Investigation of the Effects of Lumbopelvic Movement Training on Different Parameters in Healthy Sedentary Individuals
NCT ID: NCT07019376
Last Updated: 2025-12-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
48 participants
INTERVENTIONAL
2025-06-04
2025-11-30
Brief Summary
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Detailed Description
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The pelvis makes sinusoidal up-down movements in the frontal and sagittal planes and rotational movements in the transverse plane during walking. These movements are provided by the local and global muscles surrounding the pelvis and hip joint. The reduction of pelvic oscillations in the normal gait pattern may lead to decreased energy expenditure and increased muscle force production.
Lumbopelvic proprioception plays an important role in providing neuromuscular control, creating effective movement, providing coordination, revealing muscle activation at the appropriate timing, preventing spinal and lower extremity injuries and reducing lumbar pain. Decreased proprioceptive sensation leads to impaired movement of the lumbopelvic region and lower and upper extremities, as well as pain and injuries.
In case of weakening of lumbopelvic neuromuscular control and spinal proprioception, significant losses in balance and muscle strength and endurance occur. In order to gain proprioception, balance and strength-endurance parameters should be focused on, and in order to gain balance and strength-endurance parameters, proprioception sense should be developed.
In this direction, the investigators think that lumbopelvic movement training accompanied by visual biofeedback will have a direct effect on pelvic oscillations, lumbar, lumbopelvic, hip and knee proprioception, lower extremity balance and core muscle endurance and these effects will be reflected on the health parameters and daily living activities of individuals. For this purpose, the investigators aim to evaluate the effects of lumbopelvic movement training. At the same time, as a result of the literature review, it is aimed to eliminate the deficiency in this field.
Conditions
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Keywords
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Study Design
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RANDOMIZED
FACTORIAL
DIAGNOSTIC
SINGLE
Study Groups
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Visual biofeedback supported group
participants will perform lumbopelvic exercises for 8 weeks, 2 sessions per week for 8 weeks by providing visual biofeedback with a laser.
Visual biofeedback supported lumbopelvic movement training
6 exercises that provide movement of the lumbopelvic region will be performed for 8 weeks and 2 times each week. The exercises will be followed visually with the help of a laser.
Visual biofeedback unsupported group
Participants will perform lumbopelvic exercises for 8 weeks, 2 sessions per week, without any biofeedback support.
visual biofeedback unsupported lumbopelvic movement training
6 exercises that provide movement of the lumbopelvic region will be performed for 8 weeks and 2 times each week. The exercises will be the same exercises as the group with laser support, but no visual support will be provided.
Control Group
control group not receiving any exercise
No interventions assigned to this group
Interventions
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Visual biofeedback supported lumbopelvic movement training
6 exercises that provide movement of the lumbopelvic region will be performed for 8 weeks and 2 times each week. The exercises will be followed visually with the help of a laser.
visual biofeedback unsupported lumbopelvic movement training
6 exercises that provide movement of the lumbopelvic region will be performed for 8 weeks and 2 times each week. The exercises will be the same exercises as the group with laser support, but no visual support will be provided.
Eligibility Criteria
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Inclusion Criteria
* individuals without any spine or hip pain problems
* individuals who have not undergone any spine or hip surgery
* individuals who volunteered to participate in the study
Exclusion Criteria
* individuals with any spine or hip pain problems
* individuals who have undergone any spine or hip surgery
* individuals who did not volunteered to participate in the study
18 Years
35 Years
ALL
Yes
Sponsors
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Gazi University
OTHER
Responsible Party
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Fırat Kara
Principal Investigator
Principal Investigators
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Fırat Kara, Phd Student
Role: PRINCIPAL_INVESTIGATOR
Nuh Naci Yazgan University
Locations
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Nuh Naci Yazgan University
Kayseri, Kocasinan, Turkey (Türkiye)
Countries
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Other Identifiers
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GAZIU-FTR-FK-001
Identifier Type: -
Identifier Source: org_study_id