????????????? ????? ?? ?????? ???? ??????????. Low back pain
Conditions
Interventions
Intervention 1: Intervention group 1: The group receiving dynamic neuromuscular training combined with virtual reality technology. Participants receive Dynamic Neuromuscular Stabilization exercises co
the chosen VR game (Dodgeball) is selected based on prior literature for this population. Intervention 2: Intervention group 2:The group receiving dynamic neuromuscular training without the use of vir
Sponsors
The University of Shahid Beheshti
Eligibility
Sex/Gender
Female
Age
30 Years to 50 Years
Inclusion criteria
Inclusion criteria: Women between 30-50 years of age Lumbar lordosis greater than 40 degrees Body-mass index (BMI) between 18.5 and 27 Pain intensity between 3 and 7 on the Visual Analogue Scale (VAS)
Exclusion criteria
Exclusion criteria: history of spinal fractures, surgery, or joint disease Use of orthotic insoles, a cane, antidepressant or narcotic medications, or muscle relaxants within 30 days prior to the study, and no significant visual impairment or motor disorders that would prevent the use of virtual-reality equipment Presence of pathological signs related to the condition, such as heart disease, cancer, tumors, previous surgery, etc. Presence of orthopedic deformities or neurosurgical diseases Presence of disc degeneration or other conditions that could influence the interpretation of the results (e.g., severe fibromyalgia or rheumatoid arthritis in combination with other treatments) Surgery or pregnancy within the past 30 days Use of devices or apparatuses for treating hyper-lordosis Presence of any other postural abnormalities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hyperlordosis. Timepoint: Outcome assessments will be conducted at baseline and after the completion of the 6-week intervention period. Method of measurement: Hyperlordosis will be assessed using the Spinal Mouse device.;Pain intensity. Timepoint: Outcome assessment will be conducted at baseline and after the completion of the 6-week intervention period. Method of measurement: Pain intensity will be measured using the Visual Analogue. | — |
Secondary
| Measure | Time frame |
|---|---|
| Static balance. Timepoint: Outcome assessment will be conducted at baseline and after the completion of the 6-week intervention period. Method of measurement: static Balance will be assessed using the Biodex Balance System.;Dynamic balance. Timepoint: Outcome assessment will be conducted at baseline and after the completion of the 6-week intervention period. Method of measurement: Dynamic Balance will be assessed using the Biodex Balance System.;Lumbar proprioception. Timepoint: Outcome assessment will be conducted at baseline and after the completion of the 6-week intervention period. Method of measurement: Lumbar Proprioception will be measured using a goniometer.;Range of motion. Timepoint: Outcome assessment will be conducted at baseline and after the completion of the 6-week intervention period. Method of measurement: Range of motion will be measured using the MobeeMed device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNiusha Tashakori
The University of Shahid Beheshti
Outcome results
None listed