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Effects of Global Postural Reeducation on Forward Head Posture

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04723511
Enrollment
43
Registered
2021-01-25
Start date
2021-02-06
Completion date
2021-10-14
Last updated
2024-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Forward Head Posture

Keywords

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

Brief 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 strength and endurance, Spinal mobility, and Chest Expansion.

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.

Interventions

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

exercises that correct upper crossed syndrome: The treatment sequence will be: a) 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.

Sponsors

Cairo University
CollaboratorOTHER
Horus University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

The enrolled participants will be masked (single blind study) and randomly assigned into two groups without being informed whether they are in the control or the study(experimental) group.

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* 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.

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
craniovertebral anglebefore and after 12 sessionsthe angle formed between a horizontal line and a line extending from ear meatus and C7

Secondary

MeasureTime frameDescription
Shoulder Anglebefore and after 12 sessionsthe angle formed between the line extending from C7 to acromion with horizontal line
Proprioceptive stability testbefore and after 12 sessionsBy utilizing CROM testing the patients' sense of location precision
Spinal mobilitybefore and after 12 sessionsFingers to floor test using a tape measurement
Gaze Anglebefore and after 12 sessionsthe angle formed between the line extending from the tragus of the ear to the canthus of the eye.
Cervical muscle strength and endurancebefore and after 12 sessionsBiofeedback stabiliser is used to measure the maximum time the muscles could hold in addition to time the contraction of 50% maximum muscle contractionis maintained.
Neck disability indexbefore and after 12 sessionsa scale that tests the effect of treatment on functional abilities of patients.
Pain intensitybefore and after 12 sessionsVisual analogue scale is given to participants to select their pain scale level.
Chest expansionbefore and after 12 sessionsAxillary and Xyphoid chest expansion by the tape measurement

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026