Skip to main content
OpenTrials
Completed

NCT Number: NCT06972316

Global Postural Re-education in Text Neck Syndrome

The purpose of the study is to:

Investigate if there was effect of global postural re-education in individuals with text neck syndrome.

The Global postural reeducation (GPR) is a series of postures and gentle active movements are performed aimed at stretching shortened muscles, decompressing and aligning joints, with breath¬ing control, contractions of antagonist muscles and sen¬sory integration exercises to work on proprioceptive af¬ferents and re-educate postural control The study was testing the following null hypothesis There was no effect of Global postural in individuals with text neck syndrome.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–44 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dokki

Cairo, Egypt

About this study

This study was conducted in the research laboratory section, Faculty of Physical Therapy, Cairo University. The purpose of the current study was to investigate the effect of global postural reeducation on neck pain intensity, neck disability craniovertebral angle, shoulder angle, cervical range of motion, and cervical proprioception in individuals with text neck syndrome.

This study is a Pre- test post- test single blind randomized controlled trial. • Subjects' selection:

A. Participants:

  • 60 Participants from both genders diagnosed by physician as TNS
  • Their age ranging from 18-44 years old
  • Their body mass index ranging from (18-30) Kg/m2
  • Their using mobile phones for more than 3-4 hours per day was assessed by using The Arabic version of the smartphone addiction scale
  • Informed consent (Appendix I) attained from each participant after clarifying the scope and purpose of the research and ensuring them of their right to decline at any time and of the privacy of any information obtained.

B- Sample size:

The sample size was calculated using the G*Power software (version 3.0.10). F-test MANOVA within and between interaction effects was selected. Considering a power of 0.80, an α level of 0.05 (2 tailed) and effect size of 0.37; two groups and number of measurements two, a generated sample size of at least 60 subjects,30 subjects per group was required.

C. Randomization:

Concealed allocation was performed by an independent person who not involved in either recruitment or treatment of the patients. He used individually, sequentially numbered index cards containing the randomly assigned intervention groups (A and B) that folded and placed in sealed, opaque envelopes. the researcher opened the envelope before the 1st session and proceeds with the treatment on the initial examination day according to the group assignment.

D. Groups:

Participants assigned at random into 2 equal groups. Control group (A) received conventional treatment only. Experimental group (B) received Global postural reeducation in addition to conventional treatment E. Incluction critrria

  • participants aged range from 18-44 years old .
  • participants Body mass index between (18-30) Kg/m2
  • participants using mobile phones for more than 3-4 hours per day assessed by using The Arabic version of the smartphone addiction scale (short version). F. Exclusion criteria

The subject excluded if they had the following:

(1) history of neck pathology; (2) musculoskeletal disease or anomaly; (3) history of spinal or neck surgery; (4) recent surgery; (5) chronic medical illness; or (6) receipt of any treatment for the neck in the preceding three months.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The subject included if they had the following:
  • diagnosed by physician as text neck syndrome
  • Using mobile phones for more than 3-4 hours per day
  • pain score more than 4 on the visual analog scale.

Exclusion criteria

  • The subject excluded if they had the following:
  • history of neck pathology; (2) musculoskeletal disease or anomaly; (3) history of spinal or neck surgery; (4) recent surgery; (5) chronic medical illness; or (6) receipt of any treatment for the neck in the preceding three months.

Treatment and study plan

The Global postural reeducation

Other

The Global postural reeducation (GPR) is a series of postures and gentle active movements are performed aimed at stretching shortened muscles, decompressing and aligning joints, with breath¬ing contro

traditional treatments

Other

Thermotherapy (hot packs) , Dynamic neck exercises, stretching exercise and posture advice

Primary outcomes

  1. pain intensity level

    Time frame: Baseline (pre-intervention) and at 4 weeks (post-intervention)

    assessed using the Visual Analog Scale (VAS), a 100-mm line ranging from "no pain" (0 mm) on the left to "worst pain" (100 mm) on the right. Scores were based on self-reported symptom measures.

Secondary outcomes

  1. Craniovertebral angle and shoulder angle

    Time frame: Baseline (pre-intervention) and at 4 weeks (post-intervention)

    Craniovertebral angle (CVA): Is the angle formed between a horizontal line through the spinous process of C7 and a line from the tragus of the ear (Ruivo et al., 2014). angles less than 49° were considered as FHP (Mani et al., 2017).

    Shoulder angle (SA): is the angle formed at a line between the center of the humerus and spinous process of C7 and the horizontal line through the center of the humerus. SA less than 52° were considered as RSP (Ruivo et al., 2014).

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Effect of Global Postural Re-education in Individuals With Text Neck Syndrome

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
May 15, 2025
Registry last updated
Apr 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.