NCT07892131

Brief Summary

This study aims to compare the effects of Progressive Neck Motor Control Exercises (PNMCE) with and without conventional physiotherapy in patients with Text Neck Syndrome. It will evaluate the effectiveness of both treatment approaches in reducing neck pain, improving cervical range of motion, correcting posture, and enhancing functional ability. The study will determine which treatment approach provides better clinical outcomes.

Trial Health

63
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Trial Health Score

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

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Oct 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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 Progress6%
Oct 2026Dec 2026

First Submitted

Initial submission to the registry

October 17, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

October 20, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 23, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

October 23, 2026

Status Verified

October 1, 2026

Enrollment Period

2 months

First QC Date

October 17, 2026

Last Update Submit

October 17, 2026

Conditions

Keywords

Progressive Neck Motor Control ExercisesCraniovertebral AngleNeck Disability IndexForward Head PostureCervical Range of Motion

Outcome Measures

Primary Outcomes (5)

  • NUMERICAL PAIN RATING SCALE

    11-point numeric with 0 representing No pain, 1-3 representing Mild Pain (nagging, annoying, interfering little with ADLs), 4-6 representing Moderate Pains (interferes significantly with ADLs), 7-10 representing Sever Pain

    Baseline and post treatment after six weeks

  • UNIVERSAL GONIOMETER

    Cervical range of motion (ROM) will be assessed using a universal goniometer in sagittal, frontal, and transverse planes. Measurements will be taken in sitting with the thoracic spine stabilized, except rotation (supine), using anatomical landmarks (tragus, occiput, acromion, and C7). Three trials per direction will be averaged with 30-second rest intervals

    Baseline and post treatment after six weeks

  • CRANIOVERTEBRAL ANGLE (CVA) - PHOTOGRAPHIC ANALYSIS

    Head and neck posture will be assessed using standardised photographic methods consistent with those described in the reference study.(1) The tragus, pogonion, eye corner, and acromion process are anatomical features that will be delineated at C7. A digital camera will be placed three meters away from the subject at shoulder height, and image analysis software will be used to determine the CVA.

    Baseline and post treatment after six weeks

  • NECK DISABILITY INDEX (NDI)

    0-8% indicates no disability, 10-28% indicates mild disability, 30-48% indicates moderate impairment, 50-64% indicates severe disability, and ≥65% indicates complete disability. The total scores range from 0 to 50 and are converted to percentages.

    Baseline and post treatment after six weeks

  • ANEROID SPHYGMOMANOMETER

    To simplify and track craniocervical flexion exercises for deep cervical flexor muscle training, a modified aneroid sphygmomanometer is employed as a pressure biofeedback tool. The sphygmomanometer\'s inflatable bladder was placed under the cervical lordosis and inflated to a baseline pressure of 20 mmHg. There is evidence that the Craniocervical Flexion Test (CCFT) has excellent reliability and acceptable validity when using a modified aneroid sphygmomanometer.

    Baseline and post treatment after six weeks

Study Arms (2)

Progressive Neck Motor Control Exercises and Conventional Therapy

EXPERIMENTAL

Participants will receive conventional physiotherapy, including hot pack and TENS application (15 minutes), cervical joint mobilization (Maitland Grades I-III, 3 sets of 30 seconds per segment), and soft tissue mobilization/myofascial release of the upper trapezius, levator scapulae, and sternocleidomastoid (10 minutes). Postural correction and ergonomic education will be provided, followed by the full PNMCE program.

Other: Progressive Neck Motor Control Exercises and Conventional Therapy

Progressive Neck Motor Control Exercises

ACTIVE COMPARATOR

Participants will receive patient education on disease management, diet, activity modification, and posture, followed by a 6-week Progressive Neck Muscle Control Exercise (PNMCE) program. Weeks 1-2: Supine/prone chin tucks, craniocervical flexion (20-22 mmHg), and upper/lower limb exercises; Weeks 3-4: Quadrupedal/standing chin tucks, limb exercises, wall angels, and craniocervical flexion (24-26 mmHg). Weeks 5-6: Swiss ball exercises, resisted chin tucks, and upper limb strengthening with TheraBand (red to green to blue), progressing to 28-30 mmHg; all exercises performed for 2 sets of 10 repetitions, with resistance increased according to tolerance.

Other: Progressive Neck Motor Control Exercises

Interventions

Participants will receive patient education on disease management, diet, activity modification, and posture, followed by a 6-week Progressive Neck Muscle Control Exercise (PNMCE) program. Weeks 1-2: Supine/prone chin tucks, craniocervical flexion (20-22 mmHg), and upper/lower limb exercises; Weeks 3-4: Quadrupedal/standing chin tucks, limb exercises, wall angels, and craniocervical flexion (24-26 mmHg). Weeks 5-6: Swiss ball exercises, resisted chin tucks, and upper limb strengthening with TheraBand (red to green to blue), progressing to 28-30 mmHg; all exercises performed for 2 sets of 10 repetitions, with resistance increased according to tolerance.

Progressive Neck Motor Control Exercises

Participants will receive conventional physiotherapy, including hot pack and TENS application (15 minutes), cervical joint mobilization (Maitland Grades I-III, 3 sets of 30 seconds per segment), and soft tissue mobilization/myofascial release of the upper trapezius, levator scapulae, and sternocleidomastoid (10 minutes). Postural correction and ergonomic education will be provided, followed by the full PNMCE program.

Progressive Neck Motor Control Exercises and Conventional Therapy

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Individuals aged 18-40 years of both gender
  • Text Neck Syndrome confirmed by: daily smartphone/tablet use ≥ 4 hours
  • AND neck pain onset linked to device use for a minimum of 3 months.
  • Forward Head Posture confirmed by craniovertebral angle (CVA) \<50° on standardised photographic assessment.
  • Neck pain intensity ≥ 4 on the Numerical Pain Rating Scale (NPRS).

You may not qualify if:

  • Cognitive impairment limiting ability to follow instructions.
  • Use of cervical orthosis or splint devices.
  • Diagnosed systematic joint or muscle disease (e.g., fibromyalgia, rheumatoid arthritis).
  • Serious systemic diseases or neurological disorders (e.g., cervical radiculopathy, myelopathy,trigeminal neuralgia).
  • Pregnancy or breastfeeding.
  • History of surgery or significant trauma to the cervical region.
  • Positive vertebrobasilar artery test.
  • Confirmed cervical fracture or congenital cervical deformity.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Management & Technology

Lahore, Punjab Province, 54000, Pakistan

Location

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This study aims to compare the effects of Progressive Neck Motor Control Exercises (PNMCE) with and without conventional physiotherapy in patients with Text Neck Syndrome. It will evaluate the effectiveness of both treatment approaches in reducing neck pain, improving cervical range of motion, correcting posture, and enhancing functional ability. The study will determine which treatment approach provides better clinical outcomes.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

October 17, 2026

First Posted

October 23, 2026

Study Start

October 20, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

October 23, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
6 months after the publication of the manuscript.
Access Criteria
This data can be requested from the corresponding author.

Locations