Table 2.
Study characteristics grouped by control type
| Authors, year | Control type | Population | Mindfulness na |
Control nb |
Mindfulness intervention | Mindfulness intervention delivery mode | Comparison intervention | Comparison intervention delivery mode | Intervention duration | Intervention hoursc | Scale /V0 meand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Hesser et al., 2012 | SAC | Tinnitus | 35 | 32 | ACT | Web-based App | CBT | Web-based App | 8 weeks | 16 |
ISI 13.91 |
| Low et al., 2020 | SAC | Insomnia | 12 | 11 | MM | Mobile App | Progressive muscle relaxation | Mobile App | 40 or 60 dayse | 6.67 or 10 |
ISI 13.61 |
| Mak et al., 2017 | SAC | Young adults | 1041 | 1040 | MM | Web-based App | CBT | Web-based App | 8 weeks | 5 |
MOS-SS 26.49 |
| Boettcher et al., 2014 | NSAC | Anxiety disorders | 45 | 46 | MM | Web-based App | Discussion forum | Web-based App | 8 weeks | 16 |
ISI 11.74 |
| Hesser et al., 2012 | NSAC | Tinnitus | 35 | 32 | ACT | Web-based App | Discussion forum | Web-based App | 8 weeks | 16 |
ISI 13.49 |
| Messer et al., 2019 | UCC | Cancer survivors | 11f | 10f | MBSR | Web-based App | Usual care | NA | 6 weeks | 8 |
PSQI 11.57 |
| Simister et al., 2018 | UCC | Fibromyalgia | 33 | 34 | ACT | Web-based App | Usual care | NA | 8 weeks | NR |
PSQI 12.97 |
| Chapoutot et al., 2020 | Waitlist | Insomnia with hypnotic dependence | 16 | 16 | ACT-enhanced CBT | Video-conference | Waitlist | NA | 8 weeks | 4 |
PSQI 14.80 |
| Lappalainen et al., 2019 | Waitlist | Insomnia | 43 | 43 | ACT | Web-based App | Waitlist | NA | 6 weeks | NR |
ISI 16.96 |
| Nissen et al., 2020 | Waitlist | Cancer survivors | 104 | 46 | MBCT | Web-based App | Waitlist | NA | 8 weeks | NR |
ISI 11.73 |
| Querstret et al., 2017 | Waitlist | Working adults | 63 | 64 | MM | Web-based App | Waitlist | NA | 4 weeks | NR |
PSQI 11.26 |
ACT acceptance and commitment therapy, CBT cognitive behavioral therapy, ISI Insomnia Severity Index, MBCT mindfulness-based cognitive therapy, MBSR mindfulness-based stress reduction, MM mindfulness meditation, MOS-SS Medical Outcomes Study-Sleep Scale, NA not applicable, NR not reported, NSAC nonspecific active control, PSQI Pittsburgh Sleep Quality Index, SAC specific active control, UCC usual care control
aMindfulness sample size is reported as participants initially randomized to the intervention group
bControl sample size is reported as participants initially randomized to the control group
cMindfulness hours are reported as expected hours per intervention, excluding home practice
dThe V0 sleep quality mean score (i.e., baseline weighted average) was used to determine if each study cohort had clinically relevant sleep disturbance based on established cut-off scores
eDue to time constraints, some participants were asked to complete 40 days of mindfulness meditation instead of 60 days; both groups were combined in the analysis.-
fTwo participants dropped out of the study after randomization. The study did not report the two participants’ group affiliation; thus, the sample sizes reflect the number of participants who completed the intervention