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Effects of Mulligan Belt Traction Versus Fisted Traction in Patients With Lower Cervical Spine Radiculopathy

1 de junho de 2026 atualizado por: Riphah International University

Effects of Mulligan Belt Traction Versus Fisted Traction on Pain, Range of Motion and Disability Level in Patients With Lower Cervical Spine Radiculopathy

Individuals with a lower cervical spine radiculopathy diagnosis will undergo screening to determine their eligibility based on inclusion and exclusion criteria. Eligible participants will be asked for their informed consent

Visão geral do estudo

Status

Ativo, não recrutando

Descrição detalhada

Participants will receive a unique identifying code to maintain confidentiality and be formally enrolled in the study upon obtaining informed consent. Following that, they will have baseline evaluations for outcome factors such as neck disability index, range of motion using goniometry and pain using a numerical pain rating scale. After completing the baseline evaluation, participants will be divided into two groups: Group A will receive a Mulligan Belt Traction, while Group B will receive a Fisted Traction. Every participant will get treatment for four weeks, with three sessions per week. At the conclusion of the intervention period, a post-intervention assessment will be carried out Randomization:Random allocation of participants into the two groups, Group A and Group B, will be performed by a lottery method. The participants of Group A will be managed by Mulligan Belt Traction while in Group B, participants will receive Fisted Traction. The physiotherapists will provide both interventions during a specified time period.

Tipo de estudo

Intervencional

Inscrição (Real)

44

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.

Locais de estudo

    • Punjab Province
      • Lahore, Punjab Province, Paquistão, 54000

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:• Age 25-60 years

  • Both Male and Female
  • Clinically or radiologically diagnosed lower cervical radiculopathy(C5-C7)
  • Neck pain radiating to the arm and hand
  • Positive Spurling's Test or Upper Limb Tension test
  • Subacute to chronic phase (>4 weeks to 6< weeks)
  • Moderate pain (VAS> 4/10)
  • Evident by a score on Neck Disability Index (NDI >20%)
  • Able and willing to give informed consent and follow the protocol
  • Cervical spine active range of motion (CSAROM) Exclusion Criteria:• Cervical Fracture
  • Thoracic outlet syndrome or carpal tunnel syndrome
  • History of previous cervical surgery
  • Osteoporosis of cervical spine
  • Sign of myelopathy
  • Severe cervical disc herniation with cord compression
  • Red flag signs (Rheumatoid arthritis, history of trauma, ankylosing spondylitis, prolonged steroid used and malignancy

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: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: conventional group
Conventional physiotherapy which include cervical traction, hot pack and isometric strengthening exercises for lower cervical radiculopathy

Patient Position:

  • The Patient lies supine on the treatment table.
  • Head in neutral or slightly flexed position (according to comfort and symptoms).
  • Arms rest by the sides.

Therapist Position:

  • Therapist stands at the head end of table, therapist places the middle finger on the concerned cervical segment.
  • To maintain joint contact and control movement at the level.

Belt Placement:

  • The Mulligan belt is positioned at an angle to apply gentle traction targeting the lower cervical spine (C5-C7) (16)
  • Make sure there is no pressure on the throat or jaw.

Application of Traction:

  • While maintaining contact at the target segment, therapist leans backward, to apply gentle sustained and controlled traction (distraction force) along the line of the cervical spine.
  • This help to open up the intervertebral foramen, reduce nerve compression and restore normal joint mechanics. (17)

Duration:

• Traction is applied for 10-30 seconds per repetition, repeated 3-5 times per session base

Sit upright in a chair with back support.

• Keep your spine straight and head in a neutral position.

Hand Placement:

  • One fist is placed at the upper chest\sternum, acting as a fulcrum.
  • A towel is used between the fist and chest for comfort and positioning.(18)
  • The opposite hand is placed around the back of head (occiput).

Traction Technique:

  • The head is pulled forward and down, guiding cervical flexion over the fist.
  • Maintain for 10-15 seconds, repeat 5-10 times, depending on comfort.
Comparador Ativo: conventional therapy
Conventional physiotherapy which include cervical traction, hot pack and isometric strengthening exercises for lower cervical radiculopathy

Patient Position:

  • The Patient lies supine on the treatment table.
  • Head in neutral or slightly flexed position (according to comfort and symptoms).
  • Arms rest by the sides.

Therapist Position:

  • Therapist stands at the head end of table, therapist places the middle finger on the concerned cervical segment.
  • To maintain joint contact and control movement at the level.

Belt Placement:

  • The Mulligan belt is positioned at an angle to apply gentle traction targeting the lower cervical spine (C5-C7) (16)
  • Make sure there is no pressure on the throat or jaw.

Application of Traction:

  • While maintaining contact at the target segment, therapist leans backward, to apply gentle sustained and controlled traction (distraction force) along the line of the cervical spine.
  • This help to open up the intervertebral foramen, reduce nerve compression and restore normal joint mechanics. (17)

Duration:

• Traction is applied for 10-30 seconds per repetition, repeated 3-5 times per session base

Sit upright in a chair with back support.

• Keep your spine straight and head in a neutral position.

Hand Placement:

  • One fist is placed at the upper chest\sternum, acting as a fulcrum.
  • A towel is used between the fist and chest for comfort and positioning.(18)
  • The opposite hand is placed around the back of head (occiput).

Traction Technique:

  • The head is pulled forward and down, guiding cervical flexion over the fist.
  • Maintain for 10-15 seconds, repeat 5-10 times, depending on comfort.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Neck Disability Index
Prazo: baseline to 4 week
The NDI contains 10 items - 7 relating to activities of daily living, 2 relating to pain and 1 relating to concentration items is scored from 0-5, and the total score is expressed as a percentage (total possible score, 100%), with higher scores corresponding to greater disability. Scoring the NDI: 0 - 4 = No disability 5 - 14 = Mild disability 15 - 24 = Moderate disability 25 - 34 = Severe disability 35 or over = Complete disability
baseline to 4 week
Numeric pain rating scale
Prazo: baseline to 4 week
The NPRS is a reliable and effective tool for measuring pain. A straight line is drawn on the evaluation sheet, labeled from '0' to '10', where '0' represents no pain and '10' indicates the worst possible pain. Patients are asked to mark a point on the line that reflects the intensity of pain they are experiencing at the time of assessment
baseline to 4 week
Cervical Range of Motion
Prazo: baseline to 4 week

Cervical Flexion (Looking Down) Position: The patient sits upright. Goniometer Axis: Placed at the external auditory meatus (ear). Stationary Arm: Kept perpendicular to the floor. Moving Arm: Aligned with the base of the nose. Normal Range: 0 to 45 degrees 2 Cervical Extension (Looking Up) Position: Patient remains seated upright. Goniometer Axis: Centered at the external auditory meatus. Stationary Arm: Vertical, perpendicular to the floor. Moving Arm: Follows the line of the nose. Normal Range: 0 to 45 degrees

3. Cervical Lateral Flexion (Side Bending) Position: Patient sits straight. Goniometer Axis: Over the C7 spinous process. Stationary Arm: Aligned vertically along the spine. Moving Arm: Follows the midline of the head toward the occipital bone. Normal Range: 0 to 45 degrees 4.Cervical Rotation (Turning Head Side to Side) Position: Patient remains upright. Goniometer Axis: Placed at the top center of the head. Stationary Arm: Imaginary line between both shoulder tips.

baseline to 4 week

Colaboradores e Investigadores

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Publicações e links úteis

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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)

2 de julho de 2025

Conclusão Primária (Estimado)

6 de agosto de 2026

Conclusão do estudo (Estimado)

4 de setembro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

1 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de junho de 2026

Primeira postagem (Real)

5 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

5 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

nill

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 .

Ensaios clínicos em Radiculopatia Cervical

Ensaios clínicos em muligan belt traction

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