Effects of Corrective Exercises and Postural Education on Forward Head Posture

July 31, 2023 updated by: Yeditepe University

Effects of Corrective Exercises and Postural Education on Forward Head Posture- A Randomized Controlled Trial

Forward head posture is one of the most common postural problems that we face today. Sitting for long periods in poor posture and the excessive use of electronic devices has become a high risk for this postural abnormality.

The goal of this [interventional study] is to [provide the participants with simple and easy corrective exercises for this abnormal posture which they can do anywhere at any time and to provide postural education and awareness on the matter.

Study Overview

Detailed Description

Forward head posture is one of the most common postural problems that we face today. Sitting for long periods in poor posture and the excessive use of electronic devices has become a high risk for this postural abnormality.

The goal of this [interventional study] is to [provide the participants with simple and easy corrective exercises for this abnormal posture which they can do anywhere at any time and to provide postural education and awareness on the matter. Also, this study aims in comparing both the treatment and education.] in [the people who have forward head posture or are more likely to develop it]. The main question[s] it aims to answer are:

  • Does corrective exercises have any effect on improving forward head posture?
  • Does postural education has any effect on improving forward head posture?

Participants in [-Exercise group will perform corrective exercises for 6 weeks

  • Postural Education group will follow postural guidelines while doing daily tasks for 6 weeks
  • Control group will do nothing in 6 weeks]. Researchers will compare [Corrective Exercise group with Postural Education group and control group] to see if [corrective exercise group or postural education group has any effect on forward head posture and compare the results with the control group].

Study Type

Interventional

Enrollment (Actual)

46

Phase

  • Not Applicable

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

    • Atasehir
      • Istanbul, Atasehir, Turkey
        • Yeditepe 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

Description

Inclusion Criteria:

  1. Consent to participate in the study.
  2. Young & Middle-aged Adults between the ages of 20-40 years
  3. Craniovertebral angle less than or equal to 50°
  4. Shoulder Angle less than or equal to 52°

Exclusion Criteria:

  1. History of Trauma
  2. Acute Neck Injuries e.g., Whiplash
  3. Surgical history

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Corrective Exercises Group
The researcher will teach a total of 6 evidence-based corrective exercises and stretches. The participants will perform this for the prescribed time for a minimum of 3 and 5 times a week for a total of 6 weeks of the trial.
A total of 6 evidence-based exercises and stretches namely; Upper trapezius stretch, Sternocleidomastoid stretch, pectoral stretch; Chin tuck exercise, YTWL exercise, and resisted/isometric neck extension exercise will be prescribed to the exercise group while the postural education group will follow the guidelines provided by National Institutes of Health (NIH) for using computers and other sources. The control group will receive no intervention.
Active Comparator: Postural Education Group
Postural guidelines for doing daily activity especially sitting for prolonged periods and using electronic devices like computers and other electronic devices.
Postural guidelines for doing daily activity especially sitting for prolonged periods and using electronic devices like computers and other electronic devices.
No Intervention: Control Group
This group will not receive either of the above mentioned treatments.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Craniovertebral Angle
Time Frame: 6 weeks
The CVA is obtained by measuring the angle formed by the intersection of two lines drawn through particular anatomical landmarks and can be obtained using an image of the sagittal view of a person's head and neck. The first line is drawn from the tragus of the ear to the spinous process of the C7 vertebrae, and the second line is drawn through the spinous process of the C7 vertebrae horizontally. Although, there is no clear cut-off point threshold, identifying FHP for craniovertebral angle, in general, subjects with smaller craniovertebral angle i.e. less than 50 degrees have more Forward head posture
6 weeks
Shoulder Angle
Time Frame: 6 weeks
It is considered as the angle between a horizontal line through the spinous process of the C7 vertebra and a line passes from the midpoint of the shoulder joint through the spinous process of the seventh cervical vertebra.
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short Survey 36 Questionnaire
Time Frame: 6 weeks
The 36-Item Short Form Survey (SF-36) is an outcome measure instrument that is often used, a well-researched, self-reported measure of health. The SF-36 is often used as a measure of a person or population's quality of life (QOL).
6 weeks
Numeric Pain Rating Scale
Time Frame: 6 weeks
The Numeric Pain Rating Scale (NPRS) (an outcome measure) is a unidimensional measure of adult pain intensity. This 11-point numeric scale ranges from '0' representing one pain extreme (e.g., "no pain") to '10' representing the worst pain imaginable.
6 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Ebru Akbuga, Assistant Professor

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.

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)

May 12, 2023

Primary Completion (Actual)

June 30, 2023

Study Completion (Actual)

July 10, 2023

Study Registration Dates

First Submitted

May 11, 2023

First Submitted That Met QC Criteria

May 31, 2023

First Posted (Actual)

June 8, 2023

Study Record Updates

Last Update Posted (Actual)

August 1, 2023

Last Update Submitted That Met QC Criteria

July 31, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The participant data contains sensitive information like their contact and photographs. That is why this information will not be shared.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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