Influence of trial sample size on treatment effect estimates: meta-epidemiological study

A Dechartres, L Trinquart, I Boutron, P Ravaud - Bmj, 2013 - bmj.com
Objective To assess the influence of trial sample size on treatment effect estimates within
meta-analyses. Design Meta-epidemiological study. Data sources 93 meta-analyses (735 …

Assessing the generalizability of randomized trial results to target populations

EA Stuart, CP Bradshaw, PJ Leaf - Prevention Science, 2015 - Springer
Recent years have seen increasing interest in and attention to evidence-based practices,
where the “evidence” generally comes from well-conducted randomized trials. However …

AHRQ series paper 1: comparing medical interventions: AHRQ and the effective health-care program

J Slutsky, D Atkins, S Chang, BAC Sharp - Journal of clinical epidemiology, 2010 - Elsevier
In 2005, the Agency for Healthcare Research and Quality established the Effective Health
Care (EHC) Program. The EHC Program aims to provide understandable and actionable …

Practical clinical trials for translating research to practice: design and measurement recommendations

RE Glasgow, DJ Magid, A Beck, D Ritzwoller… - Medical care, 2005 - journals.lww.com
Objective: The objective of this study was to build on the seminal paper by Tunis et al
(Practical clinical trials. Increasing the value of clinical research for decision making in …

Why observational studies should be among the tools used in comparative effectiveness research

NA Dreyer, SR Tunis, M Berger, D Ollendorf… - Health …, 2010 - healthaffairs.org
Doctors, patients, and other decision makers need access to the best available clinical
evidence, which can come from systematic reviews, experimental trials, and observational …

[HTML][HTML] Different ways to estimate treatment effects in randomised controlled trials

J Twisk, L Bosman, T Hoekstra, J Rijnhart… - Contemporary clinical …, 2018 - Elsevier
Background Regarding the analysis of RCT data there is a debate going on whether an
adjustment for the baseline value of the outcome variable should be made. When an …

Alternatives to randomisation in the evaluation of public-health interventions: statistical analysis and causal inference

S Cousens, J Hargreaves, C Bonell… - … of Epidemiology & …, 2011 - jech.bmj.com
Background In non-randomised evaluations of public-health interventions, statistical
methods to control confounding will usually be required. We review approaches to the …

Quasi-experimental study designs series—paper 6: risk of bias assessment

H Waddington, AM Aloe, BJ Becker, EW Djimeu… - Journal of Clinical …, 2017 - Elsevier
Objectives Rigorous and transparent bias assessment is a core component of high-quality
systematic reviews. We assess modifications to existing risk of bias approaches to …

An audit of sample sizes for pilot and feasibility trials being undertaken in the United Kingdom registered in the United Kingdom Clinical Research Network database

SAM Billingham, AL Whitehead, SA Julious - BMC medical research …, 2013 - Springer
Background There is little published guidance as to the sample size required for a pilot or
feasibility trial despite the fact that a sample size justification is a key element in the design …

Recruitment and retention of participants in randomised controlled trials: a review of trials funded and published by the United Kingdom Health Technology …

SJ Walters, IB dos Anjos Henriques-Cadby… - BMJ open, 2017 - bmjopen.bmj.com
Background Substantial amounts of public funds are invested in health research worldwide.
Publicly funded randomised controlled trials (RCTs) often recruit participants at a slower …