نتایج جستجو برای: sample size calculation

تعداد نتایج: 994380  

Journal: :Lancet 2005
Kenneth F Schulz David A Grimes

Investigators should properly calculate sample sizes before the start of their randomised trials and adequately describe the details in their published report. In these a-priori calculations, determining the effect size to detect--eg, event rates in treatment and control groups--reflects inherently subjective clinical judgments. Furthermore, these judgments greatly affect sample size calculatio...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2012
Jae Kwan Jun Mi Jin Kim Kui Son Choi Mina Suh Kyu-Won Jung

Mammographic breast density is a known risk factor for breast cancer. To conduct a survey to estimate the distribution of mammographic breast density in Korean women, appropriate sampling strategies for representative and efficient sampling design were evaluated through simulation. Using the target population from the National Cancer Screening Programme (NCSP) for breast cancer in 2009, we veri...

2013
Ashley Jones Elizabeth Conroy Paula Williamson Mike Clarke Carrol Gamble

BACKGROUND A systematic review, with or without a meta-analysis, should be undertaken to determine if the research question of interest has already been answered before a new trial begins. There has been limited research on how systematic reviews are used within the design of new trials, the aims of this study were to investigate how systematic reviews of earlier trials are used in the planning...

2017
K. J. Wareham R. M. Hyde D. Grindlay M. L. Brennan R. S. Dean

BACKGROUND Randomised controlled trials (RCTs) are a key component of the veterinary evidence base. Sample sizes and defined outcome measures are crucial components of RCTs. To describe the sample size and number of outcome measures of veterinary RCTs either funded by the pharmaceutical industry or not, published in 2011. METHODS A structured search of PubMed identified RCTs examining the eff...

2013
Richard Hooper

Background The ethical significance of sample size is enshrined in principles of Good Clinical Practice and in quality standards for reporting trial results, yet sample size is often one of the most ill-considered aspects of a grant application. Researchers are also battling with an increasing complexity in study design. With some adaptive trial designs, for example, analytical solutions to sam...

Journal: :International Journal of Ayurveda Research 2010

Journal: :gastroenterology and hepatology from bed to bench 0
mohamad amin pourhoseingholi department of biostatistics, shahid beheshti university of medical sciences, tehran, iran mohsen vahedi department of epidemiology and biostatistics, school of public health, tehran university of medical sciences, tehran, iran mitra rahimzadeh

optimum sample size is an essential component of any research. the main purpose of the sample size calculation is to determine the enough number of units needed to detect the unknown clinical parameters or the treatment effects or the association after data gathering. it is not uncommon for studies to be underpowered and failing to detect the existed treatment effects due to inadequate sample s...

2014
Jacqueline J Hill Willem Kuyken David A Richards

BACKGROUND Stepped care is recommended and implemented as a means to organise depression treatment. Compared with alternative systems, it is assumed to achieve equivalent clinical effects and greater efficiency. However, no trials have examined these assumptions. A fully powered trial of stepped care compared with intensive psychological therapy is required but a number of methodological and pr...

Journal: :Health technology assessment 2014
Jonathan A Cook Jennifer Hislop Temitope E Adewuyi Kirsten Harrild Douglas G Altman Craig R Ramsay Cynthia Fraser Brian Buckley Peter Fayers Ian Harvey Andrew H Briggs John D Norrie Dean Fergusson Ian Ford Luke D Vale

BACKGROUND The randomised controlled trial (RCT) is widely considered to be the gold standard study for comparing the effectiveness of health interventions. Central to the design and validity of a RCT is a calculation of the number of participants needed (the sample size). The value used to determine the sample size can be considered the 'target difference'. From both a scientific and an ethica...

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