IJPR.2026.139
Type of Article: Original Research
Volume 14; Issue 3 (August 2026)
Page No.: 5008-5014
DOI: https://dx.doi.org/10.16965/ijpr.2026.139
Effect of Speed Intensive Gait Training on Balance, Gait Speed, and Endurance in Patients with Chemotherapy-Induced Peripheral Neuropathy
Geetu Vikram Ahuja *1, Sabah Thaver 2, Ali Irani 3.
*1 Post Graduate Student, School of Physiotherapy, NMIMS, (deemed to be) University, Vile Parle, Mumbai, India. ORCiD: 0009-0005-0858-4455
2 Assistant Professor, School of Physiotherapy, NMIMS (deemed to be) University, Vile Parle, Mumbai, India.
3 HOD, Physiotherapy, Sports Medicine & Rehabilitation, Nanavati Max Super Speciality Hospital, Vile Parle, Mumbai, India.
Corresponding Author: Dr. Geetu Vikram Ahuja, Post Graduate Student, School of Physiotherapy, NMIMS, (deemed to be) University, Vile Parle, Mumbai, India. E-Mail: geetuvahuja@gmail.com
ABSTRACT
Background: Chemotherapy-induced peripheral neuropathy (CIPN) is a common complication of neurotoxic chemotherapy and is associated with sensory deficits, impaired balance, reduced gait speed, and decreased endurance, resulting in reduced functional mobility and increased fall risk. Exercise-based rehabilitation interventions have shown promise in improving functional outcomes in individuals with CIPN. This study aimed to compare the effects of treadmill training and speed-intensive gait training on balance, gait speed, and walking endurance in individuals with CIPN.
Methodology: A randomized controlled trial was conducted on 46 individuals diagnosed with chemotherapy-induced peripheral neuropathy. Participants were randomly allocated into two groups: Group 1 received balance training combined with treadmill training, while Group 2 received balance training combined with speed-intensive gait training. Both groups underwent supervised intervention for four weeks. Outcome measures included the Mini-Balance Evaluation Systems Test (MiniBESTest), 10-Meter Walk Test (10MWT), and 6-Minute Walk Test (6MWT). Data were analysed using SPSS version 27. Paired t-tests and independent t-tests were used for intra-group and inter-group comparisons, respectively, with the level of significance set at p<0.05.
Results: Both groups demonstrated statistically significant improvements in balance, gait speed, and walking endurance following the intervention (p<0.001). Significant improvements were observed in MiniBESTest scores, self-selected and fast gait speeds, and 6MWT distances in both groups. However, no statistically significant differences were observed between the groups following the intervention.
Conclusion: Both treadmill training and speed-intensive gait training, when combined with balance training, were effective in improving balance, gait speed, and walking endurance in individuals with chemotherapy-induced peripheral neuropathy. Speed-intensive gait training may serve as a practical alternative to treadmill training in settings where access to treadmill equipment is limited.
Keywords: Chemotherapy-Induced Peripheral Neuropathy, CIPN, Treadmill Training, Speed-Intensive Gait Training, Balance, Gait Speed, Endurance.
REFERENCES
[1]. Jena, D., Padhi, B. K., Zahiruddin, Q. S., Ballal, S., Kumar, S., Bhat, M., Sharma, S., Kumar, M. R., Rustagi, S., Gaidhane, A. M., Gaur, A., Sah, S., & Satapathy, P. Estimation of burden of cancer incidence and mortality in India: Based on global burden of disease study 1990-2021. BMC Cancer,2024;24(1):1278.
https://doi.org/10.1186/s12885-024-13035-6
PMid:39407152 PMCid:PMC11476122
[2]. Chen, X., Gan, Y., Au, N. P. B., & Ma, C. H. E. (2024). Current understanding of the molecular mechanisms of chemotherapy-induced peripheral neuropathy. Frontiers in Molecular Neuroscience, 2024;17:1345811.
https://doi.org/10.3389/fnmol.2024.1345811
PMid:38660386 PMCid:PMC11039947
[3]. Mazilu, L. Incidence of chemotherapy-induced peripheral neuropathy in cancer patients in clinical practice. Farmacia, 2019;67:472-476.
https://doi.org/10.31925/farmacia.2019.3.14
[4]. Chung, K. H., Park, S. B., Streckmann, F., Wiskemann, J., Mohile, N., Kleckner, A. S., Colloca, L., Dorsey, S. G., & Kleckner, I. R. Mechanisms, mediators, and moderators of the effects of exercise on chemotherapy-induced peripheral neuropathy. Cancers, 2022;14(5):1224.
https://doi.org/10.3390/cancers14051224
PMid:35267533 PMCid:PMC8909585
[5]. Mattar, M., Umutoni, F., Hassan, M. A., Wamburu, M. W., Turner, R., Patton, J. S., Chen, X., & Lei, W. Chemotherapy-induced peripheral neuropathy: A recent update on pathophysiology and treatment. Life, 2024;14(8):991.
https://doi.org/10.3390/life14080991
PMid:39202733 PMCid:PMC11355765
[6]. Stoller, S., Capozza, S., Alberti, P., Lustberg, M., & Kleckner, I. R. Framework to leverage physical therapists for the assessment and treatment of chemotherapy-induced peripheral neurotoxicity (CIPN). Supportive Care in Cancer, 2023;31(5):293.
https://doi.org/10.1007/s00520-023-07734-2
PMid:37086308 PMCid:PMC11552664
[7]. Park, S. B., Tamburin, S., Schenone, A., Kleckner, I. R., Velasco, R., Alberti, P., Kanzawa-Lee, G., Lustberg, M., Dorsey, S. G., Mantovani, E., Hamedani, M., Argyriou, A. A., Cavaletti, G., Hoke, A., & Toxic Neuropathy Consortium. Optimal outcome measures for assessing exercise and rehabilitation approaches in chemotherapy-induced peripheral neurotoxicity: Systematic review and consensus expert opinion. Expert Review of Neurotherapeutics, 2022;22(1):65-76.
https://doi.org/10.1080/14737175.2022.2018300
PMid:34894974 PMCid:PMC8963967
[8]. Lee, K. T., Bulls, H. W., Hoogland, A. I., James, B. W., Colon-Echevarria, C. B., & Jim, H. S. L. Chemotherapy-induced peripheral neuropathy (CIPN): A narrative review and proposed theoretical model. Cancers, 2024;16(14):2571.
https://doi.org/10.3390/cancers16142571
PMid:39061210 PMCid:PMC11274737
[9]. Colvin, L. A. Chemotherapy-induced peripheral neuropathy: Where are we now? Pain, 2019;160(Suppl 1):S1-S10.
https://doi.org/10.1097/j.pain.0000000000001540
PMid:31008843 PMCid:PMC6499732
[10]. Kleckner, I. R., Manuweera, T., Lin, P. J., Chung, K. H., Kleckner, A. S., Gewandter, J. S., Culakova, E., Tivarus, M. E., Dunne, R. F., Loh, K. P., Mohile, N. A., Kesler, S. R., & Mustian, K. M. Pilot trial testing the effects of exercise on chemotherapy-induced peripheral neurotoxicity (CIPN) and the interoceptive brain system. Research Square. 2024; Advance online publication.
https://doi.org/10.21203/rs.3.rs-4022351/v1
[11]. Kneis, S., Wehrle, A., Müller, J., Maurer, C., Ihorst, G., Gollhofer, A., & Bertz, H. It’s never too late: Balance and endurance training improves functional performance, quality of life, and alleviates neuropathic symptoms in cancer survivors suffering from chemotherapy-induced peripheral neuropathy: Results of a randomized controlled trial. BMC Cancer, 2019;19(1):414.
https://doi.org/10.1186/s12885-019-5522-7
PMid:31046719 PMCid:PMC6498676
[12]. Lamontagne, A., & Fung, J. Faster is better: Implications for speed-intensive gait training after stroke. Stroke, 2024;35(11):2543-2548.
https://doi.org/10.1161/01.STR.0000144685.88760.d7
PMid:15472095
[13]. Sparrow, D., DeAngelis, T. R., Hendron, K., Thomas, C. A., Saint-Hilaire, M., & Ellis, T. Highly challenging balance program reduces fall rate in Parkinson disease. Journal of Neurologic Physical Therapy, 2016;40(1):24-30.
https://doi.org/10.1097/NPT.0000000000000111
PMid:26655100 PMCid:PMC4681297
[14]. Horak FB. Postural orientation and equilibrium: what do we need to know about neural control of balance to prevent falls? Age Ageing. 2006;35(Suppl 2):ii7-ii11.
https://doi.org/10.1093/ageing/afl077
PMid:16926210 PMCid:PMC7857621
[15]. Monfort SM, Pan X, Patrick R, Ramaswamy B, Wesolowski R, Naughton MJ, et al. Gait, balance, and patient-reported outcomes during taxane-based chemotherapy in early-stage breast cancer patients. Breast Cancer Res Treat. 2017;164(1):69-77.
https://doi.org/10.1007/s10549-017-4230-8
PMid:28374323 PMCid:PMC5510549
[16]. Schwenk M, Schmidt M, Pfisterer M, Oster P, Hauer K. Interactive sensor-based balance training in older cancer patients with chemotherapy-induced peripheral neuropathy: a randomized controlled trial. J Cancer Surviv. 2016;10(2):317-324.
https://doi.org/10.1159/000442253
PMid:26678611 PMCid:PMC6644035
[17]. Kleckner IR, Kamen C, Gewandter JS, Mohile NA, Heckler CE, Culakova E, et al. Effects of exercise during chemotherapy on chemotherapy-induced peripheral neuropathy: a multicenter randomized controlled trial. Support Care Cancer. 2018;26(4):1019-1028.
https://doi.org/10.1007/s00520-017-4013-0
PMid:29243164 PMCid:PMC5823751
[18]. Kleim JA, Jones TA. Principles of experience-dependent neural plasticity: implications for rehabilitation after brain damage. J Speech Lang Hear Res. 2008;51(1):S225-S239.
https://doi.org/10.1044/1092-4388(2008/018)
PMid:18230848
[19]. Peterka RJ. Sensorimotor integration in human postural control. J Neurophysiol. 2002;88(3):1097-1118.
https://doi.org/10.1152/jn.2002.88.3.1097
PMid:12205132
[20]. Dietz V. Spinal cord pattern generators for locomotion. Clin Neurophysiol. 2003;114(8):1379-1389.
https://doi.org/10.1016/S1388-2457(03)00120-2
PMid:12888019
[21]. Hornby TG, Campbell DD, Zemon DH, Kahn JH. Clinical and quantitative evaluation of robotic-assisted treadmill walking to retrain ambulation after spinal cord injury. Top Spinal Cord Inj Rehabil. 2005;11(2):1-17.
https://doi.org/10.1310/14Q9-AD7M-FXX9-1G2J
[22]. Langhorne P, Bernhardt J, Kwakkel G. Stroke rehabilitation. Lancet. 2011;377(9778):1693-1702.
https://doi.org/10.1016/S0140-6736(11)60325-5
PMid:21571152
[23]. Carr JH, Shepherd RB. Neurological Rehabilitation: Optimizing Motor Performance. 2nd ed. Edinburgh: Churchill Livingstone Elsevier; 2010.
[24]. Winters-Stone KM, Horak F, Jacobs PG, Trubowitz P, Dieckmann NF, Stoyles S, et al. Falls, functioning, and disability among women with persistent symptoms of chemotherapy-induced peripheral neuropathy. J Clin Oncol. 2017;35(23):2604-2612.
https://doi.org/10.1200/JCO.2016.71.3552
PMid:28586243 PMCid:PMC5549452
[25]. Plowman SA, Smith DL. Exercise Physiology for Health, Fitness, and Performance. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2013.








