None listed
Conditions
Interventions
Participants will be randomised to complete either progressive resistance training or graded aerobic training for 4 weeks.
Sponsors
Austin Health
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
10 Years to 18 Years
Healthy volunteers
No
Inclusion criteria
Must have CFS.
Exclusion criteria
Any pyschological condition or suffer from asthma or any other respiratory disorders.
Outcome results
None listed