Health Promotion Intervention Program at the Workplace

This study is currently recruiting participants. (see Contacts and Locations)
Verified December 2013 by Wingate Institute
Sponsor:
Information provided by (Responsible Party):
Wingate Institute
ClinicalTrials.gov Identifier:
NCT01628419
First received: June 21, 2012
Last updated: December 23, 2013
Last verified: December 2013
  Purpose

The purpose of the current investigation is to examine the effects of health intervention program at the workplace on health risks for cardiovascular disease, well-being and absenteeism at the workplace.

Participants: 1500 male and female employees from 10 different companies across Israel will take part in the study. Age: older than 18 yrs.

Hypothesis 1: The intervention program will have positive effects on the health risks for cardiovascular disease. For example: Will be reflected in a decrease in LDL and increase in HDL.

Hypothesis 2: The intervention program will have positive effects on the absenteeism at the workplace (e.g. decrease in days of sick leave per employee).


Condition Intervention
Conditions Influencing Health Status
Behavioral: Health intervention

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Health Services Research
Official Title: Health Promotion Intervention Program at the Workplace

Resource links provided by NLM:


Further study details as provided by Wingate Institute:

Primary Outcome Measures:
  • Anthropometric measures [ Time Frame: 6 months ] [ Designated as safety issue: No ]
    The following measures will be evaluated: Height and body mass (Kg) and Body mass index will be calculated (BMI), hip and waist circumference and the ratio between the two measures will be calculated.


Secondary Outcome Measures:
  • Absenteeism from work [ Time Frame: 6 months ] [ Designated as safety issue: No ]
    Number days of sick leave each employee had during the 6 months period.

  • Blood tests results [ Time Frame: 6 months ] [ Designated as safety issue: No ]
    Improvement in Blood test results: blood glucose levels and Hemuglubin A1c, Hemoglubin, lipid profile (LDL, HDL, cholestrol, Triglycerides), liver function (ALT, GGT)


Estimated Enrollment: 1500
Study Start Date: July 2012
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Health intervention program
Health promotion intervention program will be implemented at each workplace and will include: exercise program, nutritional counseling for the kitchen service, lectures on different topics (physical activity, nutrition, sleeping behaviour etc.).
Behavioral: Health intervention

physical activity program at the workplace - once a week with a certified trainer. (The program will include: aerobic exercises as well as resistance exercises). The employees will encourage to perform two additional workouts during the week.

Nutritional counseling for the kitchen staff Lectures - lectures will be given at each worksite on different topics: physical activity, nutrition, sleeping behaviour, mental aspects.


  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • agreement to participate in the study,
  • older than 18 yrs

Exclusion Criteria:

  • Missing blood tests results and anthropometric measures prior to the beginning of the study,
  • unstable cardiac disease,
  • unstable hypertension during rest (above 200 mmHg systolic blood pressure and above 110 mmHg of diastolic blood pressure),
  • pregnancy,
  • using pacemaker,
  • past cardiac incidence during the 6 months preceding the test,
  • other disease that might cause contraindication for exercise
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01628419

Contacts
Contact: Eyal Shargal, PhD +972-9-8639418 eyals@wingate.org.il
Contact: Rotem Cohen, MSc +972-9-8639404 rotemc@wingate.org.il

Locations
Israel
Wingate Institute Recruiting
Netanya, Israel
Contact: Eyal Shargal, PhD    +972-9-8639418    eyals@wingate.org.il   
Contact: Rotem Cohen, MSc    +972-98639404    rotemc@wingate.org.il   
Principal Investigator: Eyal Shargal, PhD         
Sponsors and Collaborators
Wingate Institute
Investigators
Study Director: Eyal Shargal, PhD Wingate Institute, Israel
  More Information

No publications provided

Responsible Party: Wingate Institute
ClinicalTrials.gov Identifier: NCT01628419     History of Changes
Other Study ID Numbers: WIN12345
Study First Received: June 21, 2012
Last Updated: December 23, 2013
Health Authority: Israel: Ministry of Health

Keywords provided by Wingate Institute:
Health promotion
Intervention
Workplace
Exercise program

ClinicalTrials.gov processed this record on July 22, 2014