Comparison of Deep Neck Flexor Strengthening and Motor Learning-Based Neuroplasticity Training for Forward Head Posture

January 1, 2026 updated by: Riphah International University

The aim of this randomized clinical trial is to compare the effects of deep neck flexor strengthening and motor learning-based neuroplasticity training on craniovertebral angle, deep neck flexor strength, proprioception, and symptom recurrence in individuals with forward head posture (FHP).

The study will be conducted at Riphah International University, Gulberg Green Campus. A total of 74 participants with forward head posture will be recruited using non-probability convenience sampling and randomly allocated into two groups (37 participants per group). Group A will receive deep neck flexor strengthening exercises, while Group B will receive motor learning-based neuroplasticity training. Both groups will undergo three sessions per week for four weeks. Assessments will be performed at baseline, post-intervention, and at one-month follow-up to assess symptom recurrence. Data will be analyzed using SPSS version 27.

Study Overview

Detailed Description

Forward head posture is a prevalent postural abnormality characterized by anterior translation of the head relative to the cervical spine. It is commonly observed among university students and young adults due to prolonged smartphone use, computer work, and sedentary lifestyles. Persistent FHP leads to muscular imbalance, weakness of the deep neck flexors, altered proprioception, and impaired neuromuscular control, often resulting in neck pain and functional limitations.

Deep neck flexor strengthening targets the longus colli and longus capitis muscles to restore cervical alignment and improve segmental stability. These exercises aim to correct muscular imbalances by enhancing endurance and motor control of the cervical stabilizers.

Motor learning-based neuroplasticity training is an emerging rehabilitation approach that emphasizes sensorimotor integration, task-specific training, and multisensory feedback. This approach facilitates cortical reorganization and re-establishment of disrupted cortico-spinal and cortico-subcortical pathways through repetitive, goal-oriented motor tasks. By integrating visual, auditory, and proprioceptive feedback, neuroplasticity-based training enhances postural awareness, motor planning, and long-term postural correction.

Despite evidence supporting both interventions individually, limited research has directly compared their effectiveness across postural, neuromuscular, and proprioceptive outcomes, particularly with respect to symptom recurrence. This study seeks to address this gap.

Previous studies have demonstrated that deep neck flexor strengthening significantly improves craniovertebral angle, reduces neck pain, and enhances cervical stability in individuals with forward head posture. Cervical stabilization programs have also shown positive effects on proprioception and neck repositioning accuracy.

Recent randomized controlled trials investigating motor learning-based neuroplasticity approaches have reported improvements in postural control, proprioception, and functional movement patterns through experience-dependent cortical plasticity. However, systematic reviews highlight inconsistent evidence regarding the superiority of strengthening exercises over motor learning-based interventions, with limited comparative trials and short-term follow-up.

Furthermore, evidence related to symptom recurrence and long-term sustainability of postural correction remains scarce. Therefore, a direct comparison of these two interventions is warranted.

Study Type

Interventional

Enrollment (Estimated)

74

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Capital
      • Islamabad, Capital, Pakistan, 44120
        • Riphah Postgraduate Lab, Riphah INternational University
        • Contact:
        • Principal Investigator:
          • Nimra Shahid, MSPT-OMPT*

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • University students aged 19-25 years
  • Both genders
  • Forward head posture with craniovertebral angle < 50°

Exclusion Criteria:

  • History of cervical spine injury or surgery
  • Chronic neck pain or recent therapy within six months.
  • Diagnosed with neurological, musculoskeletal, or visual disorders affecting posture.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental interventional group A (Deep neck flexor strengthening)
  • Chin tuck exercises
  • Isometric cervical flexion using gentle resistance
  • Prone head lift exercises
Chin tuck exercises, Isometric cervical flexion using gentle resistance, Prone head lift exercises. Frequency: 3 sessions per week, Duration: 4 weeks (12 sessions total).
Experimental: Experimental :interventional group B ( Motor learning based neuroplasticity training)
Task specific postural training using proprioceptive feedback, progressive balance and coordination and static and dynamic postural control tasks under different environmental conditions.
Task-specific postural training using visual (laser), auditory (metronome), and proprioceptive feedback. Progressive balance and coordination exercises under varying environmental conditions. Static and dynamic postural control tasks with intertrial variability. Frequency: 3 sessions per week, Duration: 4 weeks (12 sessions total)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Craniovertebral Angle (CVA)
Time Frame: Baseline to 4 weeks
Measured using digital photogrammetry and analyzed with software (e.g., Kinovea) to quantify forward head posture severity.
Baseline to 4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Deep Neck Flexor Strength
Time Frame: Baseline to 4 weeks
Assessed using the Deep Neck Flexor Endurance Test. It is performed in the supine line position with the chin hold and head off the couch and ask the patient to hold the position. The time of the hold will be recorded.
Baseline to 4 weeks
Cervical Proprioception
Time Frame: Baseline to 4 weeks
Measured using the Cervical Joint Repositioning Error Test with laser-guided repositioning.
Baseline to 4 weeks
Deep Neck Extensor Strength
Time Frame: Baseline to 4 weeks
Assessed using the Deep Neck Extensor Endurance Test. It is performed in the prone line position with the chin hold and head off the couch and ask the patient to hold the position. The time of the hold will be recorded.
Baseline to 4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Aisha Razzaq, PHD*, Riphah International University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 2, 2026

Primary Completion (Estimated)

December 30, 2026

Study Completion (Estimated)

January 20, 2027

Study Registration Dates

First Submitted

January 1, 2026

First Submitted That Met QC Criteria

January 1, 2026

First Posted (Actual)

January 13, 2026

Study Record Updates

Last Update Posted (Actual)

January 13, 2026

Last Update Submitted That Met QC Criteria

January 1, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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