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临床试验/NCT02864524
NCT02864524Unknown不适用

Effects of Manipulative Therapy in the Lower Thoracic and Cervical Spine in Subjects With Fibromyalgia Syndrome

Universidad de Almeria2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2016年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
64
试验地点
2
主要终点
Pain Intensity

研究概览

简要总结

Objective: Compare degree of improvement can reach patients diagnosed with fibromyalgia syndrome, by treatment with Manipulative and Massage Techniques versus an exercise program for lower thoracic and cervical spine.

Study Design: A single-blind randomized controlled trial was conducted on patients with fibromyalgia syndrome (FMS).

Setting: Clinical setting. Methods: Sixty-four subjects with FMS were randomly assigned to an experimental group receiving manipulative and massage therapy, or to a control group for exercise program.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed Fibromyalgia Syndrome.
  • Limitation of usual activities due to pain on at least 1 day in the previous 30 days.
  • Agreement to attend evening therapy sessions.
  • Non-practice of regular physical activity.

排除标准

  • A history of surgery.
  • The presence of comorbid conditions (e.g., morbid obesity, inflammatory diseases, irritable bowel syndrome and interstitial cystitis).
  • A history of whiplash injury.
  • Severe physical disability.
  • Uncontrolled endocrine disorders (e.g., hyperthyroidism, diabetes).
  • Illness (e.g., schizophrenia or substance abuse).
  • The use of medication other than as-needed analgesics (excluding long-term narcotics).
  • Malignancy.
  • Psychiatric disorders.
  • A score of ≥ 9 points in the Beck depression inventory.

结局指标

主要结局

Pain Intensity

时间窗: Changes from Baseline, and 5 weeks

A 10-point numerical scale (0 = no pain, 10: very severe pain)

次要结局

  • Schöber Test(Changes from Baseline, and 5 weeks)
  • Pittsburgh Quality of Life Questionnaire(Changes from Baseline, and 5 weeks)
  • McGill Pain Questionnaire(Changes from Baseline, and 5 weeks)
  • Fatigue Impact Scale (FIS)(Changes from Baseline, and 5 weeks)
  • Quality of Life Questionnaire (SF-36)(Changes from Baseline, and 5 weeks)
  • Fibromyalgia Impact Questionnaire (FIQ)(Changes from Baseline, and 5 weeks)
  • Beck Depression Inventory(Changes from Baseline, and 5 weeks)
  • Pressure Algometry(Changes from Baseline, and 5 weeks)
  • Hospital Anxiety and Depression Scale (HADS)(Changes from Baseline, and 5 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Adelaida María Castro-Sánchez

Professor

Universidad de Almeria

研究点 (2)

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