Evidence map›Paper›PMID 38184633›Full record

ArticleTrials2024

Update of statistical analysis plan for: Integration of smoking cessation into standard treatment for patients receiving opioid agonist therapy who are smoking tobacco: protocol for a randomised controlled trial (ATLAS4LAR).

Karl Trygve Druckrey-Fiskaaen, Tesfaye Madebo, Jan Tore Daltveit, Jørn Henrik Vold, Einar Furulund, Torgeir Gilje Lid, Lars Thore Fadnes

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05290025 (Integration of Smoking Cessation Into Standard Treatment for People Receiving Opioid Agonist Therapy Who Are Smoking Tobacco), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 45% 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.

NCT05290025 naactive not recruitingnot on this map

Integration of Smoking Cessation Into Standard Treatment for People Receiving Opioid Agonist Therapy Who Are Smoking Tobacco: Protocol for a Randomised Controlled Trial

TypeinterventionalSponsorHaukeland University HospitalRan2022 to 2026Enrolled266ConditionsSmoking Cessation, Substance-Related DisordersArmsNicotine patch, Nicotine gum, Nicotine lozenge, Smoking cessation counselling, Screening for use of tobacco products
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Karl Trygve Druckrey-FiskaaenDepartment of Addiction Medicine, Bergen Addiction Research, Haukeland University Hospital, Bergen, Norway. karl.trygve.druckrey-fiskaaen@helse-bergen.no.ORCID http://orcid.org/0000-0002-2905-0613
Tesfaye MadeboDepartment of Addiction Medicine, Bergen Addiction Research, Haukeland University Hospital, Bergen, Norway.
Jan Tore DaltveitDepartment of Addiction Medicine, Bergen Addiction Research, Haukeland University Hospital, Bergen, Norway.
Jørn Henrik VoldDepartment of Addiction Medicine, Bergen Addiction Research, Haukeland University Hospital, Bergen, Norway.
Einar FurulundDepartment of Addiction Medicine, Bergen Addiction Research, Haukeland University Hospital, Bergen, Norway.
Torgeir Gilje LidCentre for Alcohol and Drug Research, Stavanger University Hospital, Stavanger, Norway.
Lars Thore FadnesDepartment of Addiction Medicine, Bergen Addiction Research, Haukeland University Hospital, Bergen, Norway.
Haukeland University Hospital · NOStavanger University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This protocol paper presents an updated statistical analysis plan of the protocol of a randomised controlled trial. The randomised controlled trial investigates the effect of integrating smoking cessation interventions at outpatient opioid agonist therapy (OAT) clinics for persons with opioid dependency receiving OAT medication. The intervention group receives weekly follow-up including a short behavioural intervention and provision of nicotine replacement products. The control group receives standard treatment. The duration of the intervention is 16 weeks and the follow-up was completed by the end of October 2023. The primary outcome is defined as the proportion of participants reducing the number of cigarettes smoked by at least a 50% at week 16 of the intervention period. The primary outcome will be analysed according to intention-to-treat principles. Missing outcome data will be set equal to the baseline values. Development and reporting of the statistical analysis plan follow the Guidelines for the Content of Statistical Analysis Plans in Clinical Trials.Trial registration ClinicalTrials.gov NCT05290025. Registered on 22 March 2022.

Indexed as

Smoking CessationAnalgesics, OpioidBehavior TherapyHumansRandomized Controlled Trials as TopicSmokingTobacco Use Cessation DevicesAnalgesics, OpioidOpioid agonist treatmentRandomised controlled trialSmoking cessationStatistical analysis plan

Identifiers

PMID38184633
PMCPMC10770886
OpenAlexW4390638541

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.