Table 2. Primary and Secondary Efficacy Outcomes in the Intention-to-Treat Analysis.
Outcomes | Participants, No./Total No. (%) | RR (95% CI)a | P valueb | |
---|---|---|---|---|
SA group | NSA group | |||
Primary outcome, depression recovery at 3 mo vs baseline (n = 47)c,d | 14/24 (58) | 10/23 (43) | 1.34 (0.76-2.45) | .38 |
Secondary outcomes | ||||
Depression recovery at 4 wk vs baseline (n = 57) | 12/28 (43) | 9/29 (31) | 1.28 (0.74-2.14) | .42 |
Depression recovery at 6 wk vs baseline (n = 51) | 10/26 (38) | 10/25 (40) | 0.96 (0.53-1.65) | >.99 |
Symptom remission at 4 wk vs baseline (n = 57)e | 8/28 (28) | 5/29 (17) | 1.35 (0.72-2.20) | .36 |
Symptom remission at 6 wk vs baseline (n = 51) | 7/26 (27) | 5/25 (20) | 1.19 (0.61-2.00) | .74 |
Symptom remission at 3 mo vs baseline (n = 47) | 11/24 (46) | 3/23 (13) | 1.99 (1.16-3.34) | .02 |
Abbreviations: NSA, nonspecific auricular acupuncture; RR, risk ratio; SA, specific auricular acupuncture.
Effect size was calculated as RR for dichotomous data.
Statistical significance was calculated with Fisher exact test.
The primary outcome (improvement in depression symptoms) was defined as a reduction of 50% or more from baseline Patient Health Questionnaire-9 (PHQ-9) scores. The number of cases and proportions are based on observed data.
Depressive symptoms measured by PHQ-9 scores range from 0 (least) to 27 (greatest) symptom burden.
Participants who achieved a score less than 5 on the PHQ-9, indicating symptom remission.