Non-specific low back pain. Dorsalgia, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Having pain (2-5 based on the var scale) The gender of men and women in the age range of 40-60 Chronic back pain for more than three months The ability to do exercises (based on the opinion of a specialist doctor) Voluntary participation in the study
Exclusion criteria
Exclusion criteria: History of spondylolisthesis rheumatic inflammatory diseases acute disc herniation had any spinal surgery irregular participation in training sessions (3 consecutive sessions - 5 alternating sessions) failure to complete research tests any unpredictable problems that hinder The subject's presence in the training withdrawal will be voluntary
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Low back pain. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: Pain assessment with VAS scale, fear of movement assessment with Tempa scale, quality of life assessment with SF36 test, functional disability assessment with ODI index, strength assessment with digital dynamometer, endurance assessment with McGill test, back flexibility assessment with Schuber test, motor performance assessment With Lomajuki test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Gait Performance. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: With foot scan device.;Pain intensity. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: Pain assessment with Vas scale.;Fear of movement. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: fear of movement assessment with Tempa scale.;Quality of life. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: quality of life assessment with SF36.;Functional disability. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: functional disability assessment with ODI index.;Core muscle strength. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention > 2. Post-intervention – immediately after completing the 8-week reactive–core stability exercise program. Method of measurement: strength assessment with digital dynamometer.;Muscular endurance. Timepoint: Outcome variables will be measured at two timepoints: > 1. Baseline – prior to the start of the intervention | — |
Countries
Iran (Islamic Republic of)
Contacts
Isfehan Univercity