Effects of Global Postural Reeducation on Forward Head Posture

Sponsor
Horus University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04723511
Collaborator
Cairo University (Other)
36
1
2
28.7
1.3

Study Details

Study Description

Brief Summary

This study aims at investigating the effects of application of a twelve sessions of Global Postural Re-education Technique (GPR) on Craniovertebral angle (CVA), functional abilities, stability of sense of position, cognitive abilities and treatment satisfaction.

Condition or Disease Intervention/Treatment Phase
  • Other: Global Postural Re-education
  • Other: Kendall exercises
N/A

Detailed Description

A sample of 36 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 2-3 sessions per week. The effect of these two treatments will be assessed by various variables including: forward head angle via photogrammetry and Kinovea App, functional abilities via neck disability index, stability of sense of position by Cervical Range of Motion instrument (CROM) ,cognitive abilities via Stroop and Montreal Cognitive Assessment (MOCA) tests and agreeability of treatment techniques via treatment satisfaction scale.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
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.
Primary Purpose:
Treatment
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
Actual Study Start Date :
Mar 9, 2021
Anticipated Primary Completion Date :
Dec 30, 2022
Anticipated Study Completion Date :
Jul 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: GPR

participants in this group receive global postural reeducation technique+ Kendall exercises

Other: Global Postural Re-education
treatment techniques include corrective exercises both local and global to correct forward head posture. first session will be to educate participants the treatment sequence. This will be a session of Kendall exercises as described below. This will followed be 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. Staring 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 a forth position of sitting on the floor position is introduced and performed for another 15 minutes. total of a session will then take a bout 90 minutes.

Active Comparator: Kendall

Kendall exercises

Other: Kendall exercises
exercises that correct upper crossed syndrome: Treatment sequence will be: a) Strengthen deep Cervical Flexors via Chin tucks. Repetition will be 15 times repeated for 3 sets. (b) Stretching the cervical extensors. This is held for 1 minute and repeated 5 times. (c) Strengthening shoulder retraction. Repetition will be 15 times repeated for 3 sets. (d) Stretching the pectoralis muscle. This is held for 1 minute and repeated 5 times.

Outcome Measures

Primary Outcome Measures

  1. craniovertebral angle [12 sessions with a rate of 2-3 sessions/week taking a 4-6 weeks /patient (according to patient's timetable)]

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

Secondary Outcome Measures

  1. Neck disability index [12 sessions with a rate of 2-3 sessions/week taking a 4-6 weeks /patient (according to patient's timetable)]

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

  2. Proprioceptive stability test [12 sessions with a rate of 2-3 sessions/week taking a 4-6 weeks /patient (according to patient's timetable)]

    By utilizing CROM testing the patients' sense of location precision

  3. Stroop test [12 sessions with a rate of 2-3 sessions/week taking a 4-6 weeks /patient (according to patient's timetable)]

    a word- color test to measure cognitive abilities of patients

  4. MOCA test [12 sessions with a rate of 2-3 sessions/week taking a 4-6 weeks /patient (according to patient's timetable)]

    a series of questions that enable to measure cognitive abilities of patients

  5. Treatment satisfaction scale [12 sessions with a rate of 2-3 sessions/week taking a 4-6 weeks /patient (according to patient's timetable)]

    a scale measuring the satisfaction and agreeability of the treatment according to patients' perspective

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients suffering from forward head Posture (CVA 50-40 degrees)

  • All subjects are medically stable and do not suffer from any other diseases which might affect the trial results.

  • 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.

  • Patient undergone other physical therapy program in the last three months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Horus University Damietta Egypt 34518

Sponsors and Collaborators

  • Horus University
  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Walaa Abu-Taleb, Principal investigator, Horus University
ClinicalTrials.gov Identifier:
NCT04723511
Other Study ID Numbers:
  • P.T.REC/012/002671
First Posted:
Jan 25, 2021
Last Update Posted:
Aug 15, 2022
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Walaa Abu-Taleb, Principal investigator, Horus University

Study Results

No Results Posted as of Aug 15, 2022