Interventions to Increase Workplace Wellness

Sponsor
University of British Columbia (Other)
Overall Status
Completed
CT.gov ID
NCT02535754
Collaborator
Canadian Cancer Society (CCS) (Other)
682
1
3
47
14.5

Study Details

Study Description

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).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: ALIVE
  • Behavioral: CCS BCY
  • Behavioral: ALIVE + CCS BCY
N/A

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
Actual Enrollment :
682 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Interventions to Increase Workplace Wellness
Study Start Date :
Apr 1, 2010
Actual Primary Completion Date :
Mar 1, 2013
Actual Study Completion Date :
Mar 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: ALIVE

Email program N=170

Behavioral: ALIVE
The company assigned to this condition offered employees participation in the ALIVE program. This program was validated in a previous worksite-based randomized controlled trial (RCT). A baseline assessment includes questions asking about: presence of children at home, habits related to cooking and eating out, physical activity preferences, stage of readiness of change, and perceived barriers to achieving heath behavior goals. This information provides the basis for immediate feedback and individually-tailored messages that include goal-setting and tips to achieve these goals, interactive features, and health information. Biweekly messages are sent for a total of 48 weeks. Outcome data were based on all individuals who completed the baseline assessment.

Experimental: CCS BCY

Comprehensive program N=285

Behavioral: CCS BCY
The company assigned to this condition participated in a comprehensive year-long workplace wellness program intervention focusing on nutrition, weight control, and physical activity, led by the CCS BCY. The program was modeled after a previous successful CCS BCY tobacco control worksite program. This program stresses the importance of developing social and environmental supports at the worksite to promote behavior change . Such supports could include food availability (e.g., cafeteria and vending machine selections), the built environment (e.g., availability of bike racks); social environment (e.g., group lunchtime walking clubs), and health communications (e.g., company newsletters). Outcome data were based on all individuals who completed the baseline assessment.

Experimental: ALIVE + CCS BCY

Email + comprehensive program N=225

Behavioral: ALIVE + CCS BCY
The company assigned to this condition received both the ALIVE and CCS BCY programs. Employees were encouraged to take part in both ALIVE and company initiatives, but participation in these activities was based on individual preference. Outcome data were based on all individuals who completed the baseline assessment.

Outcome Measures

Primary Outcome Measures

  1. Change in number of fruit and vegetable servings per day [16 months]

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

Secondary Outcome Measures

  1. Absenteeism (days) [16 months]

    Self-reported absenteeism at baseline and 16 months

  2. Change in body weight (lbs) [16 months]

    Self-reported height and weight at baseline and 16 months

  3. Physical activity efficacy (minutes) [16 months]

    Self-reported efficacy for physical activity at baseline and 16 months

  4. Participant perspectives on the program (theme) [16 months]

    Focus groups identified participant responses to the program including strengths and weaknesses.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of British Columbia Vancouver British Columbia Canada V6T1Z3

Sponsors and Collaborators

  • University of British Columbia
  • Canadian Cancer Society (CCS)

Investigators

  • Principal Investigator: Carolyn C Gotay, PhD, University of British Columbia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of British Columbia
ClinicalTrials.gov Identifier:
NCT02535754
Other Study ID Numbers:
  • H10-01079
First Posted:
Aug 31, 2015
Last Update Posted:
Aug 31, 2015
Last Verified:
Aug 1, 2015

Study Results

No Results Posted as of Aug 31, 2015