Status:

UNKNOWN

Working on Wellness (WOW) Intervention

Lead Sponsor:

University of Cape Town

Collaborating Sponsors:

VU University of Amsterdam

Conditions:

Physical Activity

Eligibility:

All Genders

21-65 years

Phase:

NA

Brief Summary

The main aim of this study is to measure the effectiveness of a worksite health promotion programme on improving physical activity behaviour and associated biological risk factors for cardiovascular d...

Detailed Description

Study Design: "Working on Wellness - WOW" is a randomised controlled trial in South African worksites with a 12 month follow-up. Randomisation will take place at the company level, where participatin...

Eligibility Criteria

Inclusion

  • Employees identified to be at 'increased' or 'high' risk for CVD are eligible to take part in the research study. Risk status will be determined by using the (Euro) SCORE 12, together with their habitual physical activity levels, and Body Mass Index. SCORE incorporates age, total cholesterol, blood pressure and smoking status. This score ranks individuals according to their level of risk, ranging from very low to very high 10-year risk of fatal CVD (Appendix 1). Those with a risk of 5% or higher will be considered eligible.
  • Independent of the risk score, employees who are inactive (i.e., who do not comply with at least 30 minutes of moderate to vigorous activity on at least 5 days per week), or who smoke, and employees who are overweight (i.e., Body Mass Index ≥ 25 kg/m2) also will be eligible to take part in the study. Other inclusion criteria include being older than 18 years and having a contract with employer until end of 12-month measurement period

Exclusion

  • Employees will be excluded for the following reasons: pregnancy, diagnosis or treatment of cancer, any other disorder that makes physical activity impossible. Contract workers whose employ with the company will end before the 12 month follow up measurement, will also be excluded from the study.

Key Trial Info

Start Date :

November 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2012

Estimated Enrollment :

800 Patients enrolled

Trial Details

Trial ID

NCT01494207

Start Date

November 1 2009

End Date

June 1 2012

Last Update

February 27 2012

Active Locations (1)

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1

University of Cape Town

Cape Town, South Africa, 7725