Investigation of Posture, Postural Stability and Core Endurance in Adults with Forward Head Posture: a Controlled Study

February 5, 2025 updated by: Gürkan Demirtas, Nigde Omer Halisdemir University
Forward head posture (FHP) is defined as the position in which the head is in front of the shoulder and is one of the most common musculoskeletal problems caused by increasing computer and smartphone use. The aim of this study is to compare the posture, postural stability and core endurance of participants with normal posture and participants with FHP.

Study Overview

Status

Completed

Conditions

Detailed Description

Forward head posture (FHP) is defined as the position in which the head is in front of the shoulder and is one of the most common musculoskeletal problems caused by increasing computer and smartphone use. FHP affects the muscle functions in the neck and thoracic region, reduces the expansion of the rib cage, diaphragm activation and strength with the kyphotic posture it causes, and causes a restrictive pulmonary disorder. In addition, FHP causes various postural alignment disorders in the body, leading to weakening of the core region and affecting postural stability. Posture analysis, postural stability and core endurance tests will be applied to the participants. The aim of this study is to compare the posture, postural stability and core endurance of participants with normal posture and participants with FHP.

Study Type

Observational

Enrollment (Actual)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Niğde, Turkey, 51200
        • Nigde Omer Halisdemir University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participants with a CVA of 50 degrees and less than 50 degrees will be included in the head forward posture group, and participants with a CVA above 50 degrees will be included in the control group.

Description

Inclusion Criteria:

-18-35 years

Exclusion Criteria:

  • Diagnosed respiratory, neurological, orthopaedic, psychiatric or cardiac problems
  • Pregnancy or breastfeeding
  • Having a history of neck trauma
  • Having undergone spinal surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Forward head posture group
-Craniovertebral angle <50
control
-Craniovertebral angle >50

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
postur
Time Frame: Baseline
A digital camera will be used to assess head and neck posture in the standing position.
Baseline
Postural stability
Time Frame: Baseline
Postural stability will be assessed in the bipedal position with eyes open and closed and in the unipedal position with eyes open. All tests will be measured using a force plate platform.
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Core endurance
Time Frame: Baseline
Core endurance is assessed using the trunk flexor test, trunk extensor test and side bridge test. All assessments are carried out during the time the individual is able to remain in bed.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Nigde Omer Halisdemir University

Investigators

  • Principal Investigator: Gürkan Demirtaş, Msc., Niğde Ömer Halisdemir Üniversitesi

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 8, 2024

Primary Completion (Actual)

January 8, 2025

Study Completion (Actual)

January 8, 2025

Study Registration Dates

First Submitted

November 29, 2024

First Submitted That Met QC Criteria

November 29, 2024

First Posted (Actual)

December 4, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 5, 2025

Last Verified

November 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2024/19-15

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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