About this trial
This randomized, controlled, five-arm, parallel-group trial will evaluate the effects of 8 weeks of supervised resistance training and developmental position-based exercise, with or without real-time non-invasive intra-abdominal pressure biofeedback, in adults aged 40 to 60 years with chronic low back pain. The trial will compare supervised gym-based agonist-antagonist paired set resistance training with OHMTRACK, supervised gym-based resistance training without OHMTRACK, supervised physiotherapy-based developmental exercise with OHMTRACK, home-based developmental exercise with OHMTRACK, and an active control condition. Primary outcomes will assess changes in pain and physical function after the intervention. Secondary outcomes will include neuromuscular coordination, postural stabilization, cardiovascular, respiratory, metabolic, behavioral, feasibility, and follow-up outcomes.
Eligibility criteria
Qualifiers
Chronic low back pain lasting more than 12 weeks, with current low back pain at screening/baseline.
Resting blood pressure below 139/89 mmHg.
Health status allowing participation in moderate-intensity resistance training and aerobic activity.
Physically active, but not professional athletes.
Disqualifiers
Absolute or relative contraindications to resistance training or other clinically relevant cardiovascular contraindications.
Coronary artery disease, heart rhythm disorders, acute myocarditis, Marfan syndrome, or other cardiovascular conditions judged unsafe by the study physician.
History of myocardial infarction, cerebrovascular disease, peripheral vascular disease, or grade II-IV hypertension.
Type 1 or type 2 diabetes mellitus.
Trial design
Treatments tested in this trial
- Gym settings
- Physio settings
- Home - based settings: exercises based on developmental positions
- Home - based settings: Usual activity monitoring
Treatment groups
Sponsors and collaborators
Charles University, Czech Republic
Lead sponsor
The Jerzy Kukuczka Academy of Physical Education in Katowice
Collaborator