Evidence map›Paper›PMID 21631623›Full record

Trial reportAddiction (Abingdon, England)2011

Statistical analysis of daily smoking status in smoking cessation clinical trials.

Yimei Li, E Paul Wileyto, Daniel F Heitjan

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Addiction (Abingdon, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Paths to tobacco abstinence: A repeated-measures latent class analysis.Journal of consulting and clinical psychology · 2015
    Trial
  2. Trial
  3. Article
  4. Model-based imputation of latent cigarette counts using data from a calibration study.International journal of methods in psychiatric research · 2016
    Article
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

3 authors.

Yimei LiDivision of Oncology, The Children's Hospital of Philadelphia and Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, PA 19104, USA. liy3@email.chop.edu
E Paul Wileyto
Daniel F Heitjan

Funding

TRANSDISCIPLINARY TOBACCO USE RESEARCH CENTERSP50CA084718 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LERMAN, CARYN · 1999 to 2008
$17.8M
BIOBEHAVIORAL LUNG CANCER PREVENTION PROGRAMR01CA063562 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LERMAN, CARYN · 1993 to 2004
$2.7M
Statistical methods in smoking cessation researchR01CA116723 · NCI · UNIVERSITY OF PENNSYLVANIA · PI HEITJAN, DANIEL FRANCIS · 2007 to 2009
$711k
NCI NIH HHS CA 116723NCI NIH HHS CA 63562NCI NIH HHS CA/DA 84718NCI NIH HHS P50 CA084718NCI NIH HHS R01 CA063562NCI NIH HHS R01 CA116723
6 · The paper itself

Abstract

aimsSmoking cessation trials generally record information on daily smoking behavior, but base analyses on measures of smoking status at the end of treatment (EOT). We present an alternative approach that analyzes the entire sequence of daily smoking status observations.

methodsWe analyzed daily abstinence data from a smoking cessation trial, using two longitudinal logistic regression methods: a mixed-effects (ME) model and a generalized estimating equations (GEE) model. We compared results to a standard analysis that takes abstinence status at EOT as outcome. We evaluated time-varying covariates (smoking history and time-varying drug effect) in the longitudinal analysis and compared ME and GEE approaches.

resultsWe observed some differences in the estimated treatment effect odds ratios across models, with narrower confidence intervals under the longitudinal models. GEE yields similar results to ME when only baseline factors appear in the model, but gives biased results when one includes time-varying covariates. The longitudinal models indicate that the quit probability declines and the drug effect varies over time. Both the previous day's smoking status and recent smoking history predict quit probability, independently of the drug effect.

conclusionWhen analysing outcomes of studies from smoking cessation interventions, longitudinal models with multiple outcome data points, rather than just end of treatment, can makes efficient use of the data and incorporate time-varying covariates. The generalized estimating equations approach should be avoided when using time-varying predictors.

Indexed as

Clinical Trials as TopicModels, StatisticalBupropionData Interpretation, StatisticalDopamine Uptake InhibitorsFemaleHumansMaleOdds RatioOutcome Assessment, Health CareRecurrenceSmokingSmoking CessationTime FactorsBupropionDopamine Uptake Inhibitors

Identifiers

PMID21631623
PMCPMC3197211

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.