. [Google Scholar] [CrossRef]
- Bennett, H.C.; Zhang, Q.; Wu, Y.T.; Manjila, S.B.; Chon, U.; Shin, D.; Vanselow, D.J.; Pi, H.-J.; Drew, P.J.; Kim, Y. Aging drives cerebrovascular network remodeling and functional changes in the mouse brain. Nat. Commun. 2024, 15, 6398. [Google Scholar] [CrossRef]
- Lee, J.; Kim, H.J. Normal Aging Induces Changes in the Brain and Neurodegeneration Progress: Review of the Structural, Biochemical, Metabolic, Cellular, and Molecular Changes. Front. Aging Neurosci. 2022, 14, 931536. [Google Scholar] [CrossRef] [PubMed]
- Olivo, G.; Nilsson, J.; Garzón, B.; Lebedev, A.; Wåhlin, A.; Tarassova, O.; Ekblom, M.; Lövdén, M. Immediate effects of a single session of physical exercise on cognition and cerebral blood flow: A randomized controlled study of older adults. Neuroimage 2021, 225, 117500. [Google Scholar] [CrossRef]
- Boa Sorte Silva, N.C.; Barha, C.K.; Erickson, K.I.; Kramer, A.F.; Liu-Ambrose, T. Physical exercise, cognition, and brain health in aging. Trends Neurosci. 2024, 47, 402–417. [Google Scholar] [CrossRef] [PubMed]
- Saucedo Marquez, C.M.; Vanaudenaerde, B.; Troosters, T.; Wenderoth, N. High-intensity interval training evokes larger serum BDNF levels compared with intense continuous exercise. J. Appl. Physiol. 2015, 119, 1363–1373. [Google Scholar] [CrossRef]
- Yu, Y.; Wang, J.; Xu, J. Optimal dose and type of exercise to improve cognitive function in patients with mild cognitive impairment: A systematic review and network meta-analysis of RCTs. Front. Psychiatry 2024, 15, 1436499. [Google Scholar] [CrossRef] [PubMed]
- Petersen, R.C.; Caracciolo, B.; Brayne, C.; Gauthier, S.; Jelic, V.; Fratiglioni, L. Mild cognitive impairment: A concept in evolution. J. Intern. Med. 2014, 275, 214–228. [Google Scholar] [CrossRef]
- Albert, M.S.; DeKosky, S.T.; Dickson, D.; Dubois, B.; Feldman, H.H.; Fox, N.C.; Gamst, A.; Holtzman, D.M.; Jagust, W.J.; Petersen, R.C.; et al. The diagnosis of mild cognitive impairment due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimer’s Dement. 2011, 7, 270–279. [Google Scholar] [CrossRef]
- Liss, J.L.; Seleri Assunção, S.; Cummings, J.; Atri, A.; Geldmacher, D.S.; Candela, S.F.; Devanand, D.P.; Fillit, H.M.; Susman, J.; Mintzer, J.; et al. Practical recommendations for timely, accurate diagnosis of symptomatic Alzheimer’s disease (MCI and dementia) in primary care: A review and synthesis. J. Intern. Med. 2021, 290, 310–334. [Google Scholar] [CrossRef]
- Livingston, G.; Huntley, J.; Liu, K.Y.; Costafreda, S.G.; Selbæk, G.; Alladi, S.; Ames, D.; Banerjee, S.; Burns, A.; Brayne, C.; et al. Dementia prevention, intervention, and care: 2024 report of the Lancet standing Commission. Lancet 2024, 404, 572–628. [Google Scholar] [CrossRef]
- Petersen, R.C.; Morris, J.C. Mild Cognitive Impairment as a Clinical Entity and Treatment Target. Arch. Neurol. 2005, 62, 1160. [Google Scholar] [CrossRef]
- Gavelin, H.M.; Dong, C.; Minkov, R.; Bahar-Fuchs, A.; A Ellis, K.; Lautenschlager, N.T.; Mellow, M.L.; Wade, A.T.; E Smith, A.; Finke, C.; et al. Combined physical and cognitive training for older adults with and without cognitive impairment: A systematic review and network meta-analysis of randomized controlled trials. Ageing Res. Rev. 2021, 66, 101232. [Google Scholar] [CrossRef]
- Meng, Q.; Yin, H.; Wang, S.; Shang, B.; Meng, X.; Yan, M.; Li, G.; Chu, J.; Chen, L. The effect of combined cognitive intervention and physical exercise on cognitive function in older adults with mild cognitive impairment: A meta-analysis of randomized controlled trials. Aging Clin. Exp. Res. 2022, 34, 261–276. [Google Scholar] [CrossRef] [PubMed]
- Huang, X.; Zhao, X.; Li, B.; Cai, Y.; Zhang, S.; Wan, Q.; Yu, F. Comparative efficacy of various exercise interventions on cognitive function in patients with mild cognitive impairment or dementia: A systematic review and network meta-analysis. J. Sport Health Sci. 2022, 11, 212–223. [Google Scholar] [CrossRef]
- Huang, X.; Li, B.; Yu, F.; Zhou, J.; Wan, Q.; Chang, H. Path analysis from physical activity to quality of life among dementia patients: A dual-path mediating model. J. Adv. Nurs. 2020, 76, 546–554. [Google Scholar] [CrossRef]
- da Langoni, C.S.; de Resende, T.L.; Barcellos, A.B.; Cecchele, B.; Knob, M.S.; Silva, T.D.N.; da Rosa, J.N.; Diogo, T.d.S.; Filho, I.G.d.S.; Schwanke, C.H.A. Effect of Exercise on Cognition, Conditioning, Muscle Endurance, and Balance in Older Adults with Mild Cognitive Impairment: A Randomized Controlled Trial. J. Geriatr. Phys. Ther. 2019, 42, E15–E22. [Google Scholar] [CrossRef]
- Leyland, L.-A.; Spencer, B.; Beale, N.; Jones, T.; van Reekum, C.M. The effect of cycling on cognitive function and well-being in older adults. PLoS ONE 2019, 14, e0211779. [Google Scholar] [CrossRef] [PubMed]
- Baker, L.D.; Frank, L.L.; Foster-Schubert, K.; Green, P.S.; Wilkinson, C.W.; McTiernan, A.; Cholerton, B.A.; Plymate, S.R.; Fishel, M.A.; Watson, G.S.; et al. Aerobic Exercise Improves Cognition for Older Adults with Glucose Intolerance, A Risk Factor for Alzheimer’s Disease. J. Alzheimer’s Dis. 2010, 22, 569–579. [Google Scholar] [CrossRef] [PubMed]
- Uygur, M.; Bellumori, M.; LeNoir, K.; Poole, K.; Pretzer-Aboff, I.; Knight, C.A. Immediate effects of high-speed cycling intervals on bradykinesia in Parkinson’s disease. Physiother. Theory Pract. 2015, 31, 77–82. [Google Scholar] [CrossRef]
- Oberlin, L.E.; Waiwood, A.M.; Cumming, T.B.; Marsland, A.L.; Bernhardt, J.; Erickson, K.I. Effects of Physical Activity on Poststroke Cognitive Function. Stroke 2017, 48, 3093–3100. [Google Scholar] [CrossRef] [PubMed]
- Fisher, B.E.; Wu, A.D.; Salem, G.J.; Song, J.; Lin, C.-H.; Yip, J.; Cen, S.; Gordon, J.; Jakowec, M.; Petzinger, G. The effect of exercise training in improving motor performance and corticomotor excitability in people with early Parkinson’s disease. Arch. Phys. Med. Rehabil. 2008, 89, 1221–1229. [Google Scholar] [CrossRef]
- Ridgel, A.L.; Phillips, R.S.; Walter, B.L.; Discenzo, F.M.; Loparo, K.A. Dynamic High-Cadence Cycling Improves Motor Symptoms in Parkinson’s Disease. Front. Neurol. 2015, 6, 194. [Google Scholar] [CrossRef]
- Tsai, C.-L.; Pan, C.-Y.; Tseng, Y.-T.; Chen, F.-C.; Chang, Y.-C.; Wang, T.-C. Acute effects of high-intensity interval training and moderate-intensity continuous exercise on BDNF and irisin levels and neurocognitive performance in late middle-aged and older adults. Behav. Brain Res. 2021, 413, 113472. [Google Scholar] [CrossRef] [PubMed]
- Ribeiro, P.A.B.; Boidin, M.; Juneau, M.; Nigam, A.; Gayda, M. High-intensity interval training in patients with coronary heart disease: Prescription models and perspectives. Ann. Phys. Rehabil. Med. 2017, 60, 50–57. [Google Scholar] [CrossRef]
- Vogiatzis, I.; Nanas, S.; Roussos, C. Interval training as an alternative modality to continuous exercise in patients with COPD. Eur. Respir. J. 2002, 20, 12–19. [Google Scholar] [CrossRef]
- Morris, J.C. The Clinical Dementia Rating (CDR): Current version and scoring rules. Neurology 1993, 43, 2412–2414. [Google Scholar] [CrossRef]
- McKhann, G.M.; Knopman, D.S.; Chertkow, H.; Hyman, B.T.; Jack, C.R., Jr.; Kawas, C.H.; Klunk, W.E.; Koroshetz, W.J.; Manly, J.J.; Mayeux, R.; et al. The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimer’s Dement. 2011, 7, 263–269. [Google Scholar] [CrossRef]
- Nasreddine, Z.S.; Phillips, N.A.; Bédirian, V.; Charbonneau, S.; Whitehead, V.; Collin, I.; Cummings, J.L.; Chertkow, H. The Montreal Cognitive Assessment, MoCA: A brief screening tool for mild cognitive impairment. J. Am. Geriatr. Soc. 2005, 53, 695–699. [Google Scholar] [CrossRef]
- Slachevsky, A.; Villalpando, J.M.; Sarazin, M.; Hahn-Barma, V.; Pillon, B.; Dubois, B. Frontal assessment battery and differential diagnosis of frontotemporal dementia and Alzheimer disease. Arch. Neurol. 2004, 61, 1104–1107. [Google Scholar] [CrossRef] [PubMed]
- Kosmidis, M.H.; Vlahou, C.H.; Panagiotaki, P.; Kiosseoglou, G. The verbal fluency task in the Greek population: Normative data, and clustering and switching strategies. J. Int. Neuropsychol. Soc. 2004, 10, 164–172. [Google Scholar] [CrossRef]
- Zalonis, I.; Kararizou, E.; Triantafyllou, N.I.; Kapaki, E.; Papageorgiou, S.; Sgouropoulos, P.; Vassilopoulos, D. A normative study of the trail making test A and B in Greek adults. Clin. Neuropsychol. 2008, 22, 842–850. [Google Scholar] [CrossRef]
- Dinges, D.F.; Powell, J.W. Microcomputer analyses of performance on a portable, simple visual RT task during sustained operations. Behav. Res. Methods Instrum. Comput. 1985, 17, 652–655. [Google Scholar] [CrossRef]
- Alencar, M.A.; Dias, J.M.D.; Figueiredo, L.C.; Dias, R.C. Handgrip strength in elderly with dementia: Study of reliability Força de preensão palmar em idosos com demência: Estudo da confiabilidade. Rev. Bras. Fisioter. 2012, 16, 510–514. [Google Scholar] [CrossRef]
- Jones, C.J.; Rikli, R.E.; Beam, W.C. A 30-s chair-stand test as a measure of lower body strength in community-residing older adults. Res. Q. Exerc. Sport 1999, 70, 113–119. [Google Scholar] [CrossRef]
- Allali, G.; Montembeault, M.; Griffa, A.; Beauchet, O. Default mode network and the timed up and go in MCI: A structural covariance analysis. Exp. Gerontol. 2020, 129, 110748. [Google Scholar] [CrossRef]
- Nordin, E.; Rosendahl, E.; Lundin-Olsson, L. Timed “Up & Go” test: Reliability in older people dependent in activities of daily living--focus on cognitive state. Phys. Ther. 2006, 86, 646–655. [Google Scholar]
- Telenius, E.W.; Engedal, K.; Bergland, A. Inter-rater reliability of the Berg Balance Scale, 30 s chair stand test and 6 m walking test, and construct validity of the Berg Balance Scale in nursing home residents with mild-to-moderate dementia. BMJ Open 2015, 5, e008321. [Google Scholar] [CrossRef]
- Muir-Hunter, S.W.; Graham, L.; Montero Odasso, M. Reliability of the Berg Balance Scale as a Clinical Measure of Balance in Community-Dwelling Older Adults with Mild to Moderate Alzheimer Disease: A Pilot Study. Physiother. Can. 2015, 67, 255–262. [Google Scholar] [CrossRef]
- Popović, R.; Aleksić, A.; Stojanović, D.; Stefanović, M.; Božić, S.; Popović, M. Evaluation of the Physical Fitness Level in Physical Education Female Students Using “Eurofit-Test”. Int. J. Sports Sci. Phys. Educ. 2017, 2, 1–15. [Google Scholar] [CrossRef]
- Varela, S.; Ayán, C.; Cancela, J.M.; Martín, V. Effects of two different intensities of aerobic exercise on elderly people with mild cognitive impairment: A randomized pilot study. Clin. Rehabil. 2012, 26, 442–450. [Google Scholar] [CrossRef]
- Henry, J.D.; Crawford, J.R. A meta-analytic review of verbal fluency deficits in depression. J. Clin. Exp. Neuropsychol. 2005, 27, 78–101. [Google Scholar] [CrossRef]
- Salmon, D.P.; Bondi, M.W. Neuropsychological assessment of dementia. Annu. Rev. Psychol. 2009, 60, 257–282. [Google Scholar] [CrossRef]
- Taler, V.; Phillips, N.A. Language performance in Alzheimer’s disease and mild cognitive impairment: A comparative review. J. Clin. Exp. Neuropsychol. 2008, 30, 501–556. [Google Scholar] [CrossRef]
- Bowie, C.R.; Harvey, P.D. Administration and interpretation of the Trail Making Test. Nat. Protoc. 2006, 1, 2277–2281. [Google Scholar] [CrossRef]
- McMorris, T.; Hale, B.J. Differential effects of differing intensities of acute exercise on speed and accuracy of cognition: A meta-analytical investigation. Brain Cogn. 2012, 80, 338–351. [Google Scholar] [CrossRef]
- Arbuthnott, K.; Frank, J. Trail Making Test, Part B as a measure of executive control: Validation using a set-switching paradigm. J. Clin. Exp. Neuropsychol. 2000, 22, 518–528. [Google Scholar] [CrossRef]
- Sánchez-Cubillo, I.; Periáñez, J.A.; Adrover-Roig, D.; Rodríguez-Sánchez, J.; Ríos-Lago, M.; Tirapu, J.; Barceló, F. Construct validity of the Trail Making Test: Role of task-switching, working memory, inhibition/interference control, and visuomotor abilities. J. Int. Neuropsychol. Soc. 2009, 15, 438–450. [Google Scholar] [CrossRef]
- Lim, J.; Dinges, D.F. Sleep deprivation and vigilant attention. In Annals of the New York Academy of Sciences; Blackwell Publishing Inc.: Malden, MA, USA, 2008; pp. 305–322. [Google Scholar]
- Basner, M.; Dinges, D.F. Maximizing sensitivity of the psychomotor vigilance test (PVT) to sleep loss. Sleep 2011, 34, 581–591. [Google Scholar] [CrossRef]
- Langner, R.; Eickhoff, S.B. Sustaining attention to simple tasks: A meta-analytic review of the neural mechanisms of vigilant attention. Psychol. Bull. 2013, 139, 870. [Google Scholar] [CrossRef]
- Chang, Y.K.; Labban, J.D.; Gapin, J.I.; Etnier, J.L. The effects of acute exercise on cognitive performance: A meta-analysis. Brain Res. 2012, 1453, 87–101. [Google Scholar] [CrossRef]
- Krootnark, K.; Chaikeeree, N.; Saengsirisuwan, V.; Boonsinsukh, R. Effects of low-intensity home-based exercise on cognition in older persons with mild cognitive impairment: A direct comparison of aerobic versus resistance exercises using a randomized controlled trial design. Front. Med. 2024, 11, 1392429. [Google Scholar] [CrossRef]
- Shu, W.; Chen, L.; Qiu, J.; Kim, S.M. Effects of aerobic exercise interventions on cognitive function, sleep quality, and quality of life in older adults with mild cognitive impairment: A systematic review and meta-analysis. Front. Neurol. 2025, 16, 1693052. [Google Scholar] [CrossRef]
- Bardopoulou, M.S.; Patsaki, I.; Chondronikola, C.; Chryssanthopoulos, C.; Cherouveim, E.D.; Lakoniti, K.-O.; Maridaki, M.; Papageorgiou, S.G.; Koutsilieris, M.; Philippou, A. Effect of a 36-Week Supervised Exercise Training Program on Physical and Cognitive Function in Older Patients with Dementia. In Vivo 2024, 38, 286–294. [Google Scholar] [CrossRef]





| Variable | Mean ± SE/n (%) |
|---|---|
| Number of participants | 17 |
| Age (years) | 65.5 ± 2.15 |
| Sex (female/male) | 10 (59%)/7 (41%) |
| Body mass (kg) | 74.5 ± 3.42 |
| Height (cm) | 168 ± 0.02 |
| BMI (kg/m2) | 26.4 ± 1.14 |
| Diagnosis | MCI: n = 13/eAD: n = 4 |
| CDR score | MCI ≤ 0.5/eAD ≤ 1 |
| Education (years) | 11.7 ± 0.8 |
| Variables | CON | HVI | CA |
|---|---|---|---|
| MoCA 5-word Delayed Recall | −0.12 ± 0.22 | 1.24 ± 0.29 * | 1.12 ± 0.30 ** |
| MoCA 5-word Delayed Recall Category Cue | 0.12 ± 0.19 | −0.65 ± 0.32 | −0.88 ± 0.28 * |
| MoCA Total | 0.71 ± 0.51 | 3.41 ± 0.51 * | 2.06 ± 0.52 |
| FAB Luria Motor | −0.12 ± 0.08 | 0.35 ± 0.12 * | 0.18 ± 0.15 |
| FAB Go-No-Go | −0.12 ± 0.19 | 0.65 ± 0.19 | 0.41 ± 0.17 * |
| FAB Total | −0.18 ± 0.23 | 1.65 ± 0.38 ** | 1.0 ± 0.33 * |
| Semantic Fluency | 0.00 ± 0.61 | 2.12 ± 0.48 | 0.82 ± 0.70 |
| TMT-A | −24.42 ± 16.88 | −34.38 ± 12.28 | −27.13 ± 11.04 |
| TMT-B | 22.41 ± 15.93 | −18.59 ± 6.63 | −14.68 ± 6.47 |
| PVT Reaction Time | 0.12 ± 0.56 | 0 ± 0.62 | −0.29 ± 0.68 |
| PVT False Response | 0 ± 0.15 | −0.06 ± 0.16 | 0.12 ± 0.15 |
| PVT Mean Response | −11.76 ± 55.84 | 83.94 ± 44.28 | 30.35 ± 41.18 |
| PVT Number of Attempts | 0.59 ± 1.50 | 0.12 ± 1.19 | −0.59 ± 0.54 |
| Variables | CON | HVI | CA |
|---|---|---|---|
| HG | 0.08 ± 0.57 | 1.16 ± 0.42 | 0.40 ± 0.27 |
| 30s STS | 0.7 ± 0.7 | 2.2 ± 0.3 | 1.7 ± 0.4 |
| TUG | 0.09 ± 0.17 | −0.35 ± 0.19 | −0.22 ± 0.13 |
| PTT | −0.58 ± 0.55 | −1.48 ± 0.46 | −0.78 ± 0.44 |
| BBS | 0.1 ± 0.1 | 0.3 ± 0.2 | 0.0 ± 0.2 |
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Bardopoulou, M.; Chryssanthopoulos, C.; Cherouveim, E.D.; Tzeravini, E.; Stanitsa, E.; Koustimpi, M.; Chatzinikita, E.; Patsaki, I.; Poulos, S.; Papatriantafyllou, J.; et al. Acute Effects of High-Velocity Interval Cycling Versus Continuous Moderate-Intensity Cycling on Cognitive Function in Patients with Mild Cognitive Impairment. Brain Sci. 2026, 16, 342. https://doi.org/10.3390/brainsci16030342
Bardopoulou M, Chryssanthopoulos C, Cherouveim ED, Tzeravini E, Stanitsa E, Koustimpi M, Chatzinikita E, Patsaki I, Poulos S, Papatriantafyllou J, et al. Acute Effects of High-Velocity Interval Cycling Versus Continuous Moderate-Intensity Cycling on Cognitive Function in Patients with Mild Cognitive Impairment. Brain Sciences. 2026; 16(3):342. https://doi.org/10.3390/brainsci16030342
Chicago/Turabian StyleBardopoulou, Mari, Costas Chryssanthopoulos, Evgenia D. Cherouveim, Evangelia Tzeravini, Evangelia Stanitsa, Maria Koustimpi, Eirini Chatzinikita, Irini Patsaki, Stelios Poulos, John Papatriantafyllou, and et al. 2026. "Acute Effects of High-Velocity Interval Cycling Versus Continuous Moderate-Intensity Cycling on Cognitive Function in Patients with Mild Cognitive Impairment" Brain Sciences 16, no. 3: 342. https://doi.org/10.3390/brainsci16030342
APA StyleBardopoulou, M., Chryssanthopoulos, C., Cherouveim, E. D., Tzeravini, E., Stanitsa, E., Koustimpi, M., Chatzinikita, E., Patsaki, I., Poulos, S., Papatriantafyllou, J., Vassilakopoulos, T., Maridaki, M., Consoulas, C., Papageorgiou, S. G., Koutsilieris, M., & Philippou, A. (2026). Acute Effects of High-Velocity Interval Cycling Versus Continuous Moderate-Intensity Cycling on Cognitive Function in Patients with Mild Cognitive Impairment. Brain Sciences, 16(3), 342. https://doi.org/10.3390/brainsci16030342

