Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Sensory Motor Control and Muscle Energy Technique for Chronic Mechanical Neck

26 de junho de 2026 atualizado por: 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

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

52

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

      • Islamabad, Paquistão
        • Recrutamento
        • Max Spine Rehab Center, Max Health Hospital
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

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

-

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Diagnóstico
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de Placebo: 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.
Experimental: 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

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
NPRS
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
NDI
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de janeiro de 2026

Conclusão Primária (Estimado)

15 de agosto de 2026

Conclusão do estudo (Estimado)

1 de setembro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

26 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

26 de junho de 2026

Primeira postagem (Real)

2 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

2 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

26 de junho de 2026

Última verificação

1 de janeiro de 2026

Mais Informações

Termos relacionados a este estudo

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever