Impact of Manual Therapy on the Coxofemoral Joint in Patients With Chronic Low Back Pain of Non-Specific Origin.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Changes in Pain
研究概览
简要总结
The study will be carried out at the Faculty of Nursing and Physiotherapy of the University of Alcalá. The study has been approved by the Animal Research and Experimentation Ethics Committee of the University of Alcalá. A total of 60 subjects aged between 18 and 35 with non.specific low back pain will be selected and randomized in two interventions.
The control group will carry out a specific strengthening program for the gluteus maximus and the experimental group will carry out the same strengthening program in addition to receiving a specific manual therapy program for both hips.
The total duration of the treatments will be 8 weeks, with on-treatment evaluations at 4 and 8 weeks, with a follow-up after 1 month.
The objective will be to determine the efficacy of manual therapy on the coxofemoral joint together with a protocol of gluteus maximus strengthening exercises in patients with non-specific chronic low back pain, in comparison with the same protocol of gluteus maximus strengthening exercises performed in isolation, in patients with non-specific chronic low back pain.
详细描述
Detailed Description has not been entered.
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 35 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with non-specific low back pain, with a score of more than 2 on the visual analogue scale.
- •Pain with a course of more than 12 weeks, of a chronic nature.
排除标准
- •Patients with neurological signs and symptoms or severe psychiatric illnesses.
- •Subjects with a history of severe trauma, fracture or previous surgery on the lumbar spine or hip.
- •Subjects with a history of musculoskeletal and/or rheumatologic disease.
- •Patients with low back pain attributable to dysmenorrhoea.
- •Pregnant patients.
- •Individuals with fibromyalgia, autoimmune disorders.
- •Subjects with a history of oncological processes.
结局指标
主要结局
Changes in Pain
时间窗: Baseline, 4 weeks, 8weeks, 1 month after intervention commencement
measured with visual analogic scale A straight horizontal line of fixed length, usually 100 mm is drawn. The ends are defined as the extreme limits of the parameter to be measured (pain) orientated from the left (worst) to the right (best).
次要结局
- Changes in Depression(Baseline, 4 weeks, 8weeks, 1 month after intervention commencement)
- Changes in Disability(Baseline, 4 weeks, 8weeks, 1 month after intervention commencement)
- Changes in the Range of Motion of the Hip Joint(Baseline, 4 weeks, 8weeks, 1 month after intervention commencement)
- Changes in Health related quality of life(Baseline, 4 weeks, 8weeks, 1 month after intervention commencement)
- Changes in Gluteus Maximus Strength(Baseline, 4 weeks, 8weeks, 1 month after intervention commencement)
研究者
Alexander Achalandabaso
Principal investigator
University of Jaén