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dc.contributor.authorClare, L
dc.contributor.authorHindle, JV
dc.contributor.authorJones, IR
dc.contributor.authorThom, JM
dc.contributor.authorNelis, SM
dc.contributor.authorHounsome, B
dc.contributor.authorWhitaker, CJ
dc.date.accessioned2018-02-20T15:15:40Z
dc.date.issued2012-07-24
dc.description.abstractBACKGROUND: Lifestyle factors playing a role in the development of late-life disability may be modifiable. There is a need for robust evidence about the potential for prevention of disability through behavior change interventions. METHODS/DESIGN: This feasibility study involves the development, implementation and initial testing of a behavior change intervention in a naturalistic setting. A small-scale randomized controlled trial (RCT) will investigate the implementation of a goal-setting intervention aimed at promoting behavior change in the domains of physical and cognitive activity in the context of a community resource center for over-50s. Healthy older participants attending the center (n = 75) will be randomized to one of three conditions: control (an interview involving a general discussion about the center); goal-setting (an interview involving identification of up to five personal goals in the domains of physical activity, cognitive activity, diet and health, and social engagement); or goal-setting with mentoring (the goal-setting interview followed by bi-monthly telephone mentoring). All participants will be reassessed after 12 months. Primary outcomes are levels of physical and cognitive activity. Secondary outcomes address psychosocial (self-efficacy, mood, quality of life), cognitive (memory and executive function), and physical fitness (functional and metabolic) domains. Cost-effectiveness will also be examined. DISCUSSION: This study will provide information about the feasibility of a community-based lifestyle intervention model for over-50s and of the implementation of a goal-setting intervention for behavior change, together with initial evidence about the short-term effects of goal-setting on behavior. TRIAL REGISTRATION: Current Controlled Trials ISRCTN30080637 (http://www.controlled-trials.com).en_GB
dc.description.sponsorshipThis study is funded by the Medical Research Council (UK) through the Lifelong Health and Well-being programme. The funder plays no role in the design of the study, in the collection, analysis and interpretation of data, or in the decision to submit the manuscript for publication. Professors Carol Brayne, Martin Knapp, Mike Martin, and Robin Morris advised on and critically reviewed the study proposal. John Clifford Jones, Maldwyn Roberts, and Stephen Williams of Age Cymru Gwynedd a Môn are responsible for setting up and managing the Nefyn AgeWell Centre. Julie Nixon is conducting the interviews and Jennifer Cooney is contributing to data collection. Anne Krayer will collect and analyze qualitative data for the biographical narrative analysis. Blood samples are analyzed by NHS laboratory staff at Ysbyty Gwynedd, Bangor. Sources of funding for each author are as follows: LC: Higher Education Funding Council for Wales; JVH: National Health Service/ Welsh Assembly Government; IRJ: Higher Education Funding Council for Wales; SMN: Medical Research Council grant; JT: Higher Education Funding Council for Wales; CJW: Welsh Assembly Government.en_GB
dc.identifier.citationVol. 13, pp. 115 - 124en_GB
dc.identifier.doihttps://doi.org/10.1186/1745-6215-13-115
dc.identifier.urihttp://hdl.handle.net/10871/31587
dc.language.isoenen_GB
dc.publisherBioMed Centralen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/22827885en_GB
dc.rights© The Author(s). Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.en_GB
dc.subjectAffecten_GB
dc.subjectAge Factorsen_GB
dc.subjectAgingen_GB
dc.subjectCognitionen_GB
dc.subjectCost-Benefit Analysisen_GB
dc.subjectExecutive Functionen_GB
dc.subjectFeasibility Studiesen_GB
dc.subjectGoalsen_GB
dc.subjectHealth Behavioren_GB
dc.subjectHealth Care Costsen_GB
dc.subjectHealth Promotionen_GB
dc.subjectHealth Statusen_GB
dc.subjectHumansen_GB
dc.subjectLife Styleen_GB
dc.subjectMemoryen_GB
dc.subjectMentorsen_GB
dc.subjectMiddle Ageden_GB
dc.subjectPhysical Fitnessen_GB
dc.subjectQuality of Lifeen_GB
dc.subjectResearch Designen_GB
dc.subjectRisk Reduction Behavioren_GB
dc.subjectSelf Efficacyen_GB
dc.subjectTelephoneen_GB
dc.subjectTime Factorsen_GB
dc.subjectWalesen_GB
dc.titleThe AgeWell study of behavior change to promote health and wellbeing in later life: study protocol for a randomized controlled trial.en_GB
dc.typeArticleen_GB
dc.date.available2018-02-20T15:15:40Z
exeter.place-of-publicationEngland
dc.descriptionThis is the final version of the article. Available from Biomed Central via the DOI in this record.en_GB
dc.identifier.journalTrialsen_GB


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