Effectiveness of Massage Therapy With Active Component and Therapeutic Exercise in Cervical Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 42
- 试验地点
- 2
- 主要终点
- Change in Neck disability
研究概览
简要总结
It is an interventional study that proves the eficacy of the manual therapy with active manual therapy and combined with exercise in cervical pain.
详细描述
The study will be divided in two different groups:
- A control group (group A) : they will receive a treatment with manual therapy and physical exercise.
- An experimental group (group B) : they will receive the previous treatment, but also the pacient's do active muscle active contraction.
The exercise is compound by a home program of several exercises with diferent difficulties.
The contraction will consist on a combination of concentric and isometric work. being the patient's pain threshold the one that will guide us to the choice of the predominance of concentric or isometric contraction . Both groups will be joined by a five-minute work on pain education.
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 (Participant)
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •accept to participate in the study, through informed consent
- •subjects with chronic nonspecific neck pain lasting equal to or more than 3 months
排除标准
- •Present neck pain caused by serious pathology such as: inflammatory, congenital, infectious, metabolic and neoplastic diseases.
- •Cervical pathology of traumatic origin with less than 6 months of evolution.
- •Rheumatic diseases.
- •Neck pain with neurological signs such as: radiculopathy and myelopathy.
- •Previous surgery of the cervical spine.
- •Pregnancy.
- •Have received physiotherapeutic treatment in the cervical region during the month prior to the inclusion of the study.
- •Have the intention of receiving other physiotherapeutic treatments different from the one proposed during the study period.
- •Present serious mental disorders.
结局指标
主要结局
Change in Neck disability
时间窗: Baseline, 1 month (primary timepoint) , 2 months and 5 months after intervention commencement.
Using the Neck Disability Index (NDI). It is made up of 10 items and each item is scored on a 6-point Likert scale (0 to 5), leading to a total score ranging from 0 to 50 (0 to 4 = no disability; 5 to 14 = mild disability; 15 to 24 = moderate disability; 25 to 34 = severe disability; and 35 to 50 = complete disability).
次要结局
- Change in pain perception(Baseline, 1 month (primary timepoint), 2 months and 5 months after intervention commencement.)
- Change in Range of motion (ROM)(Baseline, 1 month (primary timepoint) and 2 months after intervention commencement.)
- Change in kinesophobia(Baseline, 1 month (primary timepoint) , 2 months and 5 months after intervention commencement.)
- Change in Catastrophism(Baseline, 1 month (primary timepoint), 2 months and 5 months after intervention commencement.)
- Change in Sleep Quality(Baseline, 1 month (primary timepoint) , 2 months and 5 months after intervention commencement.)
- Change in craniocervical flexion(Baseline, 1 month (primary timepoint) and 2 months after intervention commencement.)
研究者
Alexander Achalandabaso
Physiotherapy doctor
University of Jaén