dc.contributor.author
Guerra Balic, Miriam
dc.contributor.author
Montané Mogas, Joel
dc.contributor.author
Dardashtipour, Elnaz
dc.contributor.author
Canivell Fusté, Silvia
dc.contributor.author
Azarbayjani, Mohammad Ali
dc.contributor.author
Fuente Vidal, Andrea
dc.contributor.author
Surroca, Aina
dc.contributor.author
Gascón Lecha, M. Pilar
dc.contributor.author
Mestres Miralles, Concepción
dc.contributor.author
Antón, Alicia
dc.contributor.author
Peña-Mateo, Maria José
dc.contributor.author
Carrillo-Alvarez, Elena
dc.contributor.author
Canudas Teixidó, Anna-Maria
dc.date.accessioned
2026-01-28T13:05:57Z
dc.date.available
2026-01-28T13:05:57Z
dc.date.issued
2026-01-27T09:50:18Z
dc.date.issued
2026-01-27T09:50:18Z
dc.date.issued
2026-01-05
dc.date.issued
2026-01-27T09:50:18Z
dc.identifier
https://hdl.handle.net/2445/226215
dc.identifier.uri
http://hdl.handle.net/2445/226215
dc.description.abstract
Introduction: Aerobic and resistance training can effectively improve clinicalmanagement in people with type 2 diabetes (T2D). Low vitamin D (VitD) levels areassociated with T2D risk and metabolic disturbances, and may help reduce thisrisk, particularly in individuals with low VitD levels. In this line, many individualswith T2D, who may also be older adults or have osteoporosis, regularly includeVitD treatment in their healthcare routines. Although the impact of exercisehas been extensively studied, its effect on diabetic patients taking VitD remainslimited. The aim of this study is to investigate the effect of aerobic and resistancetraining on clinical parameters in patients with T2D already taking VitD.Methods: The DIAVITEX study is a randomized controlled superiority trial, withfour parallel arms, including 80 individuals with T2D. Patients will be selectedat the Primary Care Centers and stratified according to their pre-existingVitD treatment. Participants will subsequently be randomized to the exerciseintervention or control as follows: Group 1, Exercise + VitD users (n = 20);Group 2, Exercise + VitD non-users (n = 20); Group 3, VitD only (no exercise)(n = 20); and Group 4, Control (No VitD & No Exercise) (n = 20). In this study,a sarcoplasm-stimulating training program will be carried out online, threesessions per week for a total of 16 weeks. Before and after the physical activitysubjects will perform fitness and blood tests. Nutritional education programswill be provided to normalize their diets for study consistency. The primaryendpoint of the trial is the change in HOMA-IR index from baseline to week 16.Secondary endpoints include changes in HbA1c, lipid profile, body composition,and inflammatory biomarkers.Discussion: Expected improvements in insulin resistance, glycated hemoglobin,lipid profile, and inflammatory markers are anticipated following a 16-weekregimen of exercise in patients with T2D on VitD.Clinical trial registration: The study was registered on September 21, 2024,with the identifier number NCT06081387, https://clinicaltrials.gov/study/NCT06081387.
dc.format
application/pdf
dc.publisher
Frontiers Media
dc.relation
Reproducció del document publicat a: https://doi.org/10.3389/fpubh.2025.1674293
dc.relation
Frontiers In Public Health, 2026
dc.relation
https://doi.org/10.3389/fpubh.2025.1674293
dc.rights
cc-by (c) Dardashtipour, E. et al., 2026
dc.rights
http://creativecommons.org/licenses/by/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.title
The effect of aerobic and resistance training in patientswith type 2 diabetes on vitamin D(DIAVITEX): a study protocol
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion