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Forward Head PostureNCT04723511

Effects of Global Postural Reeducation on Forward Head Posture

A study testing Global Postural Re-education and Kendall exercises in people with Forward Head Posture, run by Horus University at 1 site in Egypt.

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

This study aims at investigating the effects of application of twelve sessions of Global Postural Re-education Technique (GPR) and Kendall Exercises (KE) on Craniovertebral angle (CVA), Gaze Angle (GA), Shoulders Angle (SA), Pain, functional abilities, Range of Motion, stability of sense of position, cervical muscle… Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Forward Head Posture
What is being tested?
Global Postural Re-education and Kendall exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
43 participants
Where
1 siteEgypt
Study dates
6 Feb 2021to 14 Oct 2021
Phase
Interventional
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 18 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Patients suffering from forward head Posture (CVA less than 50 degrees)
  • All subjects are medically stable and do not suffer from any other diseases which might affect the trial results.
  • BMI (18-24)
  • Patients willing and able to participate in this treatment program.
  • At least a moderate user of English.

Who cannot join

  • History of whiplash injury.
  • Patients who have undergone spinal surgeries or spinal fixations.
  • Patients with a neurologic deficit in their upper limbs, such as hypertonia, hypotonia, hyporeflexia, absence of reflex, and vertebral instability.
  • The patient underwent other physical therapy programs in the last three months.
  • Excessive use of smart technology

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Horus University

    Damietta, 34518

Other trials in Egypt

About this study

Official title: Effect of Global Postural Reeducation on Functional Abilities, Stability of Sense of Position, Cognitive Abilities and Treatment Satisfaction in Patients With Forward Head Posture

This study aims at investigating the effects of application of twelve sessions of Global Postural Re-education Technique (GPR) and Kendall Exercises (KE) on Craniovertebral angle (CVA), Gaze Angle (GA), Shoulders Angle (SA), Pain, functional abilities, Range of Motion, stability of sense of position, cervical muscle strength and endurance, Spinal mobility, and Chest Expansion.

Read the detailed description

A sample of 43 participants with a CVA less than 50 degrees will be randomly assigned to one of the two groups either receiving global postural reeducation added to traditional Kendall exercises or a group that receives Kendall Exercises only. Treatment sessions will be continued for a total of 12 sessions with a rate of 3 sessions per week. The effect of these two treatments will be assessed by various variables including: forward head angle, Gaze Angle and Shoulder angle via photogrammetry and Kinovea App, Pain intensity (VAS), functional abilities via neck disability index (NDI), cervical Range of motion and sense of position stability by Cervical Range of Motion instrument (CROM), Spinal mobility and chest expansion by tape measurement.

Being tested
Global Postural Re-education, Kendall exercises
Keywords
Forward Head Posture, Global Postural Re-education, Kendall Exercises, Rounded Shoulders, Postural Correction, Myofascial chains

What participants receive

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

  • Global Postural Re-educationOther

    treatment techniques include corrective exercises both local and global to correct forward head posture.

    first session will be to educate participants on the treatment sequence. This will be a session of Kendall's exercises as described below. This will followed be by performing GPR techniques of Anterior Chain stretch in the supine frog-like position for 20 minutes followed by posterior chain stretch against the wall for another 20 minutes. This is repeated in the first 6 sessions. Starting from the seventh session the time of holding each position is decreased to 15 minutes and a third position (standing against the wall) is introduced and performed for 15 minutes. Starting from the eighth session fourth position of sitting on the floor position is introduced and performed for another 15 minutes. total of a session will then take about 90 minutes.

    Pre-treatment diaphragmatic release and deep breathing exercises are applied at the beginning of each session

  • Kendall exercisesOther

    exercises that correct upper crossed syndrome:

    The treatment sequence will be:

    1. Strengthen deep Cervical Flexors via Chin tucks. Repetition will be repeated 10 times for 5 sets. (b) Stretching the cervical extensors. This is held for 1 minute and repeated 5 times. (c) Strengthening shoulder retraction. Repetition will be repeated 10 times for 5 sets. (d) Stretching the pectoralis muscle. This is held for 1 minute and repeated 5 times.

    Exercises will be progressed as the sessions develop.

Study groups in NCT04723511
Study groupRoleWhat they receive
GPRExperimentalparticipants in this group receive global postural reeducation technique+ Kendall exercises
Receives: Other: Global Postural Re-education; Other: Kendall exercises
KendallActive comparatorKendall exercises
Receives: Other: Kendall exercises

What is being measured

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

  1. craniovertebral angle

    the angle formed between a horizontal line and a line extending from ear meatus and C7

    Measured: before and after 12 sessions

Secondary outcomes (8)
  1. Gaze Angle

    the angle formed between the line extending from the tragus of the ear to the canthus of the eye.

    Measured: before and after 12 sessions

  2. Shoulder Angle

    the angle formed between the line extending from C7 to acromion with horizontal line

    Measured: before and after 12 sessions

  3. Proprioceptive stability test

    By utilizing CROM testing the patients' sense of location precision

    Measured: before and after 12 sessions

  4. Spinal mobility

    Fingers to floor test using a tape measurement

    Measured: before and after 12 sessions

  5. Chest expansion

    Axillary and Xyphoid chest expansion by the tape measurement

    Measured: before and after 12 sessions

  6. Cervical muscle strength and endurance

    Biofeedback stabiliser is used to measure the maximum time the muscles could hold in addition to time the contraction of 50% maximum muscle contractionis maintained.

    Measured: before and after 12 sessions

  7. Neck disability index

    a scale that tests the effect of treatment on functional abilities of patients.

    Measured: before and after 12 sessions

  8. Pain intensity

    Visual analogue scale is given to participants to select their pain scale level.

    Measured: before and after 12 sessions

Timeline

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

  1. First posted25 Jan 2021
  2. Study start6 Feb 2021
  3. Primary completion4 Oct 2021
  4. Study completion14 Oct 2021

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
43 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04723511
Sponsor's protocol ID
P.T.REC/012/002671
Status last verified
Aug 2024
First submitted
15 Jan 2021
Last updated
7 Aug 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: These data are case sensitive and considered confidential regarding my supervisors' opinion and participants' request , So, upon their request I prefer to not share individual participant data (IPD) with other researchers

Publications

  • Abu-Taleb W, Yamany AA, Aneis YM, Abu El Kasem ST. Effect of adding global postural reeducation to kendall exercises for treating asymptomatic forward head posture: A single-blinded randomized controlled trial. J Bodyw Mov Ther. 2025 Jun;42:938-947. doi: 10.1016/j.jbmt.2025.01.039. Epub 2025 Feb 6.

    PubMed 40325777

Questions about this trial

What is this clinical trial studying?

A study testing Global Postural Re-education and Kendall exercises in people with Forward Head Posture, run by Horus University at 1 site in Egypt.

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 5 inclusion and 5 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 Aug 2024. 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 Egypt. 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?

craniovertebral angle (time frame: before and after 12 sessions). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04723511, which also lists 1 linked publication.

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 Aug 2024.

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