Evidence map›Paper›PMID 30400926›Full record

ArticleTrials2018

DELTA

Jonathan A Cook, Steven A Julious, William Sones, Lisa V Hampson, Catherine Hewitt, Jesse A Berlin, Deborah Ashby, Richard Emsley, Dean A Fergusson, Stephen J Walters and 11 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Trials, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04012697 naterminatednot on this mapstarted 2020, after this paper: background citation

A Randomized Controlled Trial of Peer Support Workers in the Emergency Department for People Experiencing Homelessness in the Niagara Region of Ontario, Canada

TypeinterventionalSponsorMcMaster UniversityRan2020 to 2020Enrolled19ConditionsHomelessness, Health Behavior, Health Care Utilization, Health Care Seeking BehaviorArmsPeer Support
NCT06670235 nanot yet recruitingnot on this mapstarted 2024, after this paper: background citation

Effectiveness of Using Upright Versus Lithotomy Birthing Position on Maternal and Newborn Outcomes: A Quasi Experimental Study

TypeinterventionalSponsorHawler Medical UniversityRan2024 to 2026Enrolled124ConditionsMaternal Outcomes, Newborn ComplicationArmsUpright Birthing Position, Lithotomy Birthing Position
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  14. Conceptualizing meaningful between-group difference in change over time: a demonstration of possible viewpoints.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Jonathan A CookCentre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre, Nuffield Orthopaedic Centre, Windmill Rd, Oxford, OX3 7LD, UK. jonathan.cook@ndorms.ox.ac.uk.ORCID http://orcid.org/0000-0002-4156-6989
Steven A JuliousMedical Statistics Group, ScHARR, The University of Sheffield, Regent Court, 30 Regent Street, Sheffield, S1 4DA, UK.
William SonesCentre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre, Nuffield Orthopaedic Centre, Windmill Rd, Oxford, OX3 7LD, UK.
Lisa V HampsonStatistical Methodology and Consulting, Novartis, Basel, Switzerland.
Catherine HewittDepartment of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, York, YO10 5DD, UK.
Jesse A BerlinJohnson & Johnson, 1125 Trenton-Harbourton Road, Titusville, NJ, 08933, USA.
Deborah AshbyImperial Clinical Trials Unit, School of Public Health, Imperial College London, Stadium House, 68 Wood Lane, London, W12 7RH, UK.
Richard EmsleyDepartment of Biostatistics and Health Informatics, Institute of Psychiatry, Psychology and Neuroscience, King's College London, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
Dean A FergussonClinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Stephen J WaltersMedical Statistics Group, ScHARR, The University of Sheffield, Regent Court, 30 Regent Street, Sheffield, S1 4DA, UK.
Edward C F WilsonCambridge Centre for Health Services Research & Cambridge Clinical Trials Unit, University of Cambridge, Institute of Public Health, Forvie Site, Robinson Way, Cambridge, CB2 0SR, UK.
Graeme MaclennanThe Centre for Healthcare Randomised Trials (CHaRT), Health Sciences Building, University of Aberdeen, Foresterhill, Aberdeen, AB25 2D, UK.
Nigel StallardWarwick Medical School - Statistics and Epidemiology, University of Warwick, Coventry, CV4 7AL, UK.
Joanne C RothwellMedical Statistics Group, ScHARR, The University of Sheffield, Regent Court, 30 Regent Street, Sheffield, S1 4DA, UK.
Martin BlandDepartment of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, York, YO10 5DD, UK.
Louise BrownMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, 2nd Floor 90 High Holborn, London, WC1V 6LJ, UK.
Craig R RamsayHealth Services Research Unit, University of Aberdeen, Health Sciences Building Foresterhill, Aberdeen, AB25 2ZD, UK.
Andrew CookPublic Health Medicine and Fellow in Health Technology Assessment, Wessex Institute, University of Southampton, Alpha House, Enterprise Road, Southampton, SO16 7NS, UK.
David ArmstrongSchool of Population Health & Environmental Sciences, Faculty of Life Sciences and Medicine, Kings College London, Addison House, Guy's Campus, London, SE1 1UL, UK.
Doug AltmanCentre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre, Nuffield Orthopaedic Centre, Windmill Rd, Oxford, OX3 7LD, UK.
Luke D ValeHealth Economics Group, Institute of Health & Society, Newcastle University, Newcastle upon Tyne, NE2 4AX, UK.

Funding

Chief Scientist Office HSRU1Medical Research Council MC_PC_16101Medical Research Council MC_UU_12023/29Medical Research Council N/ANational Institute for Health Research N/A
6 · The paper itself

Abstract

backgroundA key step in the design of a RCT is the estimation of the number of participants needed in the study. The most common approach is to specify a target difference between the treatments for the primary outcome and then calculate the required sample size. The sample size is chosen to ensure that the trial will have a high probability (adequate statistical power) of detecting a target difference between the treatments should one exist. The sample size has many implications for the conduct and interpretation of the study. Despite the critical role that the target difference has in the design of a RCT, the way in which it is determined has received little attention. In this article, we summarise the key considerations and messages from new guidance for researchers and funders on specifying the target difference, and undertaking and reporting a RCT sample size calculation. This article on choosing the target difference for a randomised controlled trial (RCT) and undertaking and reporting the sample size calculation has been dual published in the BMJ and BMC Trials journals

methodsThe DELTA RESULTS AND DISCUSSION: The key messages from the DELTA

Indexed as

Randomized Controlled Trials as TopicSample SizeDelphi TechniqueGuidelines as TopicHumansNumbers Needed To TreatResearch Report

Identifiers

PMID30400926
PMCPMC6218987

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.