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. 2022 Apr 14;2022(4):CD013696. doi: 10.1002/14651858.CD013696.pub2

Summary of findings 2. Acceptance and commitment therapy (ACT) compared with control for smoking cessation.

Acceptance and commitment therapy (ACT) compared with control for smoking cessation
Patient or population: people who smoke
Setting: community; online; primary care; high schools and universities (USA; Cyprus; Hong Kong; Ireland)
Intervention: Acceptance and commitment therapy (ACT)
Comparisons: matched‐intensity smoking cessation treatment; NRT; brief advice; less intensive ACT
Outcomes Anticipated absolute effects* (95% CI) Relative effect
(95% CI) № of participants
(studies) Certainty of the evidence
(GRADE) Comments
Risk with control Risk with ACT
ACT vs matched‐intensity smoking cessation treatment: smoking cessation (≥ 6‐month follow‐up) It was not appropriate to pool data across these studies because there was a high level of heterogeneity (I2 = 82%) and the result may be misleading.  5723
(5 RCTs)
⊕⊝⊝⊝
Very lowa,b,c  
ACT vs NRT: smoking cessation (≥ 6‐month follow‐up) Study population RR 1.27
(0.53 to 3.02) 102
(1 RCT) ⊕⊕⊝⊝
Lowd  
15 per 100 19 per 100
(8 to 45)
ACT vs brief advice: smoking cessation (≥ 6‐month follow‐up) Study population RR 1.27
(0.59 to 2.75) 144
(1 RCT) ⊕⊝⊝⊝
Very lowd,e  
14 per 100 17 per 100
(8 to 37)
ACT vs less intensive ACT: smoking cessation (≥ 6‐month follow‐up) Study population RR 1.00
(0.50 to 2.01) 100
(1 RCT) ⊕⊕⊝⊝
Lowd  
24 per 100 24 per 100
(12 to 48)
Mental health and well‐being One study that compared ACT with NRT found no clinically meaningful difference in negative affect across conditions at all follow‐ups to 12 months.
 
Another study that compared ACT with a matched‐intensity smoking cessation treatment and a less intensive ACT intervention found no clinically meaningful difference in positive mental health across conditions up to 6‐month follow‐up.
252
(2 RCTs)
⊕⊝⊝⊝
Very lowf,g We were unable to meta‐analyse this outcome and therefore summarised narratively.
*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

ACT: Acceptance and commitment therapy; CI: confidence interval; NRT: nicotine replacement therapy; RCT: randomised controlled trial; RR: risk ratio
GRADE Working Group grades of evidenceHigh certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect.

aDowngraded by two levels due to inconsistency: substantial heterogeneity was detected (I² = 82%). A subgroup analysis grouping by mode of delivery used explained a small amount of this, but substantial heterogeneity remained unexplained.
bNot downgraded for indirectness. One study included only smokers without health insurance, but contributed just 17.3% of the weighted effect.
cDowngraded by one level due to imprecision: the confidence interval of the effect estimate incorporates clinically relevant potential benefit and harm of the intervention.
dDowngraded by two levels due to imprecision: the overall number of events was very low (< 25) and the confidence interval of the effect estimate incorporates clinically relevant potential benefit and harm of the intervention.
eDowngraded by two levels due to risk of bias: we judged the sole study to be at high risk of bias.
fDowngraded by two levels due to inconsistency: the constructs and measures of mental health used differed across studies, as well as the study comparators.
gDowngraded by two levels due to imprecision: two small studies likely lacked sufficient statistical power to detect clinically meaningful effects.