Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Scientific Reports
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. scientific reports
  3. articles
  4. article
High intensity functional training versus traditional resistance training effects on inflammatory, metabolic, and physical outcomes in overweight men a randomized controlled trial
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 21 February 2026

High intensity functional training versus traditional resistance training effects on inflammatory, metabolic, and physical outcomes in overweight men a randomized controlled trial

  • Fatemehsadat Hosseini Moshkenani1,
  • Shervin Abedi1,
  • Fatemeh Shabkhiz1,
  • Rahman Soori1 &
  • …
  • Nafiseh Esmaeil2 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Diseases
  • Endocrinology
  • Health care
  • Medical research
  • Physiology

Abstract

Overweight and obesity are major global health concerns linked to chronic diseases. This study compared the effects of high-intensity functional training (HIFT) and resistance training (RT) on metabolic, inflammatory, and physical markers in overweight men. Thirty-four overweight men (31.91 ± 2.44 years, BMI 27.78 ± 1.47 kg/m2) were assigned to the HIFT (n = 13), RT (n = 10), and control (n = 11) groups. The HIFT included four sets of 30-second exercises at 30% 1RM, whereas the RT involved three sets of 12 repetitions at 70% 1RM. Both interventions were performed thrice weekly for eight weeks. Blood samples were collected before and after training to assess the levels of inflammatory markers (IL-4, γ-IFN, MMP-9 and TLR4) and metabolic markers (FBS, LDL, HDL, triglycerides and cholesterol). Body composition and performance were evaluated. No significant differences in inflammatory markers were detected between the groups. HIFT and RT significantly reduced fasting blood sugar (p < 0.05). RT lowered total cholesterol, whereas triglycerides decreased in both groups. Skeletal muscle mass increased significantly. Compared with RT, HIFT led to greater body fat reduction, although both improved from baseline. Both groups had increased 1RM bench press strength. Compared with RT and the control, HIFT significantly increased VO2max, whereas RT improved VO2max compared with the control. HIFT is a promising approach for managing overweight and obesity, particularly for enhancing cardiovascular fitness and body composition.

Trial registration IRCT.ir, IRCT20170724035269N2, registered on 27/05/2025. This study was retrospectively registered.

Similar content being viewed by others

Evaluating the impact of exercise on intermediate disease markers in overweight and obese individuals through a network meta-analysis of randomized controlled trials

Article Open access 27 May 2024

High-intensity interval training improves bone remodeling, lipid profile, and physical function in multiple sclerosis patients

Article Open access 13 July 2024

The effects of combined exercise training on glucose metabolism and inflammatory markers in sedentary adults: a systematic review and meta-analysis

Article Open access 22 January 2024

Data availability

The datasets generated and/or analysed during the current study are not publicly available due to participant privacy and confidentiality considerations but are available from the corresponding author on reasonable request. All shared data will be fully de-identified to protect participant privacy.

References

  1. Tabarés Seisdedos, R. Health effects of overweight and obesity in 195 countries over 25 years (2017).

  2. Rogero, M. M. & Calder, P. C. Obesity, inflammation, toll-like receptor 4 and fatty acids. Nutrients 10(4), 432 (2018).

    Google Scholar 

  3. Ayatollahi, S. & Ghoreshizadeh, Z. Prevalence of obesity and overweight among adults in Iran. Obes. Rev. 11(5), 335–337 (2010).

    Google Scholar 

  4. Campos-Bayardo, T. I. et al. The role of TLRs in obesity and its related metabolic disorders. Int. J. Mol. Sci. 26(5), 2229 (2025).

  5. Gleeson, M. et al. The anti-inflammatory effects of exercise: Mechanisms and implications for the prevention and treatment of disease. Nat. Rev. Immunol. 11(9), 607–615 (2011).

    Google Scholar 

  6. Hotamisligil, G. S. Inflammation, metaflammation and immunometabolic disorders. Nature 542(7640), 177–185 (2017).

    Google Scholar 

  7. Shi, H. et al. TLR4 links innate immunity and fatty acid–induced insulin resistance. J. Clin. Investig. 116(11), 3015–3025 (2006).

    Google Scholar 

  8. Orr, J. S. et al. Toll-like receptor 4 deficiency promotes the alternative activation of adipose tissue macrophages. Diabetes 61(11), 2718–2727 (2012).

    Google Scholar 

  9. Ahmad, R. et al. Elevated expression of the toll like receptors 2 and 4 in obese individuals: Its significance for obesity-induced inflammation. J. Inflamm. 9(1), 48 (2012).

    Google Scholar 

  10. Langjahr, P. et al. Metalloproteinase-dependent TLR2 ectodomain shedding is involved in soluble toll-like receptor 2 (sTLR2) production. PloS One 9(12), e104624 (2014).

    Google Scholar 

  11. Jaoude, J. & Koh, Y. Matrix metalloproteinases in exercise and obesity. Vasc. Health Risk Manag. 287, 95 (2016).

    Google Scholar 

  12. Wensveen, F. M., Valentić, S., Šestan, M., Turk Wensveen, T. & Polić, B. The big Bang in obese fat: Events initiating obesity-induced adipose tissue inflammation. Eur. J. Immunol. 45(9), 2446–2456 (2015).

    Google Scholar 

  13. Lumeng, C. N., Bodzin, J. L. & Saltiel, A. R. Obesity induces a phenotypic switch in adipose tissue macrophage polarization. J. Clin. Investig. 117(1), 175–184 (2007).

    Google Scholar 

  14. Soltani, N., Marandi, S. M., Kazemi, M. & Esmaeil, N. Combined all-extremity high-intensity interval training regulates immunometabolic responses through toll-like receptor 4 adaptors and A20 downregulation in obese young females. Obes. Facts 13(3), 415–431 (2020).

    Google Scholar 

  15. Filipovic, T. et al. Research article effects of 12-week exercise program on enzyme activity of serum matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in female patients with postmenopausal osteoporosis: A randomized control study (2020).

  16. Lee, M-G., Park, K-S., Kim, D-U., Choi, S-M. & Kim, H-J. Effects of high-intensity exercise training on body composition, abdominal fat loss, and cardiorespiratory fitness in middle-aged Korean females. Appl. Physiol. Nutr. Metab. 37(6), 1019–1027 (2012).

    Google Scholar 

  17. Nikseresht, M. Comparison of serum cytokine levels in men who are obese or men who are lean: Effects of nonlinear periodized resistance training and obesity. J. Strength Cond. Res. 32(6), 1787–1795 (2018).

    Google Scholar 

  18. Kim, E. S. et al. Improved insulin sensitivity and adiponectin level after exercise training in obese Korean youth. Obesity 15(12), 3023–3030 (2007).

    Google Scholar 

  19. Atashak, S. et al. High-intensity interval training improves lipocalin-2 and omentin-1 levels in men with obesity. Int. J. Sports Med. 43(04), 328–335 (2022).

    Google Scholar 

  20. Tayebi, S. M., Ghanbari-Niaki, A., Saeidi, A. & Hackney, A. C. Exercise training, neuregulin 4 and obesity. Ann. Appl. Sport Sci. 5(2), 1 (2017).

    Google Scholar 

  21. Saeidi, A. et al. Astaxanthin supplemented with high-intensity functional training decreases adipokines levels and cardiovascular risk factors in men with obesity. Nutrients 15(2), 286 (2023).

    Google Scholar 

  22. Supriya, R. et al. Spirulina supplementation with high-intensity interval training decreases adipokines levels and cardiovascular risk factors in men with obesity. Nutrients 15(23), 4891 (2023).

    Google Scholar 

  23. Feito, Y., Heinrich, K. M., Butcher, S. J. & Poston, W. S. C. High-intensity functional training (HIFT): Definition and research implications for improved fitness. Sports 6(3), 76 (2018).

    Google Scholar 

  24. Murawska-Cialowicz, E., Wojna, J. & Zuwala-Jagiello, J. Crossfit training changes brain-derived neurotrophic factor and Irisin levels at rest, after wingate and progressive tests, and improves aerobic capacity and body composition of young physically active men and women. J. Physiol. Pharmacol. 66(6), 811–821 (2015).

    Google Scholar 

  25. NSCA Science of Strength & Conditioning. Essentials of strength training and conditioning: Human kinetics (2021).

  26. McDougle, J. M., Mangine, G. T., Townsend, J. R., Jajtner, A. R. & Feito, Y. Acute physiological outcomes of high-intensity functional training: A scoping review. PeerJ 11, e14493 (2023).

    Google Scholar 

  27. Santos, D. A. T. et al. Comparison of physiological and psychobiological acute responses between high intensity functional training and high intensity continuous training. Sports Med. Health Sci. 7(1), 68–76 (2025).

    Google Scholar 

  28. Borga, M. et al. Advanced body composition assessment: From body mass index to body composition profiling. J. Invest. Med. 66(5), 1–9 (2018).

    Google Scholar 

  29. Zhang, F. L. et al. Strong association of waist circumference (WC), body mass index (BMI), waist-to-height ratio (WHtR), and waist-to-hip ratio (WHR) with diabetes: A population-based cross-sectional study in Jilin Province, China. J. Diabetes Res. 2021, 8812431 (2021).

    Google Scholar 

  30. Riebe, D., Ehrman, J., Liguori, G. & Magal, M. ACSM’s Guidelines for Exercise Testing and Prescription 226–363 (2018).

  31. Buttar, K., Scholar, Saboo, N. & Kacker, S. A review: Maximal oxygen uptake (VO2 max) and its estimation methods. Int. J. Phys. Educ. Sports Health 6(6), 24–32 (2019).

  32. Pournot, H. et al. Time-course of changes in inflammatory response after whole-body cryotherapy multi exposures following severe exercise. PloS One 6(7), e22748 (2011).

    Google Scholar 

  33. Soltani, N., Marandi, S. M., Kazemi, M. & Esmaeil, N. Meta-inflammatory state and insulin resistance can improve after 10 weeks of combined all-extremity high-intensity interval training in sedentary overweight/obese females: A quasi-experimental study. J. Diabetes Metab. Disord. 19(2), 717–726 (2020).

    Google Scholar 

  34. Bastarache, J. A. et al. Accuracy and reproducibility of a multiplex immunoassay platform: A validation study. J. Immunol. Methods 367(1–2), 33–39 (2011).

    Google Scholar 

  35. Leng, S. X. et al. ELISA and multiplex technologies for cytokine measurement in inflammation and aging research. J. Gerontol. Ser. A Biol. Sci. Med. Sci. 63(8), 879–884 (2008).

    Google Scholar 

  36. Favere, K. et al. A systematic literature review on the effects of exercise on human toll-like receptor expression. Exerc. Immunol. Rev. 27, 84–124 (2021).

    Google Scholar 

  37. Church, T. S. et al. Effects of aerobic and resistance training on hemoglobin A1c levels in patients with type 2 diabetes: A randomized controlled trial. Jama 304(20), 2253–2262 (2010).

    Google Scholar 

  38. Jelleyman, C. et al. The effects of high-intensity interval training on glucose regulation and insulin resistance: A meta-analysis. Obes. Rev. 16(11), 942–961 (2015).

    Google Scholar 

  39. Schulz, K. F., Altman, D. G. & Moher, D. CONSORT 2010 statement: Updated guidelines for reporting parallel group randomised trials. BMJ 340, c332 (2010).

    Google Scholar 

  40. Robinson, E. et al. Short-term high-intensity interval and moderate-intensity continuous training reduce leukocyte TLR4 in inactive adults at elevated risk of type 2 diabetes. J. Appl. Physiol. 119(5), 508 –516 (2015).

  41. Soltani, N. et al. Assessment of the effect of short-term combined high-intensity interval training on TLR4, NF-κB and IRF3 expression in young overweight and obese girls. Public. Health Genomics 23(1–2), 26–36 (2020).

    Google Scholar 

  42. Reyna, S. M. et al. Short-term exercise training improves insulin sensitivity but does not inhibit inflammatory pathways in immune cells from insulin-resistant subjects. J. Diabetes Res. 2013, 107805 (2013).

    Google Scholar 

  43. Phillips, M. D. et al. Resistance training reduces subclinical inflammation in obese, postmenopausal women. Med. Sci. Sports. Exerc. 44(11), 2099–2110 (2012).

    Google Scholar 

  44. Oliveira-Child, M., Leggate, M. & Gleeson, M. Effects of two weeks of high-intensity interval training (HIIT) on monocyte TLR2 and TLR4 expression in high BMI sedentary men. Int. J. Exerc. Sci. 6, 81–90 (2013).

    Google Scholar 

  45. Silveira, L. S. et al. Macrophage polarization: Implications on metabolic diseases and the role of exercise. Crit. Rev. Eukaryot. Gene Expr. 26(2), 115–132 (2016).

    Google Scholar 

  46. Franceschi, C., Garagnani, P., Parini, P., Giuliani, C. & Santoro, A. Inflammaging: A new immune-metabolic viewpoint for age-related diseases. Nat. Rev. Endocrinol. 14(10), 576–590 (2018).

    Google Scholar 

  47. Rodriguez-Miguelez, P. et al. Role of Toll-like receptor 2 and 4 signaling pathways on the inflammatory response to resistance training in elderly subjects. Age 36(6), 9734 (2014).

    Google Scholar 

  48. Gleeson, M. Immune function in sport and exercise. J. Appl. Physiol. (2007).

  49. Petersen, A. M. W. & Pedersen, B. K. The anti-inflammatory effect of exercise. J. Appl. Physiol. 98(4), 1154–1162 (2005).

    Google Scholar 

  50. Egan, B. & Zierath, J. R. Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metabol. 17(2), 162–184 (2013).

    Google Scholar 

  51. Handschin, C. & Spiegelman, B. M. The role of exercise and PGC1α in inflammation and chronic disease. Nature 454(7203), 463–469 (2008).

    Google Scholar 

  52. Hotamisligil, G. S. Inflammation and metabolic disorders. Nature 444(7121), 860–867 (2006).

    Google Scholar 

  53. Cani, P. D. et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes 56(7), 1761–1772 (2007).

    Google Scholar 

  54. Jackson, L., Cady, C. T. & Cambier, J. C. TLR4-mediated signaling induces MMP9-dependent cleavage of B cell surface CD23. J. Immunol. 183(4), 2585–2592 (2009).

  55. Lo Presti, R., Hopps, E. & Caimi, G. Gelatinases and physical exercise: A systematic review of evidence from human studies. Medicine 96(37), e8072 (2017).

    Google Scholar 

  56. Filipović, T. et al. Effects of 12-Week exercise program on enzyme activity of serum matrix Metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in female patients with postmenopausal osteoporosis: A randomized control study. Biomed. Res. Int. 2020, 9758289 (2020).

    Google Scholar 

  57. Rullman, E., Olsson, K., Wågsäter, D. & Gustafsson, T. Circulating MMP-9 during exercise in humans. Eur. J. Appl. Physiol. 113(5), 1249–1255 (2013).

    Google Scholar 

  58. Smith, J. S., Bellissimo, G. F. & Amorim, F. T. The physiological responses to volume-matched high-intensity functional training protocols with varied time domains. Front. Physiol. 15, 1511961 (2024).

    Google Scholar 

  59. Prestes, J. et al. The effects of muscle strength responsiveness to periodized resistance training on resistin, leptin, and cytokine in elderly postmenopausal women. J. Strength. Conditioning Res. 32(1), 113–120 (2018).

    Google Scholar 

  60. Kjølhede, T. et al. Acute and chronic cytokine responses to resistance exercise and training in people with multiple sclerosis. Scand. J. Med. Sci. Sports 26(7), 824–834 (2016).

    Google Scholar 

  61. de Souza, D. C. et al. Effects of high-intensity interval and moderate-intensity continuous exercise on inflammatory, leptin, IgA, and lipid peroxidation responses in obese males. Front. Physiol. 9, 567 (2018).

    Google Scholar 

  62. O’rourke, R. et al. Depot-specific differences in inflammatory mediators and a role for NK cells and IFN-γ in inflammation in human adipose tissue. Int. J. Obes. 33(9), 978–990 (2009).

    Google Scholar 

  63. Goossens, G. H. The metabolic phenotype in obesity: Fat mass, body fat distribution, and adipose tissue function. Obes. Facts 10(3), 207–215 (2017).

    Google Scholar 

  64. Kliszczewicz, B., Buresh, R., Bechke, E. & Williamson, C. Metabolic biomarkers following a short and long bout of high-intensity functional training in recreationally trained men (2017).

  65. Yin, M. et al. Is low-volume high-intensity interval training a time-efficient strategy to improve cardiometabolic health and body composition? A meta-analysis. Appl. Physiol. Nutr. Metab. 49(3), 273–292 (2023).

    Google Scholar 

  66. Kapsis, D. P. et al. Changes in body composition and strength after 12 weeks of high-intensity functional training with two different loads in physically active men and women: A randomized controlled study. Sports 10(1), 7 (2022).

    Google Scholar 

  67. Ameur, R. et al. Unlocking the power of synergy: High-intensity functional training and early time-restricted eating for transformative changes in body composition and cardiometabolic health in inactive women with obesity. Plos One 19(5), e0301369 (2024).

    Google Scholar 

  68. Seyed, M. T., Peiman, H., Ayoub, S. & Mohammadreza, F. Intense circuit resistance training along with zataria multifl ora supplementation reduced plasma retinol binding protein-4 and tumor necrosis factor-in postmenopausal females. Jundishapur J. Nat. Pharm. (2018).

  69. Adami, P. et al. Physiological profile comparison between high intensity functional training, endurance and power athletes. Eur. J. Appl. Physiol. 122(2), 531–539 (2022).

    Google Scholar 

  70. Pedersen, B. K. & Febbraio, M. A. Muscle as an endocrine organ: Focus on muscle-derived interleukin-6. Physiol. Rev. (2008).

  71. Laforgia, J., Withers, R. T. & Gore, C. J. Effects of exercise intensity and duration on the excess post-exercise oxygen consumption. J. Sports Sci. 24(12), 1247–1264 (2006).

    Google Scholar 

  72. Fasshauer, M. & Blüher, M. Adipokines in health and disease. Trends Pharmacol. Sci. 36(7), 461–470 (2015).

    Google Scholar 

  73. Lasevicius, T. et al. Effects of different intensities of resistance training with equated volume load on muscle strength and hypertrophy. Eur. J. Sport Sci. 18(6), 772–780 (2018).

    Google Scholar 

  74. Lacio, M. et al. Effects of resistance training performed with different loads in untrained and trained male adult individuals on maximal strength and muscle hypertrophy: A systematic review. Int. J. Environ. Res. Public Health 18(21), 11237 (2021).

    Google Scholar 

  75. Cosgrove, S. J., Crawford, D. A. & Heinrich, K. M. Multiple fitness improvements found after 6-months of high intensity functional training. Sports 7(9), 203 (2019).

    Google Scholar 

  76. Smith, J. S., Bellissimo, G. F. & Amorim, F. T. The physiological responses to volume-matched high-intensity functional training protocols with varied time domains. Front. Physiol. 15, 1511961 (2025).

    Google Scholar 

  77. Ried-Larsen, M., Aarts, H. M. & Joyner, M. J. Effects of strict prolonged bed rest on cardiorespiratory fitness: Systematic review and meta-analysis. J. Appl. Physiol. 123(4), 790–799 (2017).

    Google Scholar 

  78. Astorino, T. A., Mower, M., Flores, A. & Flannery, M. Cardiometabolic response to high intensity functional training versus rowing-based high intensity interval training. Sports Med Health Sci. (2025).

  79. Tomschi, F., Ransmann, P., Schmidt, A. & Hilberg, T. Exercise induced hypoalgesia after a high intensity functional training: A randomized controlled crossover study. BMC Sports Sci. Med. Rehabil. 16(1), 182 (2024).

    Google Scholar 

  80. Klein, S. L. & Flanagan, K. L. Sex differences in immune responses. Nat. Rev. Immunol. 16(10), 626–638 (2016).

    Google Scholar 

Download references

Acknowledgements

The authors would like to acknowledge Dr. Nooshin Lotfi and the staff of the Immunology Department Laboratoryat Isfahan University of Medical Sciences, Iran, particularly Mrs. Fahimeh Hosseininasab, for their kind andinvaluable support.

Funding

This study did not receive external funding and was not supported by any specific grant from funding agencies in the public, commercial, or not-for-profit.

Author information

Authors and Affiliations

  1. Department of Exercise Physiology, Faculty of Physical Education and Sport Sciences, Tehran University, Tehran, Iran

    Fatemehsadat Hosseini Moshkenani, Shervin Abedi, Fatemeh Shabkhiz & Rahman Soori

  2. Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81744, Iran

    Nafiseh Esmaeil

Authors
  1. Fatemehsadat Hosseini Moshkenani
    View author publications

    Search author on:PubMed Google Scholar

  2. Shervin Abedi
    View author publications

    Search author on:PubMed Google Scholar

  3. Fatemeh Shabkhiz
    View author publications

    Search author on:PubMed Google Scholar

  4. Rahman Soori
    View author publications

    Search author on:PubMed Google Scholar

  5. Nafiseh Esmaeil
    View author publications

    Search author on:PubMed Google Scholar

Contributions

F.S.H.M. and S.A. conceptualized and designed the study (this study is based on the master’s thesis of both individuals). F.S.H.M. and N.E. drafted the initial manuscript, conducted the laboratory experiments, and performed the statistical analyses. N.E. also served as an advisor for this project and approved the final manuscript. F.S.H.M. and S.A. conceptualized the study, designed the exercise protocol, and conducted the training sessions. N.E. performed the final editing of the manuscript. F.S. and R.S., as supervisors, oversaw the work and validated the exercise protocol and data. All the authors reviewed and approved the final version of the manuscript.

Corresponding authors

Correspondence to Fatemeh Shabkhiz or Nafiseh Esmaeil.

Ethics declarations

Competing interests

The authors declare no competing interests. This study was reported in accordance with the CONSORT guidelines for randomized controlled trials.

Ethical approval and consent to participate

The study was conducted in accordance with the Declaration of Helsinki and commenced after obtaining ethical approval from the Institutional Review Board of the Faculty of Sport Sciences, University of Tehran (protocol code IR.UT.SPORT.REC.1401.025, approved in July 2022). Informed consent was obtained from all participants prior to enrollment. Due to limited awareness among local researchers regarding international standards for prospective clinical trial registration and the absence of institutional mandates at the time, the trial was registered retrospectively. Following recognition of international requirements, the trial was formally registered without any modifications to the protocol or dataset in the Iranian Registry of Clinical Trials (IRCT.ir; registration code IRCT20170724035269N2) on May 15, 2025. This retrospective registration was authorized and overseen directly by the Vice-Chancellery for Research of the Faculty of Sport Sciences, University of Tehran, ensuring full transparency and integrity of the research process.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hosseini Moshkenani, F., Abedi, S., Shabkhiz, F. et al. High intensity functional training versus traditional resistance training effects on inflammatory, metabolic, and physical outcomes in overweight men a randomized controlled trial. Sci Rep (2026). https://doi.org/10.1038/s41598-026-40482-x

Download citation

  • Received: 09 July 2025

  • Accepted: 13 February 2026

  • Published: 21 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-40482-x

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • High-intensity functional training
  • Traditional resistance training
  • Overweight
  • Metabolic markers
  • Body composition
  • Strength
  • Inflammation
Download PDF

Advertisement

Explore content

  • Research articles
  • News & Comment
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • About Scientific Reports
  • Contact
  • Journal policies
  • Guide to referees
  • Calls for Papers
  • Editor's Choice
  • Journal highlights
  • Open Access Fees and Funding

Publish with us

  • For authors
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Scientific Reports (Sci Rep)

ISSN 2045-2322 (online)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research