Peng 2014.
| Study characteristics | ||
| Methods |
Study design: RCT Study grouping: parallel group Unit of randomisation: individualsPower (power & sample size calculation, level of power achieved): not specifiedImputation of missing data: not specified |
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| Participants |
Country: ChinaSetting: medical students of Third Military Medical University; training setting not specifiedAge: mean = 19.78 (SD = 0.77); range = 18 ‐ 22 yearsSample size (randomised): 60; 30 divided into high‐resilience group (SD above average score of CD‐RISC (CD‐RISC)); n = 30, divided into low‐resilience group (SD below average score of CD‐RISC)Sex: 18 women, 42 menComorbidity (mean (SD) of respective measures in indicated, if available) at baseline: not specifiedPopulation description: medical students Inclusion criteria: not specified Exclusion criteria: not specified Attrition (withdrawals and exclusions): not specified Reasons for missing data: not specified |
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| Interventions |
Intervention: Penn Resilience Program (PRP) (in total: n = 30; n = 15 of high‐resilience group, n = 15 of low‐resilience group)
Control: wait‐list control (in total: n = 30; 15 of high‐resilience group, 15 of low‐resilience group) |
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| Outcomes |
Outcomes collected and reported:
Time points measured and reported: 1) pre‐intervention; 2) post‐intervention Adverse events: not specified |
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| Notes |
Contact with authors: We contacted the authors for the second full text, but received no response to 2 inquiries. Study start/end date: not specifiedFunding source: This study was financially supported by National Natural Science Foundation of China Granted to Min Li (No. 31170994) and Project of Military Research Foundation of PLA of China to Min Li (Grants 12XLZ212 and CWS11J049).Declaration of interest: not specifiedEthical approval needed/obtained for study: approved by the Ethics Committee of the Third Military Medical UniversityComments by study authors: not relevantMiscellaneous outcomes by the review authors: 2 reports; full text for 2. report not availableCorrespondence: Li Peng; corresponding author: Min Li; Department of Military Psychology, School of Psychology, The Third Military Medical University, No. 30, Gaotanyan Road, Shapingba District, Chongqing 400038, China, Tel.: +86 23 68752267; fax: +86 23 68752360; limin52267@tmmu.edu.cn (M. Li) |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Quote: "the students were divided into high‐resilience and low‐resilience groups, with each group consisting of 30 students. Half of the students from each group were then divided into the experimental group and received PRP training. The remaining students were divided into the control group and were told to wait for resilience training." Quote: "From them, 30 students with high resilience and 30 with low resilience were obtained. These students were further randomly assigned into experimental group to receive resilience training (n = 15), and control group without training (n = 15)." Quote: "No significant differences in resilience, positive emotion, negative emotion, cognitive appraisal, and expression inhibition scores were found between the control and experimental groups (P > .05) (see Table 2)." Judgement comment: insufficient information about random‐sequence generation to permit judgement of ‘Low risk’ or ‘High risk’; verified baseline comparability of groups for outcome variables on the basis of analysis (see Table 2; all Ps > 0.28 in high‐resilience participants or all Ps > 0.30 in low‐resilience individuals), baseline comparability for sociodemographic characteristics (e.g. age, gender) not specified |
| Allocation concealment (selection bias) | Unclear risk | Judgement comment: insufficient information about allocation concealment to permit a 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 | Low risk | Judgement: insufficient reporting of attrition/exclusions to permit judgement of 'Low risk' or 'High risk' (probably 30 randomised in each group were also analysed; but unclear if there were any missing data and if missing data were imputed) |
| Selective reporting (reporting bias) | Low risk | Judgement comment: no study protocol or trial registration available but it is clear that the published reports include all expected outcomes, including those that were prespecified |