NCT06972316

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 9, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

May 1, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

May 15, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 10, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2025

Completed
Last Updated

April 9, 2026

Status Verified

May 1, 2025

Enrollment Period

7 months

First QC Date

May 1, 2025

Last Update Submit

April 6, 2026

Conditions

Keywords

Text Neck Syndromepostural reeducation

Outcome Measures

Primary Outcomes (1)

  • pain intensity level

    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.

    Baseline (pre-intervention) and at 4 weeks (post-intervention)

Secondary Outcomes (1)

  • Craniovertebral angle and shoulder angle

    Baseline (pre-intervention) and at 4 weeks (post-intervention)

Study Arms (2)

Control group

EXPERIMENTAL

Control group (A) INCLUDED 30 arm All participants received conventional treatment consisting of stretching and strengthening exercises, including pectoral stretching, upper trapezius stretching, levator scapulae stretching, chin tucks, shoulder shrugs, and scapular retraction. Exercises were performed actively under therapist supervision, which included observation, correction of faulty performance, and timing of stretching exercises with a stopwatch.

Other: The Global postural reeducation

Experimental Group B Global Postural Reeducation

EXPERIMENTAL

Control group (B) INCLUDED 30 arms with text neck syndrome; they will received GPR in addition to conventional treatment, In addition to conventional treatment, participants received GPR according to the protocol described by Souchard.

Other: Traditional treatments

Interventions

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

Control group

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

Experimental Group B Global Postural Reeducation

Eligibility Criteria

Age18 Years - 44 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dokki

Cairo, Egypt

Location

Study Officials

  • Heba Heba Saeid Mohamed Ahmed, master

    Assist. lecture faculty of physical therapy Cairo university

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
Randomization was performed using computer-generated numbers placed in opaque sealed envelopes. Participants were assigned to one of two groups in a 1:1 ratio. Allocation was conducted by an author not involved in data collection or treatment. To maintain allocation concealment, envelopes were opened only at the time of participant enrollment. Participants were blinded to their group allocation until study completion.²0 All participants provided written informed consent.
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
assistant lecturer of physical therapy for basic science department Cairo University

Study Record Dates

First Submitted

May 1, 2025

First Posted

May 15, 2025

Study Start

February 9, 2025

Primary Completion

September 10, 2025

Study Completion

November 30, 2025

Last Updated

April 9, 2026

Record last verified: 2025-05

Locations