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Long-term effects of multimodal prehabilitation and exercise dose\u2013response associations remain unclear. This study aimed to investigate changes in functional capacity and body composition during and after prehabilitation and evaluate exercise dose\u2013response associations.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Data from 816 patients who participated in the monocenter stepped wedge F4S PREHAB trial (March 2021\u2013April 2024) and underwent elective abdominal surgery for gastrointestinal, gynecological, or urological cancers were included. Functional capacity measures included estimated peak oxygen uptake, maximum short exercise capacity, muscle strength (leg press, handgrip), and five-times sit-to-stand test. Body composition measures included weight, fat-free mass, percentage body fat, and phase angle. Assessments occurred at baseline, after prehabilitation, and 3\u00a0months postoperatively. Changes over time and dose\u2013response associations were evaluated with linear mixed models.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Maximum proportions of missing data ranged from 12.9% at preintervention and 24.9% at postintervention to 62.4% after surgery. Significant improvements over time were observed in estimated peak oxygen uptake (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =0.6\u00a0mL\/kg\/min, 95% confidence interval [CI] 0.4\u20130.8), maximum short exercise capacity (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =17.5\u00a0Watt, 95% CI 13.8\u201321.2), leg press (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =18.9\u00a0kg, 95% CI 15.9\u201321.9), handgrip (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =1.1\u00a0kg, 95% CI 0.6\u20131.6), sit-to-stand time (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =0.9\u00a0seconds, 95% CI -1.1 to -0.6), body weight (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =1.1\u00a0kg, 95% CI 0.7\u20131.4), and fat-free mass (\n                      <jats:italic>\u03b2<\/jats:italic>\n                      =0.5\u00a0kg), 95% CI 0.1\u20130.8). Some exercise dose\u2013response associations were found. Functional capacity measures returned to or declined below baseline value. Sensitivity analyses with complete data at follow-up yielded comparable findings with attenuated associations. Associations varied by tumor type, neoadjuvant therapy, malnutrition risk, and training compliance.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Functional capacity and body composition improved after prehabilitation, although gains were generally not sustained postoperatively. Associations may vary between patient subgroups. Future research should focus on targeted approaches and integration with improved postoperative rehabilitation.<\/jats:p>\n                    <jats:p>\n                      <jats:italic>Trial registration<\/jats:italic>\n                      : The F4S PREHAB trial is registered in the International Clinical Trials Registry Platform, NL8699. Registered on 05-06-2020.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1245\/s10434-026-19173-4","type":"journal-article","created":{"date-parts":[[2026,2,23]],"date-time":"2026-02-23T18:33:00Z","timestamp":1771871580000},"page":"5714-5725","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Changes in Functional Capacity and Body Composition After a Multimodal Prehabilitation Program in Patients with Cancer undergoing Abdominal Surgery"],"prefix":"10.1245","volume":"33","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3283-095X","authenticated-orcid":false,"given":"Luuk D.","family":"Drager","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Baukje","family":"van den Heuvel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dieuwke","family":"Strijker","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cornelis J. 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The trial has been registered in the International Clinical Trials Registry Platform (NL8699). Participants provided written informed consent prior to study participation.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics Approval and Consent to Participate"}},{"value":"Not applicable.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}}]}}