Shi-style Cervical Manipulations for Nonspecific Neck Pain: a Multi-center, Randomized, Controlled Clinical Trial
2021年10月25日 更新者：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.
調査の概要
詳細な説明
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.
研究の種類
介入
入学 (予想される)
240
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
- 名前：Xuejun Cui, Doctor of Medicine(M.D.)
- 電話番号：86-21-64385700
- メール：13917715524@139.com
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
18年～65年 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
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.
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：処理
- 割り当て：ランダム化
- 介入モデル：クロスオーバー割り当て
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ：Traction
6kg to 10kg, 3 times a week, once the other day（except the weekends）,20 minutes, 2 weeks.
|
6kg～10kg、週3回、隔日1回（土日除く）、20分、2週間。
他の名前：
|
|
実験的：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.
他の名前：
|
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 |
|---|---|---|
|
Musculoskeletal ultrasound
時間枠：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)
時間枠：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
時間枠：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
時間枠：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)
時間枠：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
時間枠：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
時間枠：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)
時間枠：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
時間枠：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
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Neck Disabilitv Index， (NDI)
時間枠：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)
時間枠：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
時間枠：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)
時間枠：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)
時間枠：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
時間枠：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)
時間枠：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)
時間枠：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
時間枠：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
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The doctor of traditional Chinese medicine syndrome
時間枠：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
時間枠：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
時間枠：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
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
協力者
捜査官
- 主任研究者：Yongjun Wan, Doctor of Medicine(M.D.)、Shanghai University of Traditional Chinese Medicine
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 (予想される)
2021年11月1日
一次修了 (予想される)
2022年12月30日
研究の完了 (予想される)
2022年12月30日
試験登録日
最初に提出
2021年10月25日
QC基準を満たした最初の提出物
2021年10月25日
最初の投稿 (実際)
2021年11月5日
学習記録の更新
投稿された最後の更新 (実際)
2021年11月5日
QC基準を満たした最後の更新が送信されました
2021年10月25日
最終確認日
2021年10月1日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- Nonspecific Neck Pain
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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Dexa Medica Group完了
頸部牽引制御の臨床試験
-
ReVivo Medical, Corp.The Cleveland Clinic; Albany Medical College; IGEA募集首の痛み | 脊椎症 | ミエロパシーを伴う脊椎症 | 神経根症を伴う脊椎症 | 神経根症を伴う脊椎症 頸部領域 | 椎間板障害 子宮頸部アメリカ
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Indiana UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)募集
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University of Southern MississippiMilitary Suicide Research Consortium招待による登録
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University of British ColumbiaUniversity of Victoria; Social Sciences and Humanities Research Council of Canada完了
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Johns Hopkins UniversityNational Institute on Deafness and Other Communication Disorders (NIDCD); GN Otometrics完了
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Devicare S.L.Clever Instruments S.L.; Fundacio Puigvertわからない
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W.L.Gore & Associates完了胸部疾患スウェーデン, オランダ, スペイン, ドイツ, フランス, イギリス, イタリア