- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04723511
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
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Damietta, Egypt, 34518
- Horus University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: GPR
participants in this group receive global postural reeducation technique+ Kendall exercises
|
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. |
|
Active Comparator: Kendall
Kendall exercises
|
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. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
craniovertebral angle
Time Frame: before and after 12 sessions
|
the angle formed between a horizontal line and a line extending from ear meatus and C7
|
before and after 12 sessions
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gaze Angle
Time Frame: before and after 12 sessions
|
the angle formed between the line extending from the tragus of the ear to the canthus of the eye.
|
before and after 12 sessions
|
|
Shoulder Angle
Time Frame: before and after 12 sessions
|
the angle formed between the line extending from C7 to acromion with horizontal line
|
before and after 12 sessions
|
|
Proprioceptive stability test
Time Frame: before and after 12 sessions
|
By utilizing CROM testing the patients' sense of location precision
|
before and after 12 sessions
|
|
Spinal mobility
Time Frame: before and after 12 sessions
|
Fingers to floor test using a tape measurement
|
before and after 12 sessions
|
|
Chest expansion
Time Frame: before and after 12 sessions
|
Axillary and Xyphoid chest expansion by the tape measurement
|
before and after 12 sessions
|
|
Cervical muscle strength and endurance
Time Frame: before and after 12 sessions
|
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.
|
before and after 12 sessions
|
|
Neck disability index
Time Frame: before and after 12 sessions
|
a scale that tests the effect of treatment on functional abilities of patients.
|
before and after 12 sessions
|
|
Pain intensity
Time Frame: before and after 12 sessions
|
Visual analogue scale is given to participants to select their pain scale level.
|
before and after 12 sessions
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Walaa Abu-Taleb, MSc, Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P.T.REC/012/002671
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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