Evidence map›Paper›PMID 22525000›Full record

Trial reportAlcoholism, clinical and experimental research2012

Trajectory analyses in alcohol treatment research.

Jinsong Chen, Bankole A Johnson, Xin-Qun Wang, John O'Quigley, Maria Isaac, Daowen Zhang, Lei Liu

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Alcoholism, clinical and experimental research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

7 authors at 4 institutions in 2 countries.

Jinsong ChenDepartment of Preventive Medicine, Northwestern University, Chicago, Illinois, USA.
Bankole A Johnson
Xin-Qun Wang
John O'Quigley
Maria Isaac
Daowen Zhang
Lei Liu
University of Virginia · USNorthwestern University · USInstitute of Family Therapy · GBNorth Carolina State University · US

Funding

Statistical Methods for AIDS Clinical TrialsR37AI031789 · NIAID · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TSIATIS, ANASTASIOS A · 2003 to 2012
$3.2M
Flexible Statistical Methods for Biomedical DataR01CA085848 · NCI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI DAVIDIAN, MARIE · 2000 to 2015
$3.1M
Innovative methods for modeling longitudianl medical costsR01HS020263 · AHRQ · UNIVERSITY OF VIRGINIA · PI LIU, LEI · 2011 to 2015
$2.0M
Genome-wide Haplotype Association Analysis in Mental DisordersR01MH084022 · NIMH · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TZENG, JUNG-YING · 2009 to 2011
$1.1M
Innovative Analytic Methods of Person-Centered Data and Adaptive Designs for AlcoRC1AA019274 · NIAAA · UNIVERSITY OF VIRGINIA · PI JOHNSON, BANKOLE A, LIU, LEI · 2009 to 2010
$671k
AHRQ HHS R01 HS020263NCI NIH HHS R01 CA085848NCI NIH HHS R01 CA085848-11NIAAA NIH HHS RC1 AA019274NIAAA NIH HHS RC1AA019274NIAID NIH HHS R37 AI031789NIAID NIH HHS R37 AI031789-20NIMH NIH HHS R01 MH084022NIMH NIH HHS R01 MH084022-02
6 · The paper itself

Abstract

backgroundVarious statistical methods have been used for data analysis in alcohol treatment studies. Trajectory analyses can better capture differences in treatment effects and may provide insight on the optimal duration of future clinical trials and grace periods. This improves on the limitation of commonly used parametric (e.g., linear) methods that cannot capture nonlinear temporal trends in the data.

methodsWe propose an exploratory approach, using more flexible smoothing mixed effects models, more accurately to characterize the temporal patterns of the drinking data. We estimated the trajectories of the treatment arms for data sets from 2 sources: a multisite topiramate study, and the Combined Pharmacotherapies (acamprosate and naltrexone) and Behavioral Interventions study.

resultsOur methods illustrate that drinking outcomes of both the topiramate and placebo arms declined over the entire course of the trial but with a greater rate of decline for the topiramate arm. By the point-wise confidence intervals, the heavy drinking probabilities for the topiramate arm might differ from those of the placebo arm as early as week 2. Furthermore, the heavy drinking probabilities of both arms seemed to stabilize at the end of the study. Overall, naltrexone was better than placebo in reducing drinking over time yet was not different from placebo for subjects receiving the combination of a brief medical management and an intensive combined behavioral intervention.

conclusionsThe estimated trajectory plots clearly showed nonlinear temporal trends of the treatment with different medications on drinking outcomes and offered more detailed interpretation of the results. This trajectory analysis approach is proposed as a valid exploratory method for evaluating efficacy in pharmacotherapy trials in alcoholism.

Indexed as

AcamprosateAdultAgedAged, 80 and overAlcohol DeterrentsAlcoholismAlgorithmsBehavior TherapyCombined Modality TherapyData Interpretation, StatisticalDouble-Blind MethodFemaleFructoseHumansLinear ModelsMaleAcamprosateAlcohol DeterrentsFructoseNaltrexoneNarcotic AntagonistsNeuroprotective AgentsTaurineTopiramate

Identifiers

PMID22525000
PMCPMC3407320
OpenAlexW2154252461

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.