Stand & Move at Work II: Effectiveness and Implementation of a Worksite Wellness Program
ConditionSedentary Behavior
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorArizona State University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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.
Disqualifiers
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.
18 years or older
Trial design
Design model
Parallel
Treatments tested in this trial
Stand & Move at Work
BehavioralWeb-based platform only.
Stand & Move at Work+
BehavioralWeb-based platform and support from an expert facilitator
Treatment groups
4,800 Participants
are divided into 2 treatment groupsGroup A: Stand & Move at WorkActive comparator 1 intervention
Group B: Stand & Move at Work+Experimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Changes in posture
Accelerometer-based (activPAL) sensor fixed to the thigh that measures sitting, standing, and lying down over 7 days.
Time frame
Baseline, 3 month, 12 months, and 24 months2
Competence/Adherence
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
Time frame
3 months3
Competence/Adherence
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
Time frame
12 months4
Competence/Adherence
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
Time frame
24 monthsSecondary outcomes
1
Comparison of program-related costs
Program-related costs above and beyond cost of sit-stand workstation which may include advocate time spent implementing the intervention and intervention supplies.
Time frame
Baseline, 3 month, 12 months, and 24 months.2
Change in health-related quality of life
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.
Time frame
Baseline, 3 month, 12 months, and 24 months.3
Change in musculoskeletal pain
The Nordic Musculoskeletal Questionnaire (NMQ) assesses pain by bodily region on a Likert-type scale SCORING RANGE.
Time frame
Baseline, 3 months, 12 months, and 24 months.4
Change in Work Productivity and Activity Impairment Questionnaire - General Health
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.
Time frame
Baseline, 3 months, 12 months, and 24 months.Other outcomes
1
Change in sedentary behavior
Sedentary behavior questionnaire (SBQ) is a brief questionnaire to assess time spent sitting in different work and non-work contexts SCORING RANGE
Time frame
Baseline, 3 month, 12 months, and 24 months.Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Arizona State University
Lead sponsor
National Cancer Institute (NCI)
Collaborator
University of Minnesota
Collaborator
The University of Queensland
Collaborator
University of Nebraska
Collaborator
University of Utah
Collaborator
University of Virginia
Collaborator
Source ClinicalTrials.gov