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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04723797
Other study ID # B.U.N. 1432020000307
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 15, 2021
Est. completion date April 25, 2021

Study information

Verified date January 2021
Source Vrije Universiteit Brussel
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the effect of a 6 weeks physical activity program on burnout risk in secondary school teachers. Also, the difference between the effects of moderate en vigorous-intensity physical activity will be investigated.


Description:

Given the increased risk of burnout among secondary school teachers, effective interventions are needed. Physical activity may play a big role in preventing and/or reducing burnout. Therefore the purpose of this research is to investigate the effect of physical activity on the risk of burnout in secondary school teachers. The participants in the intervention group will be asked to perform a specific physical activity program (including running and/or cycling at a moderate or vigorous intensity) for 6 weeks. The control group will be asked to keep their lifestyle as it was prior to the study. To assess the effect of this activity program, the participants will have to fill in a questionnaire at three time points. Lastly, the participants have to fill in an activity diary every day, enabling to assess intervention adherence.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date April 25, 2021
Est. primary completion date April 4, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria: - Participants who are not meeting the guidelines for physical activity. - Participants who are willing to run or cycle. Exclusion Criteria: - Participants who are not speaking the Dutch language. - Participants unable or unwilling to give informed consent. - Participants who are not able to be physically active, due to injuries, physical disabilities, etc. - Participants who already met the guidelines for physical activity. - Participants who are following a diet. - Participants who have been following psychological treatment in the past 6 months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Physical activity
Physical activity program consisting of running and/or cycling

Locations

Country Name City State
Belgium Vrije Universiteit Brussel Brussel

Sponsors (1)

Lead Sponsor Collaborator
Vrije Universiteit Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Burnout risk Assessing the burnout risk by using the Burnout assessment tool (BAT). It consist 34 items scored on a 5-Point likert scale ranging from 1 (never) to 5 always. The greater the total score, the more the participant is in risk of a burnout. 9 weeks
Primary Recovery need Assessing the recovery need by using the Short Inventory to Monitor Psychosocial. hazards (SIMPH). This survey consists of 5 questions with the answer options 'yes' or no'. A score of 3 times 'yes' out of 5, is an indication of a possible increased need for recovery at work. 9 weeks
Secondary School and teaching subjects It is a self-designed questionnaire about location and type of school, grades and teaching subjects 9 weeks
Secondary Rate of perceived exertion Effort and exertion will be measured by using the Borg Rating of Perceived Exertion scale. The borg scale ranges from '6' to '20' and is highly correlated with the heart rate. A borg scale of 10 corresponds to a heart rate of 100bpm in a healthy adult. 9 weeks
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