1. TOPS – a randomized controlled trial of exercise and education to prevent recurrence of low back pain: statistical analysis plan.
- Author
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Ferreira, Giovanni E., Lin, Chung-Wei Christine, Stevens, Matthew Leigh, Hancock, Mark J., Latimer, Jane, Wisbey-Roth, Trish, and Maher, Chris G.
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ACCELEROMETERS , *CHI-squared test , *COMPARATIVE studies , *CONFIDENCE intervals , *COST effectiveness , *EXERCISE therapy , *HEALTH attitudes , *HEALTH surveys , *HOME care services , *MEDICAL care costs , *PATIENT compliance , *PATIENT education , *PATIENT satisfaction , *PHYSICAL therapy , *QUESTIONNAIRES , *RESEARCH funding , *STATISTICAL sampling , *SCALE analysis (Psychology) , *SELF-management (Psychology) , *PAIN management , *STATISTICAL power analysis , *RANDOMIZED controlled trials , *TREATMENT effectiveness , *EDUCATIONAL outcomes , *PROPORTIONAL hazards models , *PHYSICAL activity , *ADVERSE health care events , *DESCRIPTIVE statistics , *LUMBAR pain ,DISEASE relapse prevention - Abstract
• We will monitor compliance with the intervention and adverse events. • Data will be analyzed following intention-to-treat principles. • A cost-effectiveness analysis will be performed. This a priori statistical analysis plan describes the methods of analysis for the Trial Of Prevention Strategies for low back pain (TOPS). TOPS aimed to investigate the effectiveness and cost-effectiveness of exercise and education classes compared with a minimal intervention control in preventing recurrence of low back pain (LBP) in people who have recently recovered from an episode of LBP. TOPS is a superiority, pragmatic, parallel-group randomized controlled trial with allocation concealment, blinded outcome assessors, and intention-to-treat analysis. Participants were randomized to a physical therapist-led exercise and education program for 12 weeks or minimal intervention. The primary outcome was days to recurrence of an episode of LBP. The three key secondary outcomes were days to recurrence of an episode of LBP resulting in (1) activity limitation, (2) care seeking for LBP; and (3) work absence of at least 1 day. Differences in survival curves for the primary (days to recurrence) and secondary outcome (days to LBP with activity limitation, days to care seeking due to LBP, and days to work absence due to LBP) will be compared using Cox regression. Hazard ratios (HRs) and median survival times with 95% confidence intervals (CI) will be calculated. The number of adverse events, including serious adverse events will be reported and the proportion of adverse events between groups will be compared using a Chi-squared test. This paper will provide a detailed description of the planned analyses for the TOPS trial. Australian New Zealand Clinical Trials Registry (ACTRN12615000939594). [ABSTRACT FROM AUTHOR]
- Published
- 2020
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