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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01759927
Other study ID # S54788
Secondary ID
Status Completed
Phase N/A
First received December 30, 2012
Last updated December 2, 2015
Start date February 2013
Est. completion date March 2015

Study information

Verified date December 2015
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Interventional

Clinical Trial Summary

The primary aim of this study is to investigate if and how a physical activity counselor can offer an added value in exercise promotion in physically inactive employees. We will explore if the physical activity counselor in the workplace setting can motivate sedentary employees to engage into systematic participation in sports and/or exercise by means of a short term coaching of 12 weeks. We aim to include 300 employees in the physical activity coaching process.


Description:

Being physically active on a regular basis has many health benefits. Nevertheless, the majority of the Belgian population doesn't reach the recommended amount and intensity of physical activity to profit from these health benefits. A physical activity counselor can possibly play a crucial role for these physically inactive individuals. He/she can design an individualized exercise program to stimulate the person to become lifelong physical active. Research has shown that exercise promotion at work can result in a lower absenteeism, prevention of burn-out and a positive corporate identity.


Recruitment information / eligibility

Status Completed
Enrollment 301
Est. completion date March 2015
Est. primary completion date January 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Employee of Janssen Pharmaceutics Belgium

- Physically inactive lifestyle (not reaching 150 minutes of moderate-to-vigorous physical activity a week)

- PAR-Q questionnaire all answers negative, if one or more answers are positive a permission of a physician is necessary

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
physical activity coaching
After measuring physical actity, physical fitness level, anthropometric and psychosocial variables a personalized 12 week physical activity program is made (=baseline). The intervention consisted of two face-to-face counselling sessions at the start of the intervention, short contacts by e-mail or telephone at weeks 3, 6 and 9, and two face-to-face counselling sessions at the end of the intervention. Employees exercise on their own. After 12 weeks and 6 months all measures are repeated.

Locations

Country Name City State
Belgium Katholieke Universiteit Leuven - Faculty of Kinesiology and Rehabilitation Sciences Leuven Vlaams Brabant

Sponsors (2)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven Janssen Pharmaceutica

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in psycho-social variables Measuring general and work related well-being, motivation to be physically active and social identification with the physical activity group baseline, 12 weeks, 6 months No
Primary Change in objective measure of degree of physical activity Sensewear: accelerometer worn on the upper arm during 7 consecutive days measuring the physical activity pattern during this period baseline, 12 weeks, 6 months No
Secondary Change in health-related anthropometric measures Weight, Abdominal circumference, Bodycomposition (fat- and musclepercentage) baseline, 12 weeks, 6 months No
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