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

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-04

Study Completion Date

2025-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study was to investigate the effects of visual biofeedback-assisted lumbopelvic movement training on pelvic proprioception, pelvic oscillation, lower extremity static and dynamic balance and core muscle endurance in sedentary healthy individuals.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The lumbopelvic region is an anatomical region where the lumbar spine and pelvis move in harmony in terms of timing and intensity, called the lumbopelvic rhythm, which requires the static, dynamic and neural system to work together, formed by local and global muscles, osteoligamentous structures and neural control. It acts as a force bridge between the lower and upper extremities. Pain, disability, limited activations, atrophy and especially decreases in motor control and proprioception can negatively affect the rhythm and stabilisation in the region. Exercises that contribute to the movement and stabilisation of the lumbopelvic region. There are studies showing that it re-facilitates synaptogenesis, synaptic potentials and reorganisation in areas represented by movement in the motor cortex.

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

See the medical conditions and disease areas that this research is targeting or investigating.

Exercise Training

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

proprioception biofeedback lumbopelvic exercise pelvic sway balance endurance

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Total of 3 groups including the control group who did not receive any training
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

Group Type ACTIVE_COMPARATOR

Visual biofeedback supported lumbopelvic movement training

Intervention Type OTHER

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.

Group Type ACTIVE_COMPARATOR

visual biofeedback unsupported lumbopelvic movement training

Intervention Type OTHER

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

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.

Intervention Type OTHER

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.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* sedentary individuals who are not interested in any sport
* 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

* athlete individuals who are interested in any sport
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Gazi University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Fırat Kara

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Fırat Kara, Phd Student

Role: PRINCIPAL_INVESTIGATOR

Nuh Naci Yazgan University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Nuh Naci Yazgan University

Kayseri, Kocasinan, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

GAZIU-FTR-FK-001

Identifier Type: -

Identifier Source: org_study_id