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Effectiveness of a Healthy Lifestyle Program (HeLP) for low back pain: statistical analysis plan for a randomised controlled trial.
Robson, Emma; Kamper, Steven J; Hall, Alix; Lee, Hopin; Davidson, Simon; da Silva, Priscilla Viana; Gleadhill, Connor; Williams, Christopher M.
Afiliación
  • Robson E; School of Medicine and Public Health, University of Newcastle, Callaghan, NSW, Australia.
  • Kamper SJ; Hunter New England Population Health, Wallsend, NSW, Australia.
  • Hall A; School of Health Sciences, University of Sydney, Camperdown, NSW, Australia.
  • Lee H; Nepean Blue Mountains Local Health District, Penrith, NSW, Australia.
  • Davidson S; School of Medicine and Public Health, University of Newcastle, Callaghan, NSW, Australia.
  • da Silva PV; Hunter New England Population Health, Wallsend, NSW, Australia.
  • Gleadhill C; School of Medicine and Public Health, University of Newcastle, Callaghan, NSW, Australia.
  • Williams CM; Hunter New England Population Health, Wallsend, NSW, Australia.
Trials ; 22(1): 648, 2021 Sep 22.
Article en En | MEDLINE | ID: mdl-34551809
ABSTRACT

BACKGROUND:

This paper describes the statistical analysis plan for a randomised controlled trial of a Healthy Lifestyle Program (HeLP) for low back pain targeting multiple health risks and behaviours, weight, physical activity, diet and smoking, to improve disability. We describe the methods for the main analyses and economic analysis of the trial. METHODS AND

DESIGN:

The trial is a two-arm pragmatic randomised controlled trial comparing the effect of the HeLP intervention to usual care on low back pain disability at 26 weeks. A total of 346 adults with low back pain were recruited from the Newcastle and Hunter region between September 2017 and November 2019 and randomised to either HeLP or usual care. HeLP is a 6-month intervention with participant outcomes measured at weeks 6, 12, 26 and 52 post randomisation. This statistical analysis plan describes data integrity, handling and preparation of data for analyses and methods for analyses. The primary endpoint for the trial is disability at 26 weeks using the 24-item self-report Roland Morris Disability Questionnaire. The primary analysis will follow the intention-to-treat principle using linear mixed regression models.

DISCUSSION:

The statistical analysis plan for this trial was produced to reduce outcome reporting bias arising from knowledge of the study findings. Any deviations will be described and justified in the final report. TRIAL REGISTRATION Australian New Zealand Clinical Trials Registry ACTRN12617001288314 . Registered on 6 September 2017.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dolor de la Región Lumbar Tipo de estudio: Clinical_trials / Diagnostic_studies / Evaluation_studies / Prognostic_studies Límite: Adult / Humans País/Región como asunto: Oceania Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2021 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dolor de la Región Lumbar Tipo de estudio: Clinical_trials / Diagnostic_studies / Evaluation_studies / Prognostic_studies Límite: Adult / Humans País/Región como asunto: Oceania Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2021 Tipo del documento: Article País de afiliación: Australia