Seligman 2007.
Methods | Study design: RCT Study grouping: parallel group Unit of randomisation: individuals Power (power & sample size calculation, level of power achieved): not specified Imputation of missing data: not specified; available‐case analysis (only participants for whom outcomes were obtained) |
Participants | Country: USA Setting: recruited from college; training setting in part probably University of Pennsylvania for classroom‐based workshops, also web‐based materials and e‐mail coaching Age: not specified Sample size (randomised): 240 Sex: 156 women, 84 men Comorbidity (mean (SD) of respective measures in indicated, if available) at baseline: depression (BDI): IG: 9.8 (5), CG: 10.4 (5.7); all participants with BDI score 9 ‐ 24 (mild to moderate depressive symptoms); anxiety (BAI): IG: 10 (5.7), CG: 11.8 (7.6) Population description: first‐year undergraduates at the University of Pennsylvania Inclusion criteria: 1) at risk for depression by virtue of scoring between 9 and 24 on the BDI, which are considered mild to moderate levels of depressive symptoms; 2) read and sign the voluntary consent form Exclusion criteria: BDI score above 24 (as these individuals were more likely to be in a current major depressive episode, and the purpose of the study was to prevent depression, not to treat current depression; 1.5% above 24) Attrition (withdrawals and exclusions): 13 lost to follow‐up: pre‐intervention (IG: 11, CG: 2); post‐intervention: no further loss to follow‐up; 6 further losses at 1‐ follow‐up (IG: 4, CG: 2); 9 further losses at 2‐ follow‐up (IG: 6, CG: 3); over total study course: 28 lost to follow‐up (IG: 21: CG: 7); attrition rate often exceeds 5.4% Reasons for missing data: too busy; studying abroad for 1 or 2 semesters |
Interventions |
Intervention: cognitive‐behavioral workshop along with web‐based materials and e‐mail coaching (n = 113)
Control: no intervention (n = 127)
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Outcomes |
Outcomes collected and reported:
Time points measured and reported: 1) pre‐intervention; 2) 2. assessment (end of fall semester in which 8‐week workshop took place); 3) 1. follow‐up (early in spring semester after intervention took place in fall semester); 4) 2. follow‐up (late in spring semester after intervention took place in fall semester) Adverse events: not specified |
Notes |
Contact with authors: We contacted the authors for how many weeks/months after the end of the intervention the 2. assessment and the 1. follow‐up took place (Schulman 2018 [pers comm]). We also asked whether healthcare students were included in the study, but received no response to this inquiry Study start/end date: mid‐ to late‐September (year not indicated) to end of spring semester (second follow‐up assessment); but planned to track participants 3 years Funding source: supported by grant MH63430 from the National Institute of Mental Health and by grant MH52270 from the National Institute of Mental Health Declaration of interest: The Penn Resilience Training for College Students is owned by the University of Pennsylvania. The University of Pennsylvania has licensed this program to Adaptiv Learning Systems. Dr Martin Seligman owns stock in Adaptiv and could profit from the sale of this program. The other researchers who collaborated on this project do not have a financial relationship with Adaptiv Ethical approval needed/obtained for study: not specified Comments by study authors: workshop manual developer and trainer of workshop leaders: Dr Karen Reivich; study is replication study of Seligman 1999 Miscellaneous outcomes by the review authors: unclear if healthcare students were included in the study Correspondence: Martin EP Seligman; University of Pennsylvania; 3720 Walnut Street, Solomon Labs, Philadelphia, PA 19104, USA; seligman@psych.upenn.edu |