Shi-style Cervical Manipulations for Nonspecific Neck Pain: a Multi-center, Randomized, Controlled Clinical Trial
25 de outubro de 2021 atualizado por: Cui xuejun, Shanghai University of Traditional Chinese Medicine
Spinal instability diseases have a high prevalence and great harm.
The research on how to prevent and treat degenerative spinal instability diseases has become a hot spot in the international academic community, and it is also an important research content in the field of "population and health" in my country.
Clinical studies have shown that the "Shi-style manipulations" have outstanding efficacy and high safety in the treatment of degenerative spinal instability diseases.
The study intends to carry out a randomized, traction-controlled study in 5 tertiary hospital test centers, with patients with non-specific neck pain as the research object, using "Shi-style manipulations" and traction as intervention methods, and checking indicators and subjective effects through relevant instruments Indicators, quantitative verification of the mechanical parameters and biological effects of the "Shi-style manipulations", scientific evaluation of the efficacy and safety of the "Shi-style manipulations" in non-specific neck pain diseases.
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Intervenção / Tratamento
Descrição detalhada
Spinal diseases are listed as the second most serious diseases in the world's top ten Diseases released by WHO. With the rapid pace of life, the aging of the population and the increase in chronic strain, the incidence of degenerative spinal instability diseases remains high and medical expenses increase.
From 1999 to 2006, 534 patients with various types of degenerative spine instability diseases (except myelomyelitis) were treated by the project team, and the total effective rate of the "three steps and nine steps" in the treatment of clinical symptoms and signs of degenerative spine instability diseases was 91.76%. Through reviewing 60 cases of nerve root type of randomized controlled trials, 8 weeks after treatment, treatment group 30 cases (the whole neck three-step nine method), total effective rate 93.3%, control group total effective rate was 73.3% (cervical traction) (P < 0.01), the treatment group in improving the neck shoulder pain, upper limb numbness, dizziness, tinnitus, brachial plexus pull test is better than that in control group (P < 0.05), the clinical operation without adverse reaction.
Clinical studies have shown that the "Shi-style manipulations" have outstanding efficacy and high safety in the treatment of degenerative spinal instability diseases. The study intends to carry out a randomized, traction-controlled study in 5 tertiary hospital test centers, with patients with non-specific neck pain as the research object, using "Shi-style manipulations" and traction as intervention methods, and checking indicators and subjective effects through relevant instruments Indicators, quantitative verification of the mechanical parameters and biological effects of the "Shi-style manipulations", scientific evaluation of the efficacy and safety of the "Shi-style manipulations" in non-specific neck pain diseases.
Tipo de estudo
Intervencional
Inscrição (Antecipado)
240
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
- Nome: Xuejun Cui, Doctor of Medicine(M.D.)
- Número de telefone: 86-21-64385700
- E-mail: 13917715524@139.com
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
18 anos a 65 anos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:
- The diagnosis is non-specific neck pain;
- Male or female between the ages of 18 and 65 (including 18 and 65);
- VAS score ≥30 mm;
- Sign the informed consent voluntarily.
Exclusion Criteria:
- Have received surgical treatment or neck trauma for cervical spondylosis in the past;
- With cervical nerve compression or spinal cord compression symptoms and signs, MRI found spinal compression;
- The vertebral body was shifted, horizontally shifted >3 mm forward, backward or laterally, and the adjacent intervertebral space had an Angle difference of >11°;
- Patients with liver, kidney, hematopoietic system and other serious primary diseases, with a history of opioid analgesics, sedative and hypnotic drugs and alcohol abuse;
- Patients with osteoporosis, spinal tuberculosis, vertebral body malformation, malignant tumors and mental diseases;
- Pregnant women and lactating women;
- Unable to participate in the follow-up (for example, the plan of migration or long-distance relocation within half a year, no communication tools such as mobile phones, etc.), and the patients without the ability to participate in the half-year follow-up cannot read and write Chinese;
- received radio frequency, minimally invasive, ozone, small needle knife, manipulation, traction or closed treatment Within the last two weeks;
- Participating in other clinical trials related to cervical spondylosis.
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 cruzada
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Comparador Ativo: Traction
6kg to 10kg, 3 times a week, once the other day（except the weekends）,20 minutes, 2 weeks.
|
6kg a 10kg, 3 vezes por semana, uma vez no outro dia (exceto finais de semana), 20 minutos, 2 semanas.
Outros nomes:
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Experimental: Shi-style manipulations
Shi-style manipulations is a cervical manipulation for cervical spondylosis.This manipulation is a kind of traditional Chinese massage and it can dredge the meridians.
Patients are treated every day for 30 minutes.
Seven times as one course and totally there are two courses.
3 times a week, once the other day（except the weekends）,30 minutes, 2 weeks.
|
Shi-style cervical manipulation is a spinal manipulation for cervical radiculopathy.It is a kind of traditional chinese massage and can dredge the meridian.Patients are treated every day for 30 minutes.Seven times at one course and totally there are two courses.3
times a week, once the other day（except the weekends）,30 minutes, 2 weeks.
Outros nomes:
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Musculoskeletal ultrasound
Prazo: changes from baseline at 2 weeks
|
Measure the ratio of the muscle thickness of the back of the neck muscles to the strain rate of the back of the neck muscles.Use real-time dual-frame imaging to adjust the area of interest to ensure coverage of trapezius, supraspinatus, infraspinatus, levator scapula, and sternocleidomastoid.
During operation, the probe lightly touches the ultrasonic coupling patch and is perpendicular to the body surface, hold the probe to slightly vibrate up and down, and keep the pressure release index at 3-4.
Collect the elastic image to ensure that the image is clear and stable for 3-4 seconds.
Observe the elastic image and outline the reference area and the area of interest.
Calculate the SR values of the reference area and the area of interest with the software that comes with the ultrasound system.
Measure 3 times and take the average value.
|
changes from baseline at 2 weeks
|
|
Visual Analogue scale，(VAS)
Prazo: changes from baseline at 2 weeks
|
The visual analog scale is used to measure the patient's current pain level.This scoring ruler has a scale in centimeters on one side, and the smallest scale is millimeters; on the other side, the two ends are marked as "painless" and "most painful".
When using, the researcher holds both ends of the visual analog scale with both hands.
The scale faces the researcher and the non-scale faces the patient.
The patient is asked to use the thumb and index finger to move the upper scale of the ruler to the level of pain.Read the scale value corresponding to the red line of the vernier of the visual analog scale and record it in the research medical record.
The value is rounded to a single digit, and the unit is millimeter (mm).
The red line is between the two scales, and the left value is taken.
Such as "53mm".
|
changes from baseline at 2 weeks
|
|
pressure pain threshold
Prazo: changes from baseline at 2 weeks
|
Determine the corresponding acupoints on the subject's neck, use a round probe to find the pain sensitive points, and mark them with a marker to be measured.
There are 10 points in total.In order to fully relax the tested muscles, supine or lateral positions are used in the measurement.
Before measuring, inform the subject of the entire operation process.The measurement was started after he entered the examination room and rested quietly for 5 minutes.
During the measurement, a tester holds a digital dynamometer, touches the instrument probe vertically downwards to the skin, and applies pressure to the test point at a uniform speed when applying force.
When the subject begins to feel pain, immediately remove the test probe and read the data on the instrument at the same time.
After the measurement is completed, press the zero button to perform the next measurement.
The same acupuncture point was tested 3 times with an interval of 30s, and the average value was taken.
|
changes from baseline at 2 weeks
|
|
Musculoskeletal ultrasound
Prazo: changes from baseline at 1 month
|
Measure the ratio of the muscle thickness of the back of the neck muscles to the strain rate of the back of the neck muscles.Use real-time dual-frame imaging to adjust the area of interest to ensure coverage of trapezius, supraspinatus, infraspinatus, levator scapula, and sternocleidomastoid.
During operation, the probe lightly touches the ultrasonic coupling patch and is perpendicular to the body surface, hold the probe to slightly vibrate up and down, and keep the pressure release index at 3-4.
Collect the elastic image to ensure that the image is clear and stable for 3-4 seconds.
Observe the elastic image and outline the reference area and the area of interest.
Calculate the SR values of the reference area and the area of interest with the software that comes with the ultrasound system.
Measure 3 times and take the average value.
|
changes from baseline at 1 month
|
|
Visual Analogue scale，(VAS)
Prazo: changes from baseline at 1 month
|
The visual analog scale is used to measure the patient's current pain level.This scoring ruler has a scale in centimeters on one side, and the smallest scale is millimeters; on the other side, the two ends are marked as "painless" and "most painful".
When using, the researcher holds both ends of the visual analog scale with both hands.
The scale faces the researcher and the non-scale faces the patient.
The patient is asked to use the thumb and index finger to move the upper scale of the ruler to the level of pain.Read the scale value corresponding to the red line of the vernier of the visual analog scale and record it in the research medical record.
The value is rounded to a single digit, and the unit is millimeter (mm).
The red line is between the two scales, and the left value is taken.
Such as "53mm".
|
changes from baseline at 1 month
|
|
pressure pain threshold
Prazo: changes from baseline at 1 month
|
Determine the corresponding acupoints on the subject's neck, use a round probe to find the pain sensitive points, and mark them with a marker to be measured.
There are 10 points in total.In order to fully relax the tested muscles, supine or lateral positions are used in the measurement.
Before measuring, inform the subject of the entire operation process.The measurement was started after he entered the examination room and rested quietly for 5 minutes.
During the measurement, a tester holds a digital dynamometer, touches the instrument probe vertically downwards to the skin, and applies pressure to the test point at a uniform speed when applying force.
When the subject begins to feel pain, immediately remove the test probe and read the data on the instrument at the same time.
After the measurement is completed, press the zero button to perform the next measurement.
The same acupuncture point was tested 3 times with an interval of 30s, and the average value was taken.
|
changes from baseline at 1 month
|
|
Musculoskeletal ultrasound
Prazo: changes from baseline at 3 months
|
Measure the ratio of the muscle thickness of the back of the neck muscles to the strain rate of the back of the neck muscles.Use real-time dual-frame imaging to adjust the area of interest to ensure coverage of trapezius, supraspinatus, infraspinatus, levator scapula, and sternocleidomastoid.
During operation, the probe lightly touches the ultrasonic coupling patch and is perpendicular to the body surface, hold the probe to slightly vibrate up and down, and keep the pressure release index at 3-4.
Collect the elastic image to ensure that the image is clear and stable for 3-4 seconds.
Observe the elastic image and outline the reference area and the area of interest.
Calculate the SR values of the reference area and the area of interest with the software that comes with the ultrasound system.
Measure 3 times and take the average value.
|
changes from baseline at 3 months
|
|
Visual Analogue scale，(VAS)
Prazo: changes from baseline at 3 months
|
The visual analog scale is used to measure the patient's current pain level.This scoring ruler has a scale in centimeters on one side, and the smallest scale is millimeters; on the other side, the two ends are marked as "painless" and "most painful".
When using, the researcher holds both ends of the visual analog scale with both hands.
The scale faces the researcher and the non-scale faces the patient.
The patient is asked to use the thumb and index finger to move the upper scale of the ruler to the level of pain.Read the scale value corresponding to the red line of the vernier of the visual analog scale and record it in the research medical record.
The value is rounded to a single digit, and the unit is millimeter (mm).
The red line is between the two scales, and the left value is taken.
Such as "53mm".
|
changes from baseline at 3 months
|
|
pressure pain threshold
Prazo: changes from baseline at 3 months
|
Determine the corresponding acupoints on the subject's neck, use a round probe to find the pain sensitive points, and mark them with a marker to be measured.
There are 10 points in total.In order to fully relax the tested muscles, supine or lateral positions are used in the measurement.
Before measuring, inform the subject of the entire operation process.The measurement was started after he entered the examination room and rested quietly for 5 minutes.
During the measurement, a tester holds a digital dynamometer, touches the instrument probe vertically downwards to the skin, and applies pressure to the test point at a uniform speed when applying force.
When the subject begins to feel pain, immediately remove the test probe and read the data on the instrument at the same time.
After the measurement is completed, press the zero button to perform the next measurement.
The same acupuncture point was tested 3 times with an interval of 30s, and the average value was taken.
|
changes from baseline at 3 months
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Neck Disabilitv Index， (NDI)
Prazo: changes from baseline at 2 weeks
|
The Neck Disability Index (NDI) is one of the most frequently used questionnaires in clinical practice.
The questionnaire mainly assesses the patient's pain level, self-care ability, weightlifting, reading, headache level, concentration, work, driving, sleep, and entertainment.
It quantifies the points of all aspects, and the score ranges from 0 points (no disability) to 5 points (completely disabled), the total score ranges from 0 points (no disability) to 50 points (completely disabled), for a total of 50 points.
The lower the total score, the less severe the patient's condition, and vice versa.
|
changes from baseline at 2 weeks
|
|
the MOS item short from health survey，(SF-36)
Prazo: changes from baseline at 2 weeks
|
The SF-36 scale is a universal scale developed by the American Medical Research Group to measure the quality of life, and is universally recognized and widely used in the world.
This scale has a total of 8 dimensions to evaluate health-related quality of life (HRQOL), which is divided into two categories: physical health and mental health, namely physical function (PF), physical function (RP), physical pain (BP), and general health (CH), Activity (VT), Social Function (SF), Emotional Function (RE), Mental Health (MH).
|
changes from baseline at 2 weeks
|
|
Cervical range of motion
Prazo: changes from baseline at 2 weeks
|
Measure the range of cervical spine flexion, extension, lateral flexion, and rotation by using a universal protractor
|
changes from baseline at 2 weeks
|
|
Neck Disabilitv Index， (NDI)
Prazo: changes from baseline at 1 month
|
The Neck Disability Index (NDI) is one of the most frequently used questionnaires in clinical practice.
The questionnaire mainly assesses the patient's pain level, self-care ability, weightlifting, reading, headache level, concentration, work, driving, sleep, and entertainment.
It quantifies the points of all aspects, and the score ranges from 0 points (no disability) to 5 points (completely disabled), the total score ranges from 0 points (no disability) to 50 points (completely disabled), for a total of 50 points.
The lower the total score, the less severe the patient's condition, and vice versa.
|
changes from baseline at 1 month
|
|
the MOS item short from health survey，(SF-36)
Prazo: changes from baseline at 1 month
|
The SF-36 scale is a universal scale developed by the American Medical Research Group to measure the quality of life, and is universally recognized and widely used in the world.
This scale has a total of 8 dimensions to evaluate health-related quality of life (HRQOL), which is divided into two categories: physical health and mental health, namely physical function (PF), physical function (RP), physical pain (BP), and general health (CH), Activity (VT), Social Function (SF), Emotional Function (RE), Mental Health (MH).
|
changes from baseline at 1 month
|
|
Cervical range of motion
Prazo: changes from baseline at 1 month
|
Measure the range of cervical spine flexion, extension, lateral flexion, and rotation by using a universal protractor
|
changes from baseline at 1 month
|
|
Neck Disabilitv Index， (NDI)
Prazo: changes from baseline at 3 months
|
The Neck Disability Index (NDI) is one of the most frequently used questionnaires in clinical practice.
The questionnaire mainly assesses the patient's pain level, self-care ability, weightlifting, reading, headache level, concentration, work, driving, sleep, and entertainment.
It quantifies the points of all aspects, and the score ranges from 0 points (no disability) to 5 points (completely disabled), the total score ranges from 0 points (no disability) to 50 points (completely disabled), for a total of 50 points.
The lower the total score, the less severe the patient's condition, and vice versa.
|
changes from baseline at 3 months
|
|
the MOS item short from health survey，(SF-36)
Prazo: changes from baseline at 3 months
|
The SF-36 scale is a universal scale developed by the American Medical Research Group to measure the quality of life, and is universally recognized and widely used in the world.
This scale has a total of 8 dimensions to evaluate health-related quality of life (HRQOL), which is divided into two categories: physical health and mental health, namely physical function (PF), physical function (RP), physical pain (BP), and general health (CH), Activity (VT), Social Function (SF), Emotional Function (RE), Mental Health (MH).
|
changes from baseline at 3 months
|
|
Cervical range of motion
Prazo: changes from baseline at 3 months
|
Measure the range of cervical spine flexion, extension, lateral flexion, and rotation by using a universal protractor
|
changes from baseline at 3 months
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
The doctor of traditional Chinese medicine syndrome
Prazo: changes from baseline at 2 weeks
|
The TCM Syndrome Feature Scale is based on the patient's general symptoms, signs (including tongue and pulse), physical examination, and laboratory examination results to establish an information table, and then use the difference matrix method to perform attribute reduction and case reduction to obtain The lower approximation set and the upper approximation set are used to extract the definite rules and possible rules of TCM diagnosis.
In this way, the subjectivity and one-sidedness of doctors are avoided to a large extent, making TCM syndrome diagnosis and treatment more standardized and scientific
|
changes from baseline at 2 weeks
|
|
The doctor of traditional Chinese medicine syndrome
Prazo: changes from baseline at 1 month
|
The TCM Syndrome Feature Scale is based on the patient's general symptoms, signs (including tongue and pulse), physical examination, and laboratory examination results to establish an information table, and then use the difference matrix method to perform attribute reduction and case reduction to obtain The lower approximation set and the upper approximation set are used to extract the definite rules and possible rules of TCM diagnosis.
In this way, the subjectivity and one-sidedness of doctors are avoided to a large extent, making TCM syndrome diagnosis and treatment more standardized and scientific
|
changes from baseline at 1 month
|
|
The doctor of traditional Chinese medicine syndrome
Prazo: changes from baseline at 3 months
|
The TCM Syndrome Feature Scale is based on the patient's general symptoms, signs (including tongue and pulse), physical examination, and laboratory examination results to establish an information table, and then use the difference matrix method to perform attribute reduction and case reduction to obtain The lower approximation set and the upper approximation set are used to extract the definite rules and possible rules of TCM diagnosis.
In this way, the subjectivity and one-sidedness of doctors are avoided to a large extent, making TCM syndrome diagnosis and treatment more standardized and scientific
|
changes from baseline at 3 months
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Yongjun Wan, Doctor of Medicine(M.D.), Shanghai University of Traditional Chinese Medicine
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 (Antecipado)
1 de novembro de 2021
Conclusão Primária (Antecipado)
30 de dezembro de 2022
Conclusão do estudo (Antecipado)
30 de dezembro de 2022
Datas de inscrição no estudo
Enviado pela primeira vez
25 de outubro de 2021
Enviado pela primeira vez que atendeu aos critérios de CQ
25 de outubro de 2021
Primeira postagem (Real)
5 de novembro de 2021
Atualizações de registro de estudo
Última Atualização Postada (Real)
5 de novembro de 2021
Última atualização enviada que atendeu aos critérios de controle de qualidade
25 de outubro de 2021
Última verificação
1 de outubro de 2021
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- Nonspecific Neck Pain
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
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 .