Effects of participatory workplace improvement program on stress-related biomarkers and self-reported stress among university hospital nurses: a preliminary study

• Published in: Industrial Health Vol. 59; no. 2; pp. 128 - 141
• Main Authors: TONDOKORO, Tsukumi, NAKATA, Akinori, OTSUKA, Yasumasa, YANAGIHARA, Nobuyuki, ANAN, Ayumi, KODAMA, Hiromi, SATOH, Noriaki
• Format: Journal Article
• Language: English
• Published: Japan National Institute of Occupational Safety and Health 01.01.2021; National Institute of Occupational Safety and Health, Japan; National Institute of Occupational Safety and Health, Japan (JNIOSH)
• Subjects: Autonomic nervous activity; Biomarkers; Field Report; Focus group interview; Health aspects; Hospitals, University; Human resource management; Inflammation; Inflammatory markers; Interferon; Interleukin 12; Interleukin 15; Job stress; Management; Nurses; Occupational health; Occupational stress; Participatory management; Participatory workplace improvement program; Psychological aspects; Psychological stress; Stress; Voting; Wellness programs; γ-Interferon; Japan; Job stress; Participatory workplace improvement program; Voting; Focus group interview; Nurses; Inflammatory markers; Autonomic nervous activity
• DOI: 10.2486/indhealth.2020-0176
• ISSN: 0019-8366

Although participatory workplace improvement programs are known to provide favorable effects on high stress occupations like nursing, no studies have confirmed its effect using biomarkers. The aim of this study was to determine whether a participatory workplace improvement program would decrease stress-related symptoms as evaluated by biomarkers and self-reported stress among hospital nurses. Three actions to alleviate job stress, which were determined through focus group interviews and voting, were undertaken for two months. A total of 31 female Japanese nurses underwent measurement of inflammatory markers, autonomic nervous activity (ANA), and perceived job stress (PJS) at three-time points; before the program (T1), within a week after the completion of the program (T2), and three months after the program (T3). A series of inflammatory markers (Interferon-γ, Interleukin (IL)-6, and IL-12/23p40) decreased significantly at T2, and IL-12/23p40 and IL-15 significantly decreased at T3 compared to T1, while ANA and PJS remained unchanged. Our participatory program exerted beneficial effects in reducing inflammatory responses, but not for ANA and PJS. Further investigations with a better study design, i.e., a randomized controlled trial, and a larger sample size are warranted to determine what exerted beneficial effects on inflammatory markers and why other outcomes remained unchanged.