Evidence map›Paper›PMID 27881108›Full record

Trial reportBMC public health2016

Study protocol for a non-inferiority trial of a blended smoking cessation treatment versus face-to-face treatment (LiveSmokefree-Study).

Lutz Siemer, Marcel E Pieterse, Marjolein G J Brusse-Keizer, Marloes G Postel, Somaya Ben Allouch, Robbert Sanderman

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC public health, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Trial
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  5. The Usability of an Online Tool to Promote the Use of Evidence-Based Smoking Cessation Interventions.International journal of environmental research and public health · 2021
    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

6 authors.

Lutz SiemerResearch Group Technology, Health & Care, Saxion University of Applied Sciences, Postbus 70.000, 7500KB, Enschede, The Netherlands. l.siemer@saxion.nl.ORCID 0000-0003-3019-9113
Marcel E PieterseCentre for eHealth and Well-being Research, University of Twente, Enschede, The Netherlands.
Marjolein G J Brusse-KeizerMedisch Spectrum Twente, Enschede, The Netherlands.
Marloes G PostelCentre for eHealth and Well-being Research, University of Twente, Enschede, The Netherlands.
Somaya Ben AllouchResearch Group Technology, Health & Care, Saxion University of Applied Sciences, Postbus 70.000, 7500KB, Enschede, The Netherlands.
Robbert SandermanCentre for eHealth and Well-being Research, University of Twente, Enschede, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmoking cessation can significantly reduce the risk of developing smoking-related diseases. Several face-to-face and web-based treatments have shown to be effective. Blending of web-based and face-to-face treatment is expected to improve smoking cessation treatment. The primary objective of this study is to compare the prolonged abstinence rate of the blended smoking cessation treatment with the face-to-face treatment. Secondary objectives are to assess the benefits of blended treatment in terms of cost effectiveness and patient satisfaction, and to identify mechanisms underlying successful smoking cessation. METHODS/

designThis study will be a single-center randomized controlled non-inferiority-trial with parallel group design. Patients (n = 344) will be randomly assigned to either the blended or the face-to-face group. Both treatments will consist of ten sessions with equal content held within 6 months. In the blended treatment five out of ten sessions will be delivered online. The treatments will cover the majority of behavior change techniques that are evidence-based within smoking cessation counseling. All face-to-face sessions in both treatments will take place at the outpatient smoking cessation clinic of a hospital. The primary outcome parameter will be biochemically validated prolonged abstinence at 15 months from the start of the smoking cessation treatment. DISCUSSION: This RCT will be the first study to examine the effectiveness of a blended smoking cessation treatment. It will also be the first study to explore patient satisfaction, adherence, cost-effectiveness, and the clinically relevant influencing factors of a blended smoking cessation treatment. The findings of this RCT are expected to substantially strengthen the base of evidence available to inform the development and delivery of smoking cessation treatment.

trial registrationNederlands Trialregister NTR5113 . Registered 24 March 2015.

Indexed as

CounselingSmokingSmoking CessationAdolescentAdultClinical ProtocolsCombined Modality TherapyCost-Benefit AnalysisEquivalence Trials as TopicFemaleHumansInternetMalePatient SatisfactionTime FactorsTreatment OutcomeBlended careBlended treatmenteHealthHealth care sectorInternet-based-treatmentOnline counselingRandomized controlled trialSmoking cessationTobacco use disorder

Identifiers

PMID27881108
PMCPMC5122158

What OpenQuestion holds

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LicenceCC BY
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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.