Evidence map›Paper›PMID 25091809›Full record

ArticleStatistical methods in medical research2017

Sample size calculations for prevalent cohort designs.

Hao Liu, Yu Shen, Jing Ning, Jing Qin

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
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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

4 authors.

Hao Liu1 Division of Biostatistics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, USA.
Yu Shen2 Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, USA.
Jing Ning2 Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, USA.
Jing Qin3 Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, USA.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, HELEN E HESLOP · 2007 to 2026
$51.4M
STATISTICAL METHODS FOR BREAST CANCER SCREENING STUDIESR01CA079466 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHEN, YU · 1999 to 2014
$1.5M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA126752NCI NIH HHS R01 CA079466
6 · The paper itself

Abstract

Cross-sectional prevalent cohort design has drawn considerable interests in the studies of association between risk factors and time-to-event outcome. The sampling scheme in such design gives rise to length-biased data that require specialized analysis strategy but can improve study efficiency. The power and sample size calculation methods are however lacking for studies with prevalent cohort design, and using the formula developed for traditional survival data may overestimate sample size. We derive the sample size formulas that are appropriate for the design of cross-sectional prevalent cohort studies, under the assumptions of exponentially distributed event time and uniform follow-up for cross-sectional prevalent cohort design. We perform numerical and simulation studies to compare the sample size requirements for achieving the same power between prevalent cohort and incident cohort designs. We also use a large prospective prevalent cohort study to demonstrate the procedure. Using rigorous designs and proper analysis tools, the prospective prevalent cohort design can be more efficient than the incident cohort design with the same total sample sizes and study durations.

Indexed as

Cohort StudiesResearch DesignBiasCanadaCross-Sectional StudiesDementiaHumansIncidencePrevalenceProspective StudiesSample Sizeincident cohort designlength-biased dataprevalent cohort designsample size determinationsurvival data

Identifiers

PMID25091809
PMCPMC4317376

What OpenQuestion holds

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Registered trials

None linked

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.