| Literature DB >> 27009060 |
Marylou Murray1, Lois Murray2, Michael Donnelly3,4.
Abstract
BACKGROUND: The health of doctors who work in primary care is threatened by workforce and workload issues. There is a need to find and appraise ways in which to protect their mental health, including how to achieve the broader, positive outcome of well-being. Our primary outcome was to evaluate systematically the research evidence regarding the effectiveness of interventions designed to improve General Practitioner (GP) well-being across two continua; psychopathology (mental ill-health focus) and 'languishing to flourishing' (positive mental health focus). In addition we explored the extent to which developments in well-being research may be integrated within existing approaches to design an intervention that will promote mental health and prevent mental illness among these doctors.Entities:
Keywords: General practitioners; Mental health; Primary care; Well-being
Mesh:
Year: 2016 PMID: 27009060 PMCID: PMC4806499 DOI: 10.1186/s12875-016-0431-1
Source DB: PubMed Journal: BMC Fam Pract ISSN: 1471-2296 Impact factor: 2.497
Summary of excluded studies
| Reason for exclusion | Number | Studies |
|---|---|---|
| Population not GPs | 6 | Bolton 2001; Hankir 2014; O’Reilly 2007; Ospina-Kammer(from Krasner); Rahe 2002; Rowe 1999 |
| No intervention | 11 | Bluestein 2011 - |
| Uncontrolled before and after study | 7 | Dunn 2007 (from Gardiner [ |
| Cohort study | 4 | Place 2013; Ro 2007; Ro 2010; Ro 2012 |
| Qualitative evaluation | 1 | Schneider 2014 |
| TOTAL | 29 |
Included studies
| Author/Year | Country | Population | Intervention | Comparator | Study design | Outcome measures/Timepoints | Numbers analysed | Results |
|---|---|---|---|---|---|---|---|---|
| Gardiner et al. [ | Australia | 86 GPs elected to attend a cognitive behavioural management course for which they gained Continued Professional Development | 15 h over 5 weeks. Cognitive behavioural management. | 24 GPs attending similar length CPD courses. Reported as being slightly older. | Controlled before and after study | Work-related distress (WRD -7 items Max score 49 = high distress)) |
| WRD- Higher = more distress |
| Gardiner et al. [ | Australia | 312 Rural GPs in reference group used to determine actual retention rate; | 9 h Work/life balance retreat. | Baseline data from RDWA survey reported in Gardiner 2005. | Controlled before and after study. | Rural Doctor Distress (RDD) |
| Rural Doctor Distress (RDD) |
| Holt & Del Mar [ | Australia | 819 GPs respondents to questionnaire | Aim | Questionnaire respondents with GHQ-12 score ≥3 were divided into 2 groups. | Controlled trial | GHQ-12 item |
| GHQ-12 scores |
| Martin Asuero et al. [ | Spain | 68 Primary care professionals elected to attend a mindfulness education programme. | 28 h over 8 weeks. Mindfulness-based group psychoeducational activities. | 25 Primary care professionals who were offered the intervention after study completion. | Controlled clinical trial | Maslach Burnout Inventory (MBI) 22items 3 subscales. Higher scores on emotional exhaustion and depersonalization; lower scores on personal accomplishment indicate a higher degree of burnout. Possible scores 0-140 |
| MBI |
Risk of bias
| Bias | Gardiner et al. [ | Holt and Del Mar | Gardiner et al. [ | Asuero et al. [ |
|---|---|---|---|---|
| Random sequence generation | High – Allocation by preference of participant | Unclear –Insufficient information provided about sequence generation | High – Allocation by judgement of participant | Unclear – Insufficient information provided about sequence generation |
| Allocation Concealment | High – Explicitly unconcealed procedure | Unclear – Insufficient information provided | High – Explicitly unconcealed procedure | Unclear-Insufficient information provided |
| Blinding of participants and personnel (performance bias) | High – Blinding of participants and personnel was not possible | High – Blinding of participants and personnel was not possible | High – Blinding of participants and personnel was not possible | High – Blinding of participants and personnel was not possible |
| Blinding of outcome assessment | High – Self-reported outcomes | High – Self-reported outcomes | High – Self-report for Rural Doctor Distress and Intention to leave. | High Self-reported outcomes |
| Incomplete outcome data | Unclear – Insufficient reporting of attrition to justify ‘low’ risk | Low – Clear participant flow reported | Unclear – Insufficient reporting of attrition to justify ‘low’ risk | Unclear–Baseline table indicates there were dropouts in the intervention group. No details provided |
| Selective reporting | Low – The published report includes all expected outcomes | Low – All outcomes reported | Low – The published report includes all expected outcomes | Low-All outcomes reported. |
| Other bias | Unclear – Insufficient information to assess whether other important risk of bias exits | High – Concurrent educational program effecting 26 participants. 14 in intervention group did not receive the intervention as a consequence. Control group contamination possible. | Unclear – Insufficient information to assess whether another important risk of bias exits |
Quality assessment using EPHPP tool for quantitative studies
| Components | Gardiner et al [ | Holt and Del Mar [ | Gardiner et al [ | Asuero et al. [ |
|---|---|---|---|---|
| Selection Bias 1. Are the individuals selected to participate likely to be representative of the target populations? | Self-referred/elected therefore using dictionary definition this scores | Participants were those respondents to a questionnaire found to score above a threshold. Questionnaire sent to all GPs in 8 Divisions of General Practice in Australia. 2 = Somewhat likely | Self-referred therefore using dictionary definition this scores 3 = NOT LIKELY | Self-referred/elected to attend. Subsequent stratified randomization reported. |
| Selection Bias 2. What percentage of the selected individuals agreed to participate? | 1 = 80-100 %. By electing to attend participants were agreeing to participate. | Baseline questionnaire response rate 819/1356 = 60 % | 69 Volunteered to attend but cannot tell how many actually participated 5 = Can’t tell | 1 = 80-100 % |
| SELECTION BIAS RATING | WEAK | MODERATE | WEAK | MODERATE |
| Study design | Controlled before and after study | Controlled clinical trial | Controlled before and after study | Controlled clinical trial |
| Was the study described as randomized? | No | Yes | No | Yes |
| Was the method of randomization described? | No | No | No | No |
| Was the randomization process appropriate? | Not applicable | No | Not applicable | No |
| STUDY DESIGN RATING | MODERATE | MODERATE | MODERATE | MODERATE |
| Were there important differences between groups prior to the intervention? | 1 = Yes | 3 = Can’t tell | 3 = Can’t tell. Control group for psychological well-being outcome were respondents to a survey. Control group for actual retention were entire population of rural GPs . | 3 = Can’t tell |
| What percentage of relevant confounders were controlled? | Can’t tell = 4 Controlling for confounders not explicit. | Can’t tell = 4 | Can’t tell = 4 | Can’t tell = 4 |
| CONFOUNDERS RATING | WEAK | WEAK | WEAK | WEAK |
| Were the outcome assessors aware of the intervention status of participants? | Yes = 1 | Yes = 1 | Yes = 1 | Yes = 1 |
| Were the participants aware of the research question? | Yes = 1 | Yes = 1 | Yes = 1 | Yes = 1 |
| BLINDING RATING | WEAK | WEAK | WEAK | WEAK |
| Were data collection tools shown to be valid? | Yes = 1 | Yes = 1 | Yes = 1 | Yes = 1 |
| Were data collections tools shown to be reliable? | Yes = 1 | Yes = 1 | Yes = 1 | Yes = 1 |
| DATA COLLECTION RATING | STRONG | STRONG | STRONG | STRONG |
| Were withdrawals and drop-outs reported in terms of numbers/reasons? | Yes = 1 | Yes = 1 | No = 2 | No = 2 Drop-outs from intervention group mentioned in baseline table. No details provided however results in scales approximate in remainder of tables. |
| Percentage of participants completing the study | 84 % = 1 | 161/233 = 69 % = 2 | 57 % = 3 | 100 % = 1 |
| WITHDRAWALS AND DROP OUTS RATING | STRONG | MODERATE | WEAK | STRONG |
| What percentage of participants received the allocated intervention? | Follow-up data for 77. Cannot tell if all 86 received the intervention. | 106/120 = 88 % | 48/68 = 60 % | 100 % |
| Was the consistency of the intervention measured? | Not explicitly | Not explicitly | Not explicitly | Described as ‘ |
| Is it likely that subjects received an unintended intervention that may influence results? | No = 5 | Yes = 4 | No = 5 | No = 5 |
| Unit of allocation | Individual | Individual | Individual | Individual |
| Unit of analysis | Individual | Individual | Individual | Individual |
| Are the statistical methods appropriate for the study design? | Yes = 1 | Yes = 1 | Yes = 1 | Yes = 1 |
| Is the analysis performed by intervention allocation status (ITT) rather than actual intervention received? | No = 2 | Yes = 1 | No = 2 | No = 1 |
Summary of Global rating for Quality using EPHPP Quality Assessment tool for Quantitative Studies
| Component | Gardiner et al [ | Holt and Del Mar [ | Gardiner et al [ | Asuero et al. [ |
|---|---|---|---|---|
| Selection Bias | Weak | Moderate | Weak | Moderate |
| Study Design | Moderate | Moderate | Moderate | Moderate |
| Confounders | Weak | Weak | Weak | Weak |
| Blinding | Weak | Weak | Weak | Weak |
| Data Collection Methods | Strong | Strong | Strong | Strong |
| Withdrawals and Dropouts | Strong | Moderate | Weak | Strong |
| GLOBAL RATING | WEAK | WEAK | WEAK | WEAK |
Criteria for global rating; 1. Strong = no weak ratings 2. Moderate = one weak rating, 3. Weak = two or more weak ratings