Porter 2008.
| Study characteristics | ||
| Methods |
Study design: RCT Study grouping: parallel group Unit of randomisation: individuals Power (power sample size calculation, level of power achieved): not specified; according to publication maybe lack of statistical power Imputation of missing data: no imputation of missing data; available‐case analysis (only participants for whom outcomes were obtained at both time points) |
|
| Participants |
Country: Canada Setting: college programme for paramedic students Age: mean = 21.69 (SD = 1.92); range = 19 ‐ 28 years Sample size (randomised): 29 Sex: 11 women, 18 men Comorbidity (mean (SD) of respective measures in indicated, if available) at baseline: depression (SCL‐90‐R): IG: 1.08 (0.42); CG: 1.57 (0.65); Anxiety (SCSL‐90‐R): IG: 0.73 (0.49); CG: 0.93 (0.51); Global Severity Index (SCL‐90‐R): IG: 0.85 (0.33); CG: 1.09 (0.52); Burnout‐emotional exhaustion (MBI): IG:17.09 (6.72); CG: 20.64 (10.20); Burnout‐depersonalisation (MBI): IG: 8.82 (4.88); CG: 9.45 (3.86); Burnout‐personal accomplishment (MBI): IG: 34.64 (8.32); CG: 32.73 (8.36) Population description: paramedic students in the final year of a 2‐year college paramedic programme Inclusion criteria: not specified Exclusion criteria: not specified Attrition (withdrawals and exclusions): 6 participants dropped out of the study before post‐intervention assessment (IG: 3/15 (20%); CG: 3/14 (21.4%)); n = 1 participant did not complete WAYS measure Reasons for missing data: not specified |
|
| Interventions |
Intervention: psycho‐educational group (n = 15)
Control: no intervention (n = 14) |
|
| Outcomes |
Outcomes collected and reported:
Time points measured and reported: 1) pre‐intervention; 2) 2‐month follow‐up (2‐months post‐intervention; 6‐month interval between 2 assessments) Adverse events: not specified |
|
| Notes |
Contact with authors: We contacted authors for the number of dropouts and the number of participants analysed for each group at pre‐ and post‐intervention assessment (Porter 2018 [pers comm]). Study start/end date: recruitment start in fall 2007; exact study dates not specified Funding source: funding for this research provided by Fanshawe College Research Initiatives Fund Declaration of interest: not specified Ethical approval needed/obtained for study: not specified Comments by authors: not relevant Miscellaneous outcomes by the review authors: not relevant Correspondence: Shirley Porter; Fanshawe College, Student Success Centre, 1001 Fanshawe College Blvd., F2010, P.O. Box 7005, London, Ontario, Canada N5Y 5R6; saporter@fanshawec.ca |
|
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Quote: "Fourteen participants (8 women) were randomly assigned to be part of the control group, and fifteen participants (5 women) were randomly assigned to be part of the treatment group." Quote: "Ages ranged from 20 to 25 in the control group (M = 21.82, SD = 1.72), and from 19 to 28 in the treatment group (M = 21.58, SD = 2.31). This age difference was not statistically significant." Judgement comment: insufficient information about random‐sequence generation to permit judgement of ‘Low risk’ or ‘High risk’; verified baseline comparability for sociodemographic variable age; baseline comparability for other sociodemographic characteristics and outcomes of interest unclear |
| Allocation concealment (selection bias) | Unclear risk | Judgement comment: insufficient information about allocation concealment to permit judgement of ‘Low risk’ or ‘High risk’ |
| Blinding of participants and personnel (performance bias) Subjective outcomes | High risk | Judgement comment: blinding of participants and personnel probably not done (face‐to‐face intervention) and the outcome is likely to be influenced by lack of blinding |
| Blinding of outcome assessment (detection bias) Subjective outcomes | High risk | Judgement comment: insufficient information about blinding of outcome assessment; but due to potential performance bias (no blinding of participants), the review authors judge that the participants' responses to questionnaires may be affected by the lack of blinding (i.e. knowledge and beliefs about intervention they received) |
| Incomplete outcome data (attrition bias) All outcomes | High risk | Quote: "Six participants dropped out of the study before post‐test measures were collected. Three of these individuals (all men) were in the control group, and three of these individuals were in the treatment group (2 women)." Quote: "The final sample was, therefore, comprised of 23 individuals, 11 in the control group (8 women), and 12 in the treatment group (3 women)." Judgement comment: reasons for missing data unlikely to be related to true outcome with balance in missing data between groups (IG: n = 3; CG: n = 3); for burnout, attitudes toward emotional expression, peer support and ways of coping subscales: 1 additional missing participant; reasons for missing data not reported; available‐case analysis (only participants for whom outcomes were obtained at both time points) |
| Selective reporting (reporting bias) | Low risk | Judgement comment: no study protocol available but it is clear that the published reports include all expected outcomes, including those that were prespecified |