- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06850077
Comparison of Prefrontal Hemodynamic Responses and Balance Control Differences Based on Head Posture and Task Difficulty in Cognitive-Balance Tasks
- Recent studies have shown that individuals with forward head posture (FHP) experience not only impaired balance control but also cognitive deficits.
- Using a balance-cognitive dual-task paradigm, this study aims to explore the relationship between balance ability and Prefrontal cortex(PFC) oxygenation levels(△HbO2) in individuals with FHP compared to those with normal head posture(NHP).
- By analyzing differences in frontal lobe activation based on task difficulty, this study is expected to provide practical data for designing balance training and cognitive-motor intervention programs tailored to individuals with FHP.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
- This study is a cross-sectional study aiming to investigate the differences in balance ability between individuals with forward head posture (FHP) and those with normal head posture (NHP), as well as the differences in frontal lobe oxygenation levels during a balance-cognitive dual task.
Study participants will be assigned to receive two groups: (a) Forward head posture (b) Normal head posture. Each group will perform three balance tasks while simultaneously completing three cognitive tasks. To determine the differences, the primary outcome will assess prefrontal cortex (PFC) hemodynamic response, and the secondary outcome will assess balance ability.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
노원구
-
Seoul, 노원구, South Korea, 01759
- Sahmyook University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy adults aged 20 to 39 years
- Classified as having Forward Head Posture (FHP) or Normal Head Posture (NHP) based on Craniovertebral Angle (CVA) measurement
Exclusion Criteria:
- Individuals with a history of spinal or musculoskeletal trauma or surgery
- Individuals who have reported recent neck or shoulder pain
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Forward head posture group
The experiment will be conducted for approximately 30 minutes. It will comprise cognitive tasks with three levels of difficulty and balance tasks, with task difficulty adjusted according to each participant's cognitive and balance abilities. During the experiment, changes in cerebral blood flow, cognitive performance, and balance ability will be assessed and analyzed. |
The cognitive-balance dual task consists of three levels of difficulty and is performed simultaneously. The cognitive tasks include the N-back test, while the balance tasks consist of static balance tasks. |
|
Normal head posture group
The experiment will be conducted for approximately 30 minutes. It will comprise cognitive tasks with three levels of difficulty and balance tasks, with task difficulty adjusted according to each participant's cognitive and balance abilities. During the experiment, changes in cerebral blood flow, cognitive performance, and balance ability will be assessed and analyzed. |
The cognitive-balance dual task consists of three levels of difficulty and is performed simultaneously. The cognitive tasks include the N-back test, while the balance tasks consist of static balance tasks. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The degree of hemodynamic response in the prefrontal cortex (PFC)
Time Frame: From enrollment to 2 days
|
Hemodynamic response changes in the prefrontal cortex (PFC) will be assessed by measuring variations in oxyhemoglobin (HbO) concentration using functional near-infrared spectroscopy (fNIRS).
The study will compare HbO concentration changes between the control and experimental groups during cognitive-balance task performance.
|
From enrollment to 2 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance performance
Time Frame: From enrollment to 2 days
|
Static and dynamic balance performance will be assessed using the Good Balance system (Metitur, Finland). The assessment will be conducted on a triangular platform by measuring changes in the center of pressure (COP), regardless of foot position. The results will be reported as variations in COP displacement and velocity. Dynamic balance performance will be assessed using the Four Square Step Test (FSST). Participants will step in four quadrants formed by rods or tape arranged in a cross pattern. The time taken to complete the FSST will be recorded in seconds. |
From enrollment to 2 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SYU 2025-01-017-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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