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

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

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.

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

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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