Multi-Level Trial of a Workplace Sales Ban of Sugary Beverages and Brief Motivational Counseling Intervention on Adiposity
Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of the study is to test the impact of a multilevel workplace intervention (hospital-wide sales ban on sugar-sweetened beverages (SSBs) and individual-level brief counseling) on employee health.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:
• Full-time employee who works on campus at one of the Sutter Health participating sites
• Speaks and reads English
• Consumes three or more sugar-sweetened beverages (SSB) a week
• Agrees to participate in two fasting blood draws
Locations
United States
California
Sutter Health/California Pacific Medical Center Research Institute
RECRUITING
San Francisco
Contact Information
Primary
Sweet Study Contact
sweet@sutterhealth.org
415-600-5848
Time Frame
Start Date: 2023-08-01
Estimated Completion Date: 2025-10-01
Participants
Target number of participants: 700
Treatments
No_intervention: Control: No workplace SSB sales ban, no brief intervention
Participants receive no workplace SSB sales ban (environmental intervention) and no brief counseling intervention.
Experimental: Workplace SSB sales ban only
Participants receive a workplace SSB sales ban (environmental intervention). This entails the removal of SSBs from all workplace sales outlets, replacing them with non-sugary beverage options.
Experimental: Brief intervention only
Participants receive a 20-30 minute intervention by video call, with 2 booster telephone calls. One week and one month after the initial session, participants will have 10-minute check-in/booster phone calls.
Experimental: Multilevel Intervention (workplace SSB sales ban + brief intervention)
Sales ban: Participants receive a workplace SSB sales ban (environmental intervention). This entails the removal of SSBs from all workplace sales outlets, replacing them with non-sugary beverage options.~Brief Intervention: Participants receive a 20-30 minute intervention by video call, with 2 booster telephone calls. One week and one month after the initial session, participants will have 10-minute check-in/booster phone calls.
Related Therapeutic Areas
Sponsors
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Sutter Health, California Pacific Medical Center Research Institute
Leads: University of California, San Francisco