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NCT Number: NCT07681687

Sensory Motor Control and Muscle Energy Technique for Chronic Mechanical Neck

A randomized controlled trial to evaluate the effectiveness of Sensory Motor Control training combined with Muscle Energy Technique in reducing pain and improving function, cervical range of motion, proprioception, and kinesiophobia in individuals with chronic mechanical neck pain

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Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Max Spine Rehab Center, Max Health Hospital

Islamabad, Pakistan

Location status: Recruiting

Location contact

Dr. Abdul Ghafoor Sajjad, BSPT, PP-DPT, MS-OMPT

CONTACT

[email protected]

00923335468034

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Adults aged 18- 35years,Clinical diagnosis of cervical pain due to strain, degenerative changes of the spine, e.g., spondylosis.Willingness to participate and provide written informed consent,Presence of reduced cervical range of motion, especially in the upper cervical spine,Symptom duration in chronic patients is more than 3 months.

Exclusion criteria

History of surgery to the cervical spine in the last 6 months,Neurological deficits or signs of cervical myelopathy,Presence of systemic conditions (e.g., rheumatoid arthritis, cancer, infections) affecting the spine,Pregnancy or known vestibular disorders,Inability to comply with study procedures or follow-up schedule

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Treatment and study plan

Muscle energy technique for MET only group

Other

Participants will receive Post-Isometric Relaxation (PIR) techniques targeting the upper trapezius, levator scapulae, sternocleidomastoid, deep neck flexors, deep neck extensors, and scalene muscles. Each technique involves a gentle isometric contraction (5-10 seconds) followed by relaxation and stretching to a new barrier, repeated 3-5 times. Both groups will receive hot pack therapy (10 minutes), manual therapy (5 minutes), and MET. The intervention group will additionally receive Sensory Motor Control (SMC) training. Participants will undergo a structured SMC program including oculomotor exercises, head-eye coordination training, figure-of-eight tracking, gaze stability, and gaze-shifting exercises. The program is designed to improve cervical proprioception, postural control, movement accuracy, and range of motion while reducing pain and functional disability in individuals with chronic mechanical neck pain. Sessions will be supervised and progressed according to patient tolerance.

MET +SMC for experimental group

Other

articipants in the experimental group will receive a combination of Muscle Energy Technique (MET) and Sensory Motor Control (SMC) Training. Treatment sessions will be conducted under the supervision of a physiotherapist. MET will be applied to the shortened cervical muscles, including the upper trapezius and levator scapulae, using post-isometric relaxation techniques to reduce muscle tightness, improve cervical mobility, and decrease pain.

Following MET, participants will perform a structured SMC training program aimed at improving cervical proprioception, eye-head coordination, gaze stability, movement control, balance, and postural awareness. The SMC program will include the following exercises:

Smooth Horizontal and Vertical Tracking: A card measuring approximately 10-15 cm × 7-10 cm will be placed 2 meters from the participant. In Level 1, participants move their eyes while keeping the head stationary; in Level 2, they move the head while maintaining visual fixation on the targe

Primary outcomes

  1. NPRS

    Time frame: From enrollment to pretreatment assesment and than after 6 weeks post treatment assesment measured by NPRS

    The Numeric Pain Rating Scale (NPRS) will be used to assess the intensity of neck pain experienced by participants. The NPRS is a valid, reliable, and widely used self-reported measure of pain intensity. Participants will be asked to rate their current neck pain on an 11-point scale ranging from 0 to 10, where 0 indicates "no pain" and 10 indicates "the worst pain imaginable."

    Participants will select the number that best represents their average pain intensity over the preceding 24 hours. NPRS scores will be recorded at baseline and after completion of the intervention period. A reduction in NPRS score will indicate improvement in pain symptoms. The scale has demonstrated excellent reliability and responsiveness in individuals with musculoskeletal disorders, including chronic mechanical neck pain.

    Scoring:

    0 = No pain 1-3 = Mild pain 4-6 = Moderate pain 7-10 = Severe pain

    Interpretation:

    Lower scores indicate lower pain intensity, while higher scores indicate greater pain intensi

Secondary outcomes

  1. NDI

    Time frame: 6 WEEKS

    The Neck Disability Index (NDI) will be used to assess self-reported disability and functional limitations associated with chronic mechanical neck pain. The NDI is one of the most widely used, valid, and reliable questionnaires for evaluating neck-related disability in both clinical practice and research.

    The questionnaire consists of 10 items that assess the impact of neck pain on daily activities, including pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation. Each item is scored on a 6-point scale (0-5), with higher scores indicating greater disability. The total score ranges from 0 to 50 points and can also be expressed as a percentage by multiplying the total score by two.

    Participants will complete the NDI at baseline and after the intervention period. Changes in NDI scores will be used to determine the effectiveness of the treatment in improving functional status and reducing disability related to neck pain.

    Scori

  2. Joint Position Error (JPE)

    Time frame: 6 WEEKS

    Cervical Joint Position Error (JPE) testing will be used to assess cervical proprioception and sensorimotor control in participants with chronic mechanical neck pain. The test evaluates the individual's ability to accurately reposition the head to a neutral starting position after active cervical movement, reflecting the integrity of cervical joint position sense.

    Participants will be seated comfortably with a laser pointer attached to a headband, facing a target placed approximately 90 cm away at eye level. The participant will first establish a neutral head position, which will be marked on the target. With eyes closed, the participant will actively move the head into flexion, extension, right rotation, and left rotation, and then attempt to return to the original neutral position.

    The distance between the original target point and the repositioned point will be measured and converted into degrees of error, representing the joi

  3. INCLINOMETER

    Time frame: 6WEEKS

    A digital inclinometer will be used to assess cervical range of motion (ROM) in participants with chronic mechanical neck pain. The inclinometer is a valid, reliable, and objective tool for measuring cervical spine movements and detecting changes following therapeutic interventions.

    Cervical ROM will be assessed in the following directions:

    Flexion Extension Right lateral flexion Left lateral flexion Right rotation Left rotation

    During assessment, participants will be seated comfortably in an upright position with their feet supported on the floor. The inclinometer will be positioned according to standardized measurement procedures, and participants will be instructed to move their head actively to the maximum pain-free range in each direction. Three measurements will be recorded for each movement, and the average value will be used for analysis.

    Assessments will be performed at baseline and after completion of the intervention period. ROM values will be recorded in degrees (°). A

  4. Tampa Scale

    Time frame: 6 weeks

    The Tampa Scale of Kinesiophobia is a self-reported questionnaire used to assess fear of movement and re-injury associated with pain. It measures the extent to which individuals believe that physical activity may cause further injury or increase pain. The scale consists of 17 items, each scored on a 4-point Likert scale ranging from 1 (strongly disagree) to 4 (strongly agree). Total scores range from 17 to 68, with higher scores indicating greater fear of movement and avoidance behaviors.

    In clinical trials involving chronic mechanical neck pain, the TSK is used to evaluate changes in pain-related fear and movement avoidance following therapeutic interventions. It is a reliable and valid tool for assessing psychological factors that may contribute to pain persistence, disability, and reduced participation in daily activities. A reduction in TSK scores after treatment indicates improved confidence in movement and decreased fear of pain-related activities

Study contacts

Contact information is provided by the study sponsor or research team.

MUHAMMAD ASHAR RAFI, DPT, MS-NMPT

CONTACT

[email protected]

0092-308-3407837

Maryam Jawaid, DPT

CONTACT

[email protected]

+923199564534

Sponsors and collaborators

Lead sponsor

Ibadat International University, Islamabad

Other

Registry information

Official study title

Effectiveness of Sensory Motor Control and Muscle Energy Techniques on Chronic Mechanical Neck Pain

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 2, 2026
Registry last updated
Jul 2, 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.

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