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Forward Head PostureNCT06850077

Comparison of Prefrontal Hemodynamic Responses and Balance Control Differences Based on Head Posture and Task Difficulty in Cognitive-Balance Tasks

An observational study of Forward Head Posture and Normal Head Posture, run by Sahmyook University at 1 site in South Korea.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 20 to 39 yearsHealthy volunteers can take part
Conditions the study is for
Forward Head Posture, Normal Head Posture
What is being tested?
Cognitive-Balance dual task
How many people
38 participants
Where
1 siteSouth Korea
Study dates
27 Apr 2025to 20 Oct 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 39 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Participants will be recruited from Samyook University(Seoul, South Korea) or local communities in Daegu or Seoul, South Korea. Recruitment will primarily target individuals who regularly engage in academic or sedentary activities. The study population will consist of individuals classified based on postural characteristics, specifically Forward Head Posture (FHP) or Normal Head Posture (NHP), assessed using craniovertebral angle (CVA) measurements. Recruitment will take place through campus advertisements, online postings, and word-of-mouth referrals.

Who may be able to join

  • 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

Who cannot join

  • Individuals with a history of spinal or musculoskeletal trauma or surgery
  • Individuals who have reported recent neck or shoulder pain

Trial locations and contacts

1 site in 1 country.

South Korea1 site
  • Sahmyook university

    Seoul, 노원구, 01759

Other trials in South Korea

About this study

  • 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.
Read the 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.

Being tested
Cognitive-Balance dual task
Keywords
forward head posture, dual task, prefrontal cortex, cognition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cognitive-Balance dual taskBehavioural

    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.

Study groups in NCT06850077
Study groupRoleWhat they receive
Forward head posture groupThe 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.
Receives: Behavioral: Cognitive-Balance dual task
Normal head posture groupThe 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.
Receives: Behavioral: Cognitive-Balance dual task

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The degree of hemodynamic response in the prefrontal cortex (PFC)

    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.

    Measured: From enrollment to 2 days

Secondary outcomes (1)
  1. Balance performance

    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.

    Measured: From enrollment to 2 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Feb 2025
  2. Study start27 Apr 2025
  3. Primary completion20 Oct 2025
  4. Study completion20 Oct 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
38 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06850077
Sponsor's protocol ID
SYU 2025-01-017-003
Status last verified
Sep 2025
First submitted
18 Feb 2025
Last updated
7 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: all collected IPD

Questions about this trial

What is this clinical trial studying?

An observational study of Forward Head Posture and Normal Head Posture, run by Sahmyook University at 1 site in South Korea.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The degree of hemodynamic response in the prefrontal cortex (PFC) (time frame: From enrollment to 2 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jan 2026.

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