Effects of Aerobic Exercise on Occupational Burnout

Sponsor
University Hospital, Basel, Switzerland (Other)
Overall Status
Completed
CT.gov ID
NCT01575743
Collaborator
(none)
24
1
2
48
0.5

Study Details

Study Description

Brief Summary

The aim of the present study is to investigate the impact of regular aerobic exercise on psychopathology, cortisol secretion, BDNF, sleep, cognitive performance, and psychological functioning in people suffering from professional burnout. Pre- and postassessments after 12 weeks of training will be performed.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: aerobic exercising
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
24 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Aerobic Exercise on Occupational Burnout
Study Start Date :
Mar 1, 2008
Actual Primary Completion Date :
Feb 1, 2012
Actual Study Completion Date :
Mar 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Aerobic Exercise

Behavioral: aerobic exercising
All participants take part in an aerobic exercise training program with a total weekly energy expenditure of 17.5 kcal/kg/week over the entire 12-week intervention period. The dose of exercise is determined using exercise prescription guidelines established by the American College of Sports Medicine (ACSM, American College of Sports Medicine, 2000). All trainings take place at a local public gym under supervision of previously trained exercise coaches from the Institute of Exercise and Health Sciences of the University Basel. Participants can choose between different training devices for cardiovascular training. Energy expenditure is assessed using the values of burned calories provided by the training devices based on age, weight and training performance. Heart rate is monitored during all training sessions with chest belt heart rate monitors (PolarĀ®) to ensure training below the anaerobic threshold with heart rates between 60 - 75 % of the maximum heart rate.

Other: healthy controls

Behavioral: aerobic exercising
All participants take part in an aerobic exercise training program with a total weekly energy expenditure of 17.5 kcal/kg/week over the entire 12-week intervention period. The dose of exercise is determined using exercise prescription guidelines established by the American College of Sports Medicine (ACSM, American College of Sports Medicine, 2000). All trainings take place at a local public gym under supervision of previously trained exercise coaches from the Institute of Exercise and Health Sciences of the University Basel. Participants can choose between different training devices for cardiovascular training. Energy expenditure is assessed using the values of burned calories provided by the training devices based on age, weight and training performance. Heart rate is monitored during all training sessions with chest belt heart rate monitors (PolarĀ®) to ensure training below the anaerobic threshold with heart rates between 60 - 75 % of the maximum heart rate.

Outcome Measures

Primary Outcome Measures

  1. Change of burnout severity by aerobic exercise training [Change from baseline to follow-up after 12 weeks]

    burnout severity measured by psychopathology, cortisol secretion, BDNF, sleep, cognitive performance, and psychological functioning

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • burnout

  • male participants

  • non-smokers

Exclusion Criteria:
  • psychiatric disorders

  • smokers

  • physical diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 UPK Basel Basel Switzerland 4012

Sponsors and Collaborators

  • University Hospital, Basel, Switzerland

Investigators

  • Principal Investigator: Johannes Beck, MD, UPK Basel, Basel Switzerland

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Basel, Switzerland
ClinicalTrials.gov Identifier:
NCT01575743
Other Study ID Numbers:
  • Burnout_1
First Posted:
Apr 11, 2012
Last Update Posted:
Apr 11, 2012
Last Verified:
Apr 1, 2012
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 11, 2012