NCT07019376

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 1, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

June 4, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 13, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 29, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2025

Completed
Last Updated

December 18, 2025

Status Verified

December 1, 2025

Enrollment Period

6 months

First QC Date

June 1, 2025

Last Update Submit

December 17, 2025

Conditions

Keywords

proprioceptionbiofeedbacklumbopelvicexercisepelvic swaybalanceendurance

Outcome Measures

Primary Outcomes (1)

  • Proprioception

    Proprioception of the lumbopelvic region is evaluated. The movement closest to the target point indicates good proprioception.

    one week

Secondary Outcomes (5)

  • Pelvic Sway

    one week

  • Balance

    one week

  • Core Muscle Endurance

    one week

  • Core Muscle Endurance

    one week

  • Core Muscle Endurance

    one week

Study Arms (3)

Visual biofeedback supported group

ACTIVE COMPARATOR

participants will perform lumbopelvic exercises for 8 weeks, 2 sessions per week for 8 weeks by providing visual biofeedback with a laser.

Other: Visual biofeedback supported lumbopelvic movement training

Visual biofeedback unsupported group

ACTIVE COMPARATOR

Participants will perform lumbopelvic exercises for 8 weeks, 2 sessions per week, without any biofeedback support.

Other: visual biofeedback unsupported lumbopelvic movement training

Control Group

NO INTERVENTION

control group not receiving any exercise

Interventions

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.

Visual biofeedback unsupported group

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 supported group

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nuh Naci Yazgan University

Kayseri, Kocasinan, 38170, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Fırat Kara, Phd Student

    Nuh Naci Yazgan University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
DIAGNOSTIC
Intervention Model
FACTORIAL
Model Details: Total of 3 groups including the control group who did not receive any training
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 1, 2025

First Posted

June 13, 2025

Study Start

June 4, 2025

Primary Completion

November 29, 2025

Study Completion

November 30, 2025

Last Updated

December 18, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations