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Sensory Motor Control and Muscle Energy Technique for Chronic Mechanical Neck

2026年6月26日 更新者:Ibadat International University, Islamabad

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

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

調査の概要

研究の種類

介入

入学 (推定)

52

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

      • Islamabad、パキスタン
        • 募集
        • Max Spine Rehab Center, Max Health Hospital
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

いいえ

説明

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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研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:診断
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
プラセボコンパレーター:MET only group

Participants allocated to Group A will receive Muscle Energy Technique (MET) using the Post-Isometric Relaxation (PIR) method targeting the cervical musculature. The intervention will be administered by a licensed physiotherapist and will include treatment of the upper trapezius, levator scapulae, sternocleidomastoid, deep neck flexors, deep neck extensors, and scalene muscles.

For each muscle, the therapist will position the muscle at its initial resistance barrier and instruct the participant to perform a gentle isometric contraction (approximately 20-30% of maximal effort) against therapist resistance for 5-10 seconds, followed by complete relaxation. The therapist will then move the muscle to the new barrier and maintain the stretch for 10-15 seconds. This sequence will be repeated 3-5 times for each muscle group.

The treatment protocol includes:

Upper Trapezius: Side-bending of the cervical spine away from the affected side following isometric contraction.

Levator Scapulae:

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.
実験的:MET + SMC group
Moist Hot Pack for 10 mins,TENS for 10 mins,Manual therapy for 5 mins,MET + SMC exercercises for neck

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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
NPRS
時間枠: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

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

二次結果の測定

結果測定
メジャーの説明
時間枠
NDI
時間枠: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

6 WEEKS
Joint Position Error (JPE)
時間枠: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

6 WEEKS
INCLINOMETER
時間枠: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

6WEEKS
Tampa Scale
時間枠: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

6 weeks

協力者と研究者

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年1月1日

一次修了 (推定)

2026年8月15日

研究の完了 (推定)

2026年9月1日

試験登録日

最初に提出

2026年6月26日

QC基準を満たした最初の提出物

2026年6月26日

最初の投稿 (実際)

2026年7月2日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月2日

QC基準を満たした最後の更新が送信されました

2026年6月26日

最終確認日

2026年1月1日

詳しくは

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米国FDA規制医薬品の研究

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米国FDA規制機器製品の研究

いいえ

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