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Clinical Trials/NCT02535754
NCT02535754CompletedNot Applicable

Interventions to Increase Workplace Wellness

University of British Columbia1 site in 1 country682 target enrollmentStarted: April 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
682
Locations
1
Primary Endpoint
Change in number of fruit and vegetable servings per day

Study Overview

Brief Summary

Behaviour changes such as improving nutrition, increasing physical activity, and decreasing obesity are linked with lower mortality and morbidity and fewer cancers. Health promotion programs in the workplace are a promising way to reach a large segment of the population. This project evaluated the efficacy of three approaches - all of which were based on previous research and programs with demonstrated positive benefits - on cancer-related outcomes (healthy eating, physical activity, normal body weight) and work-related outcomes (absenteeism, presenteeism).

Detailed Description

The project evaluated the efficacy of three health promotion interventions on cancer- and work-related outcomes. Three worksites in British Columbia were randomly assigned to one of three conditions: (1) an empirically-validated intervention directed at individual behavior change using personally-tailored messages delivered by email (ALIVE) ; (2) a comprehensive approach building on social and institutional support developed by the Canadian Cancer Society British Columbia Yukon and previously used for worksite tobacco control (CCS BCY) and (3) an intervention including both of these approaches (CCS BCY + ALIVE). The primary outcome was change in fruit and vegetable consumption from baseline to 16 months, as an indicator of healthy diet. Change in weight, physical activity, and work productivity were secondary outcomes. The investigators also conducted focus groups to assess participant perspectives on the programs which comprise another secondary outcome.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Employee of the company
  • •English speaking with reading level at Flesch-Kincaid 8.5 grade level
  • •Ability to provide access to individual work email address

Exclusion Criteria

  • •Non-English speaking without reading level at Flesch-Kincaid 8.5 grade level
  • •Inability to provide access to individual work email address

Arms & Interventions

ALIVE

Experimental

Email program N=170

Intervention: ALIVE (Behavioral)

CCS BCY

Experimental

Comprehensive program N=285

Intervention: CCS BCY (Behavioral)

ALIVE + CCS BCY

Experimental

Email + comprehensive program N=225

Intervention: ALIVE + CCS BCY (Behavioral)

Outcomes

Primary Outcomes

Change in number of fruit and vegetable servings per day

Time Frame: 16 months

Self-reported number of fruit and vegetable servings at baseline and 16 months

Secondary Outcomes

  • Absenteeism (days)(16 months)
  • Change in body weight (lbs)(16 months)
  • Physical activity efficacy (minutes)(16 months)
  • Participant perspectives on the program (theme)(16 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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