The mental health of health care workers (HCWs) is an important global concern, particularly in low- and middle-income countries (LMICs) such as Kenya, where unique stressors may place HCWs at disproportionate risk for depression.1 However, depression prevalence and risk factors in this population are not well understood. To address this gap, we evaluated the prevalence of depressive symptoms among Kenyan HCWs and identified associated demographic, psychological, and workplace factors.
Methods |
The Aga Khan University Institutional Scientific and Ethics Review Committee and recruitment sites approved this survey study. Participants provided electronic informed consent and were compensated 500 Kenyan shillings (US $3.86). The study followed the AAPOR reporting guideline.
We used longitudinal data collected from HCWs from 5 hospitals in Nairobi, Kenya, based on the Intern Health Study protocol.2 HCWs who enrolled in the longitudinal UZIMA-DS study beginning in April 2023 completed surveys at enrollment and quarterly for 12 months. The surveys assessed depressive symptoms using the 9-item Patient Health Questionnaire (PHQ-9) in English3 and other demographic, psychosocial, and workplace factors (eMethods in Supplement 1).4
We used a weighting strategy to reduce participant attrition biases (eMethods in Supplement 1). To capture potential variation, we assessed mean PHQ-9 scores and calculated the proportion of participants meeting PHQ-9 criteria for depression at each survey time point. We used Pearson correlations and χ2 tests to examine associations between demographic variables and PHQ-9 scores. Risk factors were entered into a stepwise linear regression model. To explore workplace factors associated with depressive symptoms, we included repeated measures of work hours, workplace discrimination, medical errors, and stressful life events in a generalized estimating equation (GEE) model. Significant demographic and personality variables were added as covariates. Analyses were conducted in R, version 4.4.1 (R Project for Statistical Computing). Two-sided P < .05 was considered significant.
Results |
Among 527 enrolled participants, 514 (97.5%) completed the PHQ-9 questionnaire at enrollment and were included in the analysis (mean [SD] age, 34.1 [8.1] years; 340 women [66.1%] and 174 men [33.9%]) (Table 1 and eFigure in Supplement 1). At 3, 6, 9, and 12 months, 197 (38.3%), 211 (41.1%), 210 (40.9%), and 177 (34.4%) participants completed the depressive symptom surveys, respectively.
Table 1.
Participant Characteristicsa
| Characteristic | Unweighted value (N = 514) | Weighted value (N = 514)b |
|---|---|---|
| Demographic factors | ||
| Age, mean (SD), y | 34.1 (8.1) | 34.0 (9.7) |
| Sex | ||
| Female | 340 (66.1) | 339 (66.0) |
| Male | 174 (33.9) | 175 (34.0) |
| Profession | ||
| Physician | 39 (7.6) | 41 (8.0) |
| Nurse | 303 (58.9) | 317 (61.7) |
| Other | 172 (33.5) | 156 (30.4) |
| Relationship status | ||
| In a committed relationship | 388 (75.5) | 389 (75.7) |
| Not in a committed relationship | 126 (24.5) | 125 (24.3) |
| No. of children, mean (SD) | 1.5 (1.1) | 15 (1.3) |
| Neuroticism, mean (SD) | 30.8 (7.7) | 30.8 (8.5) |
| Difficult early family environment, mean (SD) | 19.0 (13.1) | 19.0 (16.2) |
| Years of work experience, mean (SD), y | 9.7 (6.9) | 9.7 (8.2) |
| Psychosocial and workplace factors | ||
| Work hours, mean (SD) | 54.2 (24.8) | 55.0 (33.9) |
| Medical errors | ||
| Yes | 31 (6.0) | 31 (6.0) |
| No | 483 (94.0) | 483 (94.0) |
| Workplace discrimination | ||
| Yes | 220 (42.8) | 242 (47.1) |
| No | 294 (57.4) | 272 (52.9) |
| Stressful life events | ||
| Yes | 321 (62.5) | 330 (64.2) |
| No | 193 (37.5) | 184 (35.8) |
Unless noted otherwise, values are reported as No. (%) of participants.
A weighting strategy was used to reduce participant attrition biases.
After attrition weighting, 175 (34.0%), 51 (26.0%), 44 (21.0%), 47 (22.5%), and 32 (17.9%) participants met PHQ-9 criteria (≥10) for major depression at enrollment and at 3, 6, 9, and 12 months, respectively. A total of 222 participants (43.1%) met PHQ-9 criteria at 1 or more quarterly assessments, with 87 (16.9%) and 28 (5.5%) meeting criteria for moderately severe (≥15) and severe (≥20) depression.
Among demographic and personality factors established as risk factors for PHQ-9 score increase among medical residents in previous studies2 and 1 context-specific factor, age (r = −0.09; P = .04), neuroticism (r = 0.54; P < .001), difficult early family environment (r = 0.42; P < .001), relationship status (r = −0.16; P < .001), and years of work experience (r = −0.08; P = .04) were associated with depressive symptoms. In GEE analysis, neuroticism, difficult early family environment, relationship status, stressful life events, and workplace discrimination were associated with increased depressive symptoms (Table 2).
Table 2.
Factors Associated With Increased Depressive Symptoms
| Factor | β (95% CI) | p value |
|---|---|---|
| Demographic factors | ||
| Age | −0.02 (−0.08 to 0.04) | .48 |
| Female sex | 0.23 (−0.46 to 0.91) | .52 |
| Profession | ||
| Nurse vs physician | −0.61 (−1.60 to 0.39) | .23 |
| Other vs physician | −0.14 (−1.22 to 0.95) | .80 |
| In a committed relationship | −0.96 (−1.82 to −0.11) | .03 |
| Neuroticism | 0.22 (0.18–0.27) | <.001 |
| Difficult early family environment | 0.07 (0.04–0.10) | <.001 |
| Years of work experience | 0.06 (−0.41 to 0.54) | .79 |
| Psychosocial and workplace factors | ||
| Work hours | 0.16 (−0.05 to 0.38) | .14 |
| Medical errors | 1.13 (−0.17 to 2.43) | .09 |
| Workplace discrimination | 1.95 (1.36–2.54) | <.001 |
| Stressful life events | 2.51 (1.98–3.05) | <.001 |
Discussion |
In this 12-month survey study of Kenyan HCWs using validated measures and an established protocol, 43.1% of participants met PHQ-9 criteria for major depression—a rate notably higher than that reported for HCWs in Europe and North America and in the general Kenyan population.5,6 Consistent with previous studies,2 risk factors for depression were higher neuroticism, not being in a committed relationship, having a difficult early family environment, experiencing stressful life events, and experiencing workplace discrimination. Unlike findings from US studies,2 work hours and medical errors were not associated with depression.
Potential limitations include underreporting and lack of generalizability beyond nurses and physicians in Nairobi. These findings underscore the need for culturally tailored mental health interventions that address key individual and contextual risk factors for HCWs in LMICs.
Supplementary Material
Funding/Support:
This study was supported by the NIH Office of the Director, the National Institute of Biomedical Imaging and Bioengineering, the National Institute of Mental Health, and the Fogarty International Center under award number U54TW012089 (Dr Waljee and Prof Abubakar).
Role of the Funder/Sponsor:
The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Additional Contributions:
We acknowledge all of the Kenyan health care workers who participated in this study.
Footnotes
Conflict of Interest Disclosures: Dr Waljee reported receiving grants from the National Institutes of Health (NIH) during the conduct of the study. Dr Ngugi reported receiving grants from the NIH during the conduct of the study. No other disclosures were reported.
Disclaimer: The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Contributor Information
Andrew Aballa, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya.
Dorcas G. Mwigereri, Department of Population Health, Aga Khan University, Nairobi, Kenya.
Zhuo Zhao, Michigan Neuroscience Institute, University of Michigan Medical School, Ann Arbor.
Willie Njoroge, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya.
Linda Khakali, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya.
Rachel Maina, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya.
David Andai, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya.
James Orwa, Department of Population Health, Aga Khan University, Nairobi, Kenya.
Amos Bunde, Computing and Data Innovation Office, Aga Khan University, Nairobi, Kenya.
Eileen M. Weinheimer-Haus, Center for Global Health Equity, University of Michigan, Ann Arbor; Department of Learning Health Sciences, University of Michigan Medical School, Ann Arbor; Michigan Integrated Center for Health Analytics and Medical Prediction, University of Michigan, Ann Arbor.
Jessica Baker, Department of Learning Health Sciences, University of Michigan Medical School, Ann Arbor.
Lukoye Atwoli, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya; Department of Medicine, Medical College East Africa, Aga Khan University, Nairobi, Kenya.
Srijan Sen, Michigan Neuroscience Institute, University of Michigan Medical School, Ann Arbor.
Akbar K. Waljee, Center for Global Health Equity, University of Michigan, Ann Arbor; Department of Learning Health Sciences, University of Michigan Medical School, Ann Arbor; Michigan Integrated Center for Health Analytics and Medical Prediction, University of Michigan, Ann Arbor.
Anthony K. Ngugi, Department of Population Health, Aga Khan University, Nairobi, Kenya.
Amina Abubakar, Institute for Human Development, Aga Khan University, Nairobi, Kenya; Neurosciences Unit, Kenya Medical Research Institute, Wellcome Trust Research Programme, Kilifi, Kenya.
Zhenke Wu, Department of Biostatistics, University of Michigan, Ann Arbor.
Zul Merali, Brain and Mind Institute, Aga Khan University, Nairobi, Kenya.
Elena Frank, Michigan Neuroscience Institute, University of Michigan Medical School, Ann Arbor.
Data Sharing Statement:
See Supplement 2.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
See Supplement 2.
