dc.contributor.author
Martín Borràs, Carme
dc.contributor.author
Giné-Garriga, Maria
dc.contributor.author
Martínez Ramos, Elena
dc.contributor.author
Martín Cantera, Carlos
dc.contributor.author
Puigdoménech, Elisa
dc.contributor.author
Solà Gonfaus, Mercè
dc.contributor.author
Castillo Ramos, Eva
dc.contributor.author
Beltrán, Angela Mª
dc.contributor.author
Puig Ribera, Anna
dc.contributor.author
Trujillo, José Manuel
dc.contributor.author
Pueyo, Olga
dc.contributor.author
Pueyo, Javier
dc.contributor.author
Rodríguez, Beatriz
dc.contributor.author
Serra Payà, Noemí
dc.date.accessioned
2024-12-05T21:22:20Z
dc.date.available
2024-12-05T21:22:20Z
dc.date.issued
2018-11-15T08:26:55Z
dc.date.issued
2018-11-15T08:26:55Z
dc.identifier
https://doi.org/10.1186/1471-2458-14-228
dc.identifier
http://hdl.handle.net/10459.1/65107
dc.identifier.uri
http://hdl.handle.net/10459.1/65107
dc.description.abstract
Background
There is growing evidence suggesting that prolonged sitting has negative effects on people’s weight, chronic diseases and mortality. Interventions to reduce sedentary time can be an effective strategy to increase daily energy expenditure. The purpose of this study is to evaluate the effectiveness of a six-month primary care intervention to reduce daily of sitting time in overweight and mild obese sedentary patients.
Method/Design
The study is a randomized controlled trial (RCT). Professionals from thirteen primary health care centers (PHC) will randomly invite to participate mild obese or overweight patients of both gender, aged between 25 and 65 years old, who spend 6 hours at least daily sitting. A total of 232 subjects will be randomly allocated to an intervention (IG) and control group (CG) (116 individuals each group). In addition, 50 subjects with fibromyalgia will be included.
Primary outcome is: (1) sitting time using the activPAL device and the Marshall questionnaire. The following parameters will be also assessed: (2) sitting time in work place (Occupational Sitting and Physical Activity Questionnaire), (3) health-related quality of life (EQ-5D), (4) evolution of stage of change (Prochaska and DiClemente's Stages of Change Model), (5) physical inactivity (catalan version of Brief Physical Activity Assessment Tool), (6) number of steps walked (pedometer and activPAL), (7) control based on analysis (triglycerides, total cholesterol, HDL, LDL, glycemia and, glycated haemoglobin in diabetic patients) and (8) blood pressure and anthropometric variables. All parameters will be assessed pre and post intervention and there will be a follow up three, six and twelve months after the intervention. A descriptive analysis of all variables and a multivariate analysis to assess differences among groups will be undertaken. Multivariate analysis will be carried out to assess time changes of dependent variables. All the analysis will be done under the intention to treat principle.
Discussion
If the SEDESTACTIV intervention shows its effectiveness in reducing sitting time, health professionals would have a low-cost intervention tool for sedentary overweight and obese patients management.
dc.description.abstract
Funding was received from the Instituto de Salud Carlos III (PI11/01082) for the development of the randomized controlled trial. Also from the Barcelona Primary Health Care Research Unit, Institut Català de la Salut (Ajut XB) to develop an observational SEDESTACTIV study.
dc.publisher
BioMed Central
dc.relation
Reproducció del document publicat a https://doi.org/10.1186/1471-2458-14-228
dc.relation
BMC Public Health, 2014, vol. 14, art. 228
dc.rights
cc-by (c) C. Martín-Borràs et al., 2014
dc.rights
info:eu-repo/semantics/openAccess
dc.rights
http://creativecommons.org/licenses/by/4.0/
dc.subject
Sedentary behaviour
dc.title
Effectiveness of a primary care-based intervention to reduce sitting time in overweight and obese patients (SEDESTACTIV): a randomized controlled trial; rationale and study design
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion