Be Well at Work-Plus: A Depression and Physical Activity Intervention for Hospital Service Workers (Aim 2)

Depression and physical inactivity are leading contributors to cardiometabolic diseases such as obesity, diabetes, and cardiovascular disease. Low-wage workers, who comprise one third of all workers in the U.S. and are essential to many industries, are more likely to be physically inactive and to have cardiometabolic conditions and depression, yet the participants are half as likely as higher wage workers to utilize preventive care. Targeted workplace initiatives have been successful in improving employee health, but low-wage workers are difficult to engage, in part due to a high burden of social disadvantage (e.g., food and housing insecurity, time and financial constraints). There are few, if any, workplace interventions for depression that specifically target low-wage workers and the participants unique social risk factors. This study was conceptualized using a planned adaptation approach that involves low-wage workers in the design of the intervention to increase engagement and feasibility. The study will test an evidence-based 8-session telephone-delivered depression intervention for working adults, Be Well at Work, and critical adaptations for low-wage workers: assessment and referrals for social determinants of health (e.g., food and housing insecurity, financial stress), physical activity promotion, and personalized text message behavioral support. The adapted intervention, Be Well at Work-PLUS, will be tested first in a single-arm open pilot (N=10) with exit interviews to refine the intervention content and delivery. Later, a pilot randomized controlled trial comparing Be Well at Work-PLUS to a waitlist condition (N=60) will be conducted (separate ClinicalTrials.gov study). The primary objectives are to assess acceptability, feasibility, and preliminary clinical outcomes. The primary preliminary clinical outcome is depression symptom severity, and secondary outcomes are physical activity, sleep quality, blood pressure, and BMI).

• Depression symptoms [Срок оценки: From baseline through end of treatment (approximately 4 months after enrollment).]
• Work limitations [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]
• Perceived stress [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]
• Sleep quality [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]
• Physical activity - step count [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]
• Body mass index (BMI) [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]
• Blood pressure [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]
• Physical activity - self report [Срок оценки: From baseline to end of treatment (approximately 4 months after enrollment)]