RELATIONSHIP BETWEEN FORWARD HEAD POSTURE and HAMSTRING TIGHTNESS

December 6, 2024 updated by: Mark Refat Gabra Hana, Cairo University

RELATIONSHIP BETWEEN FORWARD HEAD POSTURE and HAMSTRING TIGHTNESS in YOUNG ADULTS

The purpose of this study will be to investigate:

  1. Relationship between forward head posture and hamstring tightness in young adults
  2. The gender specific effect (female versus male) on the relationship between forward head posture and hamstring tightness in young adults

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Detailed Description

Forward head posture imposes approximately 3.6 times more pressure on the neck than proper posture, and the prolonged burden of supporting the increased head weight can potentially cause neck pain, fatigue, and chronic musculoskeletal disorders. Hamstring tightness can cause posterior pelvic tilt, which leads to decreased lordosis of lumbar spine and resulting in LBP. Hamstring tightness can contribute to various issues, including muscle strains,loss of lumbar spine curvature, sacroiliac joint disorders, and plantar fasciitis. These problems primarily arise due to misalignment of the body and imbalanced force distribution between muscles and joints. Hamstring and sub-occipital muscles are connected by a neural system and sub-occipital muscles pass through the dura mater. this is called superficial back line (SBL), which connects the lower extremities, trunk, neck, and head protects the body's entire posterior surface and provides an important function of up-righting the body. There is still lack of research work about the relationship between FHP and hamstring muscle tightness and the gender-specific effect (female versus male) on the relationship between FHP and hamstring tightness in young adults.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
100

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

  • Egypt
      • Giza, Egypt
        • Faculty of Physical Therapy, Cairo 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

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

young adults with forward head posture

Description

Inclusion Criteria:

  • Both genders were included, with an age ranged between 18 and 25 years old.
  • Participants with a CVA equal to or less than 49° were included (Haytham M. Elhafez, 2023).
  • Body mass index was between 18 and 25 kg. /m2 (Haytham M. Elhafez, 2023).

Exclusion Criteria:

  • Systemic disease
  • History of hamstring injury within the last 2 years
  • Previous knee injury
  • Fracture in the spine or lower limb
  • Spinal or lower limb surgery
  • Pregnancy
  • Congenital deformity
  • Leg length discrepancy more than 2cm
  • Acute spasm of hamstring muscles
  • Neuromuscular disorders of the lower extremity, like stroke, muscular dystrophy and peripheral neuropathy
  • History of any malignancy or infectious disease
  • Spinal or limb deformities

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

Group / Cohort

A group or subgroup of participants in an observational study that is assessed for biomedical or health outcomes.
50 males
50 males with FHP and their BMI was between 20 and 25 kg/m2 ang ranged between 18 and 25 years
50 females
females with forward head posture and their BMI was between 20 and 25 kg/m2 and their age ranged between 18 and 25 years

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
craniovertebral angle and hamstring flexibility angle
Time Frame: july -november 2024
craniovertebral angle is the angle formed between a horizontal line through the spinous process of C7 and a line from the tragus of the ear craniovertebral angle was measured by Photogrammetry and kinovia software hamstring flexibility angle was measured by active knee extension test and kinovia software video analysis
july -november 2024

Collaborators and Investigators

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

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Cairo University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

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)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
July 29, 2024

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
October 29, 2024

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
November 29, 2024

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
December 6, 2024

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
December 6, 2024

First Posted (Estimated)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
December 10, 2024

Study Record Updates

Last Update Posted (Estimated)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
December 10, 2024

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
December 6, 2024

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
December 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • FHP and hamstring tightness

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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