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Набор скоро начнётся NCT07522710

Clinical Study on Intensive Multi-acupuncture in the Treatment of Neck and Shoulder Myofascial Pain Syndrome

Без фазы С лечением Neck Pain Shoulder and Neck

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Acupuncture, Acupuncture.
Кому может быть актуально
Состояния в реестре: Neck Pain, Shoulder and Neck. Базовые параметры: 18 лет — 69 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

Clinical Study on the Treatment of Neck and Shoulder Pain by Intensive Multi-acupuncture Method Based on the Principle of "Tendons Disease Pain-point Needling".

Обзор

In this study, the proposed subjects came from the Traditional Diagnosisand Treatment Center of Zhongshan Hospital of Zhejiang Province.78 patients with neck and shoulder pain who met the criteria were randomly divided into the control group (39 cases) and the experimental group (39 cases) in a ratio of 1:1.The control group used ordinary acupuncture methods,and the experimental group adopted intensive mtlti-acupuncture method for intervention.The treatment was carried out twice a week,with 4 times as a course of treatment,for a total of one couse of treatment. The data of VAS NDI,Cervical Range of Motion Assessment,and Constant-Murley Score of the two grous were recorded at the baseline period,after the 2nd treatment,after the 4th treatment,and 2 weeks after the end of the treatment for follow-up.All data were statistically analyzed using SPSS27.0 software,and relevant differences were compared after treatment. In order to evaluate the effectiveness of intensive multi-acupuncture method in the treatment of neck and shoulder pain,and to promote the development and clinical application of"pain as adupoint" meridian stabbing method.

Вмешательства

  • Процедура Acupuncture
    The needles are inserted into the subject body to treat the disease.
  • Процедура Acupuncture
    The needles are inserted into the subject body to treat the disease.

Первичные конечные точки

  • clinical efficacy evaluation criteria [Срок оценки: Through study completion, an average of 1 year]
Вторичные конечные точки (4)
  • Pain visual analog scale score(VAS) [Срок оценки: Through study completion, an average of 1 year]
  • Neck Disability Index (NDI) score [Срок оценки: Through study completion, an average of 1 year]
  • Cervical Range of Motion (CROM) scale [Срок оценки: Through study completion, an average of 1 year]
  • Constant-Murley Score (CMS) scale [Срок оценки: Through study completion, an average of 1 year]

Критерии участия

Критерии включения

  • Meet the above diagnostic criteria for both Chinese and Western medicine;
  • Aged between 18 and 69 years, with no gender restriction; ③ Disease duration of more than 3 months, with no other treatment received within the past month; ④ Voluntarily participate in this study, comply with the physician's arrangements, cooperate with treatment, and sign the Informed Consent Form.

Критерии исключения

  • Patients with severe life-threatening primary diseases such as severe cardiac, hepatic, renal, or hematopoietic system disorders, as well as those with psychiatric conditions;
  • Patients with pre-existing diseases that may affect the diagnosis of this condition, such as spinal cord injury, significant cervical disc herniation or spondylolisthesis, cervical compression fracture, whiplash injury, etc., as well as those complicated by visceral disorders presenting with similar symptoms; ③ Women who are pregnant or breastfeeding, for whom acupuncture treatment is not suitable;
  • Patients with a history of needle phobia, hemophobia, bleeding tendency, or coagulation disorders;
  • Patients with ulcers or suspected infection on the local body surface; ⑥ Patients who have received other treatments within the past two weeks that may potentially affect the observation of the study outcomes; ⑦ Patients with cognitive impairments who are unable to independently complete the relevant scale assessments or do so under the guidance of the researcher.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07522710 · ZSLL-ZN-2026-008-01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗