Effects of Progressive Neck Motor Control Exercises With and Without Conventional Therapy in Text Neck Syndrome.(PNMCE-TNS)
Yes
1 other identifier
interventional
44
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
October 17, 2026
CompletedStudy Start
First participant enrolled
October 20, 2026
CompletedFirst Posted
Study publicly available on registry
October 23, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
October 23, 2026
October 1, 2026
2 months
October 17, 2026
October 17, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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
ACTIVE COMPARATORParticipants 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.
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.
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.
Eligibility Criteria
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
Related Links
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- 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.