Key result
Planned ASCHR trial tests if telemedical smoking cessation increases quit rates ~10% in PAD.
Why the study?
Research on smoking cessation interventions in patients with peripheral arterial disease remains scarce and inconclusive regarding their efficacy.
Does an eight-month telemedical-psychological smoking cessation program improve smoking cessation rates in active smokers with peripheral arterial disease?
RCT (n=1,032)
Open-label
1:1 allocation ratio via an Interactive Web Response System (IWRS), stratified by treating clinics
Yes
Does an eight-month telemedical-psychological smoking cessation program improve smoking cessation rates in active smokers with peripheral arterial disease?
Answers are grounded in this paper and cite their sources.
This study protocol describes a randomized controlled trial evaluating a telemedical-psychological smoking cessation program tailored for patients with peripheral arterial disease.
BACKGROUND: Smoking is a major risk factor of cardiovascular diseases, notably peripheral arterial disease (PAD). Despite this link, research on smoking cessation interventions in PAD patients remains scarce and inconclusive regarding the efficacy of such interventions. Therefore, elucidating it is crucial and should address both individuals who smoke that are motivated to quit and individuals who smoke heavily lacking the motivation to quit. METHODS/DESIGN: The Aachen Smoking Cessation and Harm Reduction (ASCHR) trial is a prospective randomized controlled study (RCT) on the benefits of telemedical-psychological support for smoking cessation in patients with PAD, funded by the "Innovation Fund" of the Joint Federal Committee in Germany. This trial aims to scientifically assess the efficacy, feasibility, acceptance, and efficiency of a multi-stage smoking cessation program based on the recommendations of the German guideline for smoking cessation tailored to patients with PAD, compared to a control group receiving no intervention. Central to the program is psychological counseling utilizing motivational interviewing techniques, delivered through telemedicine via video consultations. The primary endpoint of the ASCHR trial is the smoking cessation rate after 8 months of intervention, with a secondary endpoint evaluating sustained abstinence at a further 6 months follow-up. Smoking cessation is defined as a carbon monoxide level in exhaled air of less than 6 ppm. We hypothesize that the group receiving the multi-stage cessation program will yield a cessation rate at least 10 percentage points higher than that of usual care. Anticipating a dropout rate of around 35%, the planned sample size is at least N = 1032 study participants. DISCUSSION: Should the trial demonstrate significant positive outcomes, efforts should be made to integrate the program into routine care in Germany, potentially offering a promising base for future smoking cessation support among PAD patients.
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Scheliga et al. (2024) conducted an RCT in Peripheral arterial disease (PAD) (n=1,032). Multi-stage telemedical-psychological smoking cessation program vs. Usual care was evaluated on Smoking cessation rate at 8 months (carbon monoxide level < 6 ppm).
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