- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04723797
The Effect of a Physical Activity Program on Burnout Risk Among Secondary School Teachers
January 20, 2021 updated by: Luna Coffyn, Vrije Universiteit Brussel
The Effect of a Physical Activity Program on Burnout Risk Among Secondary School: a Randomised Controlled Trial
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.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
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 Type
Interventional
Enrollment (Anticipated)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Brussel, Belgium, 1000
- Recruiting
- Vrije Universiteit Brussel
-
Contact:
- Luna Coffyn, Master
- Phone Number: +32491331597
- Email: luna.christel.coffyn@vub.be
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / 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.
|
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.
|
Physical activity program consisting of running and/or cycling
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Burnout risk
Time Frame: 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.
|
9 weeks
|
|
Recovery need
Time Frame: 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.
|
9 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
School and teaching subjects
Time Frame: 9 weeks
|
It is a self-designed questionnaire about location and type of school, grades and teaching subjects
|
9 weeks
|
|
Rate of perceived exertion
Time Frame: 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.
|
9 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
February 15, 2021
Primary Completion (ANTICIPATED)
April 4, 2021
Study Completion (ANTICIPATED)
April 25, 2021
Study Registration Dates
First Submitted
January 15, 2021
First Submitted That Met QC Criteria
January 20, 2021
First Posted (ACTUAL)
January 26, 2021
Study Record Updates
Last Update Posted (ACTUAL)
January 26, 2021
Last Update Submitted That Met QC Criteria
January 20, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- B.U.N. 1432020000307
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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