Publication:
EVIDENT 3 Study: A randomized, controlled clinical trial to reduce inactivity and caloric intake in sedentary and overweight or obese people using a smartphone application Study protocol

dc.contributor.authorRecio-Rodriguez, Jose I
dc.contributor.authorGomez-Marcos, Manuel A
dc.contributor.authorAgudo-Conde, Cristina
dc.contributor.authorRamirez, Ignasi
dc.contributor.authorGonzalez-Viejo, Natividad
dc.contributor.authorGomez-Arranz, Amparo
dc.contributor.authorSalcedo-Aguilar, Fernando
dc.contributor.authorRodriguez-Sanchez, Emiliano
dc.contributor.authorAlonso-Dominguez, Rosario
dc.contributor.authorSanchez-Aguadero, Natalia
dc.contributor.authorGonzalez-Sanchez, Jesus
dc.contributor.authorGarcia-Ortiz, Luis
dc.contributor.authorEVIDENT 3 Investigators
dc.date.accessioned2024-09-06T09:55:57Z
dc.date.available2024-09-06T09:55:57Z
dc.date.issued2018-01
dc.description.abstractIntroduction: Mobile technology, when included within multicomponent interventions, could contribute to more effective weight loss. The objective of this project is to assess the impact of adding the use of the EVIDENT 3 application, designed to promote healthy living habits, to traditional modification strategies employed for weight loss. Other targeted behaviors (walking, caloric-intake, sitting time) and outcomes (quality of life, inflammatory markers, measurements of arterial aging) will also be evaluated. Methods: Randomized, multicentre clinical trial with 2 parallel groups. The study will be conducted in the primary care setting and will include 700 subjects 20 to 65 years, with a body mass index (27.5-40kg/m(2)), who are clinically classified as sedentary. The primary outcome will be weight loss. Secondary outcomes will include change in walking (steps/d), sitting time (min/wk), caloric intake (kcal/d), quality of life, arterial aging (augmentation index), and pro-inflammatory marker levels. Outcomes will be measured at baseline, after 3 months, and after 1 year. Participants will be randomly assigned to either the intervention group (IG) or the control group (CG). Both groups will receive the traditional primary care lifestyle counseling prior to randomization. The subjects in the IG will be lent a smartphone and a smartband for a 3-month period, corresponding to the length of the intervention. The EVIDENT 3 application integrates the information collected by the smartband on physical activity and the self-reported information by participants on daily food intake. Using this information, the application generates recommendations and personalized goals for weight loss. Discussion: There is a great diversity in the applications used obtaining different results on lifestyle improvement and weight loss. The populations studied are not homogeneous and generate different results. The results of this study will help our understanding of the efficacy of new technologies, combined with traditional counseling, towards reducing obesity and enabling healthier lifestyles. Ethicsanddissemination: The study was approved by the Clinical Research Ethics Committee of the Health Area of Salamanca (CREC of Health Area of Salamanca) on April 2016. A SPIRIT checklist is available for this protocol.en
dc.description.sponsorshipThis study was supported in part by grants funded by the Spanish Ministry of Science and Innovation (MICINN) and Instituto de Salud Carlos III/European Regional Development Fund (ERDF) (RD12/0005/0001, RD16/0007/0003, RD16/0007/0005, RD16/0007/0008, RD16/0007/0009) and (PI16/00101, PI16/00952, PI16/00765, PI16/00659, PI16/00421, PI16/00170). Gerencia Regional de Salud de Castilla y Leon (GRS 1277/B/16) also collaborated in the funding of this study.es_ES
dc.format.number2es_ES
dc.format.pagee9633es_ES
dc.format.volume97es_ES
dc.identifier.citationRecio-Rodriguez JI, Gomez-Marcos MA, Agudo-Conde C, Ramírez Manent JI, Gonzalez-Viejo N, Gomez-Arranz A, et al. EVIDENT 3 Study: A randomized, controlled clinical trial to reduce inactivity and caloric intake in sedentary and overweight or obese people using a smartphone application Study protocol. Medicine (Baltimore). 2018 Jan;97(2):e9633.en
dc.identifier.doi10.1097/MD.0000000000009633
dc.identifier.e-issn1536-5964es_ES
dc.identifier.issn0025-7974
dc.identifier.journalMedicinees_ES
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/9447
dc.identifier.pubmedID29480874es_ES
dc.identifier.puiL620566137
dc.identifier.scopus2-s2.0-85041458307
dc.identifier.urihttps://hdl.handle.net/20.500.12105/22572
dc.identifier.wos424081000054
dc.language.isoengen
dc.publisherLippincott Williams & Wilkins (LWW)
dc.relation.publisherversionhttps://dx.doi.org/10.1097/MD.0000000000009633en
dc.rights.accessRightsopen accessen
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectArterial aging
dc.subjectFood
dc.subjectmHealth
dc.subjectObesity
dc.subjectPhysical activity
dc.subjectWeight loss
dc.subject.decsPérdida de Peso*
dc.subject.decsEjercicio Físico*
dc.subject.decsResultado del Tratamiento*
dc.subject.decsConductas Relacionadas con la Salud*
dc.subject.decsAplicaciones Móviles*
dc.subject.decsRestricción Calórica*
dc.subject.decsConsejo*
dc.subject.decsHumanos*
dc.subject.decsPersona de Mediana Edad*
dc.subject.decsCalidad de Vida*
dc.subject.decsTeléfono Inteligente*
dc.subject.decsAdulto Joven*
dc.subject.decsEstilo de Vida*
dc.subject.decsAnciano*
dc.subject.decsAdulto*
dc.subject.decsSobrepeso*
dc.subject.meshAged*
dc.subject.meshYoung Adult*
dc.subject.meshAdult*
dc.subject.meshSmartphone*
dc.subject.meshHumans*
dc.subject.meshLife Style*
dc.subject.meshMiddle Aged*
dc.subject.meshMobile Applications*
dc.subject.meshCounseling*
dc.subject.meshHealth Behavior*
dc.subject.meshQuality of Life*
dc.subject.meshTreatment Outcome*
dc.subject.meshWeight Loss*
dc.subject.meshCaloric Restriction*
dc.subject.meshOverweight*
dc.subject.meshExercise*
dc.titleEVIDENT 3 Study: A randomized, controlled clinical trial to reduce inactivity and caloric intake in sedentary and overweight or obese people using a smartphone application Study protocolen
dc.typeresearch articleen
dspace.entity.typePublication
relation.isPublisherOfPublicationf94ef1f2-f26f-4ebc-84d7-bb83b401e22a
relation.isPublisherOfPublication.latestForDiscoveryf94ef1f2-f26f-4ebc-84d7-bb83b401e22a

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