Stand & Move at Work II: Effectiveness and Implementation of a Worksite Wellness Program
- Conditions
- Sedentary Behavior
- Interventions
- Behavioral: Stand & Move at Work+Behavioral: Stand & Move at Work
- Registration Number
- NCT05485675
- Lead Sponsor
- Arizona State University
- Brief Summary
This is a 2-arm group-randomized hybrid effectiveness-implementation (HEI type 2) study to test an evidence-based intervention (EBI) known as Stand \& Move at Work(SMW) to reduce sedentary time in the workplace, and to test the role of expert facilitation (SMW+) for improving intervention fidelity.
- Detailed Description
Primary Aim: To assess worksite-level reduction in sedentary time and intervention fidelity over 12 months Secondary Aim: To assess cost effectiveness of the intervention at 12 and 24 months
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 4800
- More than 80% of employees work full time (30+ hours per week).
- At least 45 employees in the worksite with sit-stand workstations working at least three days per week
- Occupations require primarily desk-based work (e.g., computer- and telephone-based)
- Willing to allow the researchers to distribute online research surveys to all employees in order to allow the program to be evaluated.
- Allow 30 randomly selected individuals to wear an activity monitor in several 7-day intervals across two years.
- Willing to be randomized to either intervention.
- Willing to identify one or more worksite champions to implement the Stand & Move at Work™ program.
Worksite-level exclusion criteria:
- Involved in previous interventions to reduce sitting and increase standing and moving at work in the last 24 months.
- Involved in the Stand and Move I intervention.
- Another worksite within the same organization is participating in the program and contamination across those worksites cannot be avoided.
Employee-level inclusion criteria:
- 18 years or older
- Willing to provide informed consent
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Stand & Move at Work+ Stand & Move at Work+ This arm will receive access to the same web-based platform and toolkit as the other arm. Additionally, worksites in this arm will be assigned and expert facilitator who will meet regularly with the worksite Champions to assist with implementation. Stand & Move at Work Stand & Move at Work Given an evidence-based workplace program to reduce sedentary behavior and increase standing and moving using a web-based platform. The web platform has a toolkit with strategies and guides for the worksite Champions to address changes at the environmental, social, and cultural levels.
- Primary Outcome Measures
Name Time Method Changes in posture Baseline, 3 month, 12 months, and 24 months Accelerometer-based (activPAL) sensor fixed to the thigh that measures sitting, standing, and lying down over 7 days.
Intervention Fidelity 24 months A questionnaire-based assessment of intervention fidelity completed by study participants regarding the advocates (competence and adherence) through an online portal. SCORING RANGE
Researcher derived measures of fidelity 24 months A single composite measure of directly-observed intervention delivery assessed via web analytics, participation rates, and other calculated measures of fidelity.
Competence/Adherence 24 months A questionnaire-based assessment of intervention fidelity completed by study champions (competence and adherence) through an online portal. Based on Likert-scales and interval scales. SCORING RANGE
- Secondary Outcome Measures
Name Time Method Comparison of program-related costs Baseline, 3 month, 12 months, and 24 months. Program-related costs above and beyond cost of sit-stand workstation which may include advocate time spent implementing the intervention and intervention supplies.
Change in health-related quality of life Baseline, 3 month, 12 months, and 24 months. 36-Item Short Form Survey (SF36) assesses quality of life that will be used to estimate incremental cost effectiveness. Scored from 0 to 100, with 0 being maximum disability and 100 being no disability.
Change in musculoskeletal pain Baseline, 3 months, 12 months, and 24 months. The Nordic Musculoskeletal Questionnaire (NMQ) assesses pain by bodily region on a Likert-type scale SCORING RANGE.
Change in Work Productivity and Activity Impairment Questionnaire - General Health Baseline, 3 months, 12 months, and 24 months. Work Productivity and Activity Impairment Questionnaire: General Health (WPAI:GH) assesses impairment in paid work and activities in the preceding 7 days on an interval and Likert-type scale with a higher score indicating greater impariment.
Trial Locations
- Locations (1)
Arizona State University College of Health Solutions
🇺🇸Phoenix, Arizona, United States