The Effect of a Physical Activity Program on Burnout Risk Among Secondary School Teachers

Sponsor
Vrije Universiteit Brussel (Other)
Overall Status
Recruiting
CT.gov ID
NCT04723797
Collaborator
(none)
70
1
3
2.3
30.9

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Physical activity
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized control trial with a control group, a moderate-intensity intervention group, and a high-intensity intervention groupRandomized control trial with a control group, a moderate-intensity intervention group, and a high-intensity intervention group
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
The Effect of a Physical Activity Program on Burnout Risk Among Secondary School: a Randomised Controlled Trial
Anticipated Study Start Date :
Feb 15, 2021
Anticipated Primary Completion Date :
Apr 4, 2021
Anticipated Study Completion Date :
Apr 25, 2021

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

The participants in the control group will be asked to maintain their lifestyle as before the study.

Experimental: Moderate-intensity group

Participants will be asked to perform a physical activity program, consisting of cycling and/or running for 6 weeks of at least 150min/week. This at a moderate intensity, which means a slightly increased heart rate and breathing also talking is possible.

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

Experimental: Vigorous-intensity group

Participants will be asked to perform a physical activity program, consisting of cycling and/or running for 6 weeks of at least 75min/week. This at a vigorous intensity, which means increased heart rate and breathing also talking is possible.

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

Outcome Measures

Primary Outcome Measures

  1. Burnout risk [9 weeks]

    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.

  2. Recovery need [9 weeks]

    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.

Secondary Outcome Measures

  1. School and teaching subjects [9 weeks]

    It is a self-designed questionnaire about location and type of school, grades and teaching subjects

  2. Rate of perceived exertion [9 weeks]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vrije Universiteit Brussel Brussel Belgium 1000

Sponsors and Collaborators

  • Vrije Universiteit Brussel

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Luna Coffyn, Master student, Vrije Universiteit Brussel
ClinicalTrials.gov Identifier:
NCT04723797
Other Study ID Numbers:
  • B.U.N. 1432020000307
First Posted:
Jan 26, 2021
Last Update Posted:
Jan 26, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 26, 2021