OBJECTIVE: The purpose of this study was to determine if a novel workplace stress management program, delivered either face-to-face or by self-help, would reduce illness and health services utilization among participants. METHODS:Five hundred one volunteers were randomly allocated to one of three groups: full intervention, which received assessment and personalized self-study feedback and was offered six face-to-face, small-group sessions; partial intervention, a self-help group that received assessment and personalized feedback by mail; and a wait-list control group. All participants completed questionnaires for stress, anxiety, and coping at the start of the study and 6 and 12 months later. Health reports were completed at 0, 3, 6, 9, and 12 months. A subsample of subjects who subscribed to a single health maintenance organization provided objectively recorded doctor visit data across the study year. RESULTS: All three groups reported significant improvement in their stress, anxiety, and coping across the year. Full intervention participants showed a more rapid reduction in negative responses to stress than did participants from the other groups. Full-intervention subjects also reported fewer days of illness than subjects in the other groups. Objectively measured physician visits showed a large (34%) reduction in healthcare utilization for full intervention subjects in the HMO subsample. CONCLUSIONS: These results indicated that a work-site program that focuses on stress, anxiety, and coping measurement along with small-group educational intervention can significantly reduce illness and healthcare utilization.
RCT Entities:
OBJECTIVE: The purpose of this study was to determine if a novel workplace stress management program, delivered either face-to-face or by self-help, would reduce illness and health services utilization among participants. METHODS: Five hundred one volunteers were randomly allocated to one of three groups: full intervention, which received assessment and personalized self-study feedback and was offered six face-to-face, small-group sessions; partial intervention, a self-help group that received assessment and personalized feedback by mail; and a wait-list control group. All participants completed questionnaires for stress, anxiety, and coping at the start of the study and 6 and 12 months later. Health reports were completed at 0, 3, 6, 9, and 12 months. A subsample of subjects who subscribed to a single health maintenance organization provided objectively recorded doctor visit data across the study year. RESULTS: All three groups reported significant improvement in their stress, anxiety, and coping across the year. Full intervention participants showed a more rapid reduction in negative responses to stress than did participants from the other groups. Full-intervention subjects also reported fewer days of illness than subjects in the other groups. Objectively measured physician visits showed a large (34%) reduction in healthcare utilization for full intervention subjects in the HMO subsample. CONCLUSIONS: These results indicated that a work-site program that focuses on stress, anxiety, and coping measurement along with small-group educational intervention can significantly reduce illness and healthcare utilization.
Authors: Heribert Limm; Peter Angerer; Mechthild Heinmueller; Birgitt Marten-Mittag; Urs M Nater; Harald Guendel Journal: BMC Public Health Date: 2010-05-14 Impact factor: 3.295
Authors: Pim Cuijpers; Tara Donker; Robert Johansson; David C Mohr; Annemieke van Straten; Gerhard Andersson Journal: PLoS One Date: 2011-06-21 Impact factor: 3.240
Authors: Lisa Lyssenko; Gerhard Müller; Nikolaus Kleindienst; Christian Schmahl; Mathias Berger; Georg Eifert; Alexander Kölle; Siegmar Nesch; Jutta Ommer-Hohl; Michael Wenner; Martin Bohus Journal: BMC Public Health Date: 2015-08-01 Impact factor: 3.295
Authors: Leona Tan; Min-Jung Wang; Matthew Modini; Sadhbh Joyce; Arnstein Mykletun; Helen Christensen; Samuel B Harvey Journal: BMC Med Date: 2014-05-09 Impact factor: 8.775