Akbari 2017.
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 Imputation of missing data: not specified |
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Participants |
Country: Iran Setting: university Age: mean = 21.58 (SD = 5.12); range = 18 ‐ 27 years Sample size (randomised): 30 Sex: 18 women, 12 men Comorbidity (mean (SD) of respective measures in indicated, if available): not specified Population description: nursing and midwifery students Inclusion criteria: 1) willingness to participate in the study; 2) no history of mental illnesses; 3) low happiness score; 4) high aggression score Exclusion criteria: 1) unwillingness to participate in the study; 2) diagnosed psychological disorders; 3) use of psychotropic medications and sedatives Attrition (withdrawals and exclusions): not specified Reasons for missing data: not specified |
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Interventions |
Intervention: resilience training (n = 15)
Control: no intervention (n = 15) |
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Outcomes |
Outcomes collected and reported:
Time points measured and reported: 1) pre‐intervention; 2) post‐intervention; only 2) post‐intervention reported Adverse events: not specified |
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Notes |
Contact with authors: We contacted the study authors to get the information about potential attrition and missing data in the study, the pre‐test means and SDs for both outcomes. We also inquired whether the means reported for happiness in Table 2 for the 2 groups were correct (lower score in IG compared to CG, but in the text the authors reported an increase of happiness through resilience training). We received no response to 2 inquiries. Study start/end date: not specified; study conducted during academic years 2013 ‐ 2014 Funding source: Islamic Azad University of Rasht Branch (see trial registration) Declaration of interest: not specified Ethical approval needed/obtained for study: approved by the Islamic Azad University (51172910725013) Comments by study authors: paper obtained from a research project approved by the Islamic Azad University of Rasht Branch; registered in the Iranian Registry of Clinical Trials (IRCT2016112231016N1) Miscellaneous outcomes by the review authors: not relevant Correspondence: Bahman Akbari; Department of Psychology, Rasht branch, Islamic Azad University, Rasht, Iran; Bakbari44@yahoo.com |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "Then they were randomly assigned to the intervention and control groups (15 per group)." Judgement comment: insufficient information about random‐sequence generation to permit judgement of ‘Low risk’ or ‘High risk’; no information about comparability of groups at baseline or respective analysis |
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; however, 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 | Unclear risk | Judgement comment: insufficient reporting of attrition/exclusions to permit judgement of ‘Low risk’ or ‘High risk’ (e.g. unclear if there were any missing data in the 2 groups; unclear how many participants were analysed) |
Selective reporting (reporting bias) | High risk | Judgement comment: trial registration (IRCT2016112231016N1) available and all of the study’s prespecified outcomes have been reported but only post‐intervention assessment is reported and time effect is not considered in MANCOVA |