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      Effects of a remotely supervised physical training program combined with cognitive training for older individuals at increased risk of clinical-functional vulnerability: study protocol for a randomized clinical trial

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          Abstract

          Background

          Despite the robust body of evidence for the benefits of home-based physical exercise, there is still a paucity of data on the benefits of home-based cognitive training for older adults, especially in those at increased risk of clinical-functional vulnerability. As such, the present study aims to compare the chronic effects of a telehealth-delivered physical training intervention alone or combined with a cognitive training program in older adults at increased clinical-functional vulnerability risk.

          Methods

          A randomized clinical trial will be conducted including 62 sedentary older individuals classified as at increased risk of clinical-functional vulnerability based on their Clinical-Functional Vulnerability Index score. Participants will be randomly allocated in a 1:1 ratio to one of two groups, an intervention group including physical training combined with cognitive training, or an active control group including physical training alone. Both groups will receive home-based supervised training remotely for 12 weeks and will be assessed for the primary and secondary outcomes of the study before and after the training period. Primary outcomes include cognitive function and dynamic balance with a dual task. Secondary outcomes encompass physical, cognitive, and occupational performance, functional capacity, quality of life, and anxiety and depression symptoms, as well as hemodynamic measures. Data analysis will be performed by intention-to-treat and per protocol using mixed linear models and Bonferroni’s post hoc ( α = 0.05).

          Discussion

          Our conceptual hypothesis is that both groups will show improvements in the primary and secondary outcomes. Nevertheless, we expect physical combined with cognitive training to improve cognitive function, dual task, and occupational performance to a greater degree as compared to physical training alone.

          Trial registration

          NCT05309278. Registered on April 4, 2022.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s13063-023-07567-8.

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          Most cited references53

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          The hospital anxiety and depression scale.

          A self-assessment scale has been developed and found to be a reliable instrument for detecting states of depression and anxiety in the setting of an hospital medical outpatient clinic. The anxiety and depressive subscales are also valid measures of severity of the emotional disorder. It is suggested that the introduction of the scales into general hospital practice would facilitate the large task of detection and management of emotional disorder in patients under investigation and treatment in medical and surgical departments.
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            SPIRIT 2013 statement: defining standard protocol items for clinical trials.

            The protocol of a clinical trial serves as the foundation for study planning, conduct, reporting, and appraisal. However, trial protocols and existing protocol guidelines vary greatly in content and quality. This article describes the systematic development and scope of SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) 2013, a guideline for the minimum content of a clinical trial protocol.The 33-item SPIRIT checklist applies to protocols for all clinical trials and focuses on content rather than format. The checklist recommends a full description of what is planned; it does not prescribe how to design or conduct a trial. By providing guidance for key content, the SPIRIT recommendations aim to facilitate the drafting of high-quality protocols. Adherence to SPIRIT would also enhance the transparency and completeness of trial protocols for the benefit of investigators, trial participants, patients, sponsors, funders, research ethics committees or institutional review boards, peer reviewers, journals, trial registries, policymakers, regulators, and other key stakeholders.
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              2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults

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                Author and article information

                Contributors
                franberni2@gmail.com
                ana_kanitz@yahoo.com.br
                camilamiranda1313@gmail.com
                denerbudziarek@hotmail.com
                marco.bergamin@unipd.it
                valentina.bullo@unipd.it
                gustavo.schaun@univie.ac.at
                cristine.alberton@ufpel.edu.br
                Journal
                Trials
                Trials
                Trials
                BioMed Central (London )
                1745-6215
                21 August 2023
                21 August 2023
                2023
                : 24
                : 547
                Affiliations
                [1 ]GRID grid.411221.5, ISNI 0000 0001 2134 6519, Physical Education School, , Universidade Federal de Pelotas, ; Pelotas, RS Brazil
                [2 ]GRID grid.8532.c, ISNI 0000 0001 2200 7498, School of Physical Education, Physical Therapy and Dance, , Universidade Federal Do Rio Grande Do Sul, ; Porto Alegre, RS Brazil
                [3 ]GRID grid.5608.b, ISNI 0000 0004 1757 3470, Department of Medicine, , University of Padova, ; Padua, Italy
                [4 ]GRID grid.10420.37, ISNI 0000 0001 2286 1424, Centre for Sport Science and University Sports, , University of Vienna, ; Vienna, Austria
                Author information
                http://orcid.org/0000-0003-3339-714X
                Article
                7567
                10.1186/s13063-023-07567-8
                10440879
                37599360
                3c4ac22e-5356-4af1-a497-ed49e29393ff
                © BioMed Central Ltd., part of Springer Nature 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, 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 changes were made. 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/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 2 June 2023
                : 4 August 2023
                Funding
                Funded by: University of Vienna
                Categories
                Study Protocol
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Medicine
                exercise,physical training,cognitive training,tele-rehabilitation,elderly
                Medicine
                exercise, physical training, cognitive training, tele-rehabilitation, elderly

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