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临床试验/NCT04815915
NCT04815915已完成不适用

Effects of Graston Technique in Patients With Non Specific Low Back Pain

Riphah International University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2020年4月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
1
主要终点
PNRS

研究概览

简要总结

Non-specific low back pain upsets individuals of all age gathering and is a most significant provider to illness load everywhere on the world. Overseeing rules prescribe emergency to locate the uncommon instances of low back pain that are brought about by actually genuine pathology, thus need demonstrative work-up or proficient arrangement, or both. Since non-specific low back pain doesn't have a known pathoanatomical cause and treatment accentuations on diminishing in agony and its meanings.

To determine the impacts of Graston technique in patients with non-specific low back pain.

This examination was Quasi Experimental study and on the basis of inclusion standards, 20 patients were involved. PNRS and ODI used to collect the data. Graston tool was used to treat patients 3 times in a week according protocol for 6 weeks' treatment plan with extensions bised exercises protocol following pattern of APTA. The data was analyzed using SPSS 21.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •• Both genders
  • •Age (20-40 years)
  • •Patients with non-specific backache
  • •Trigger points and tender points at low back region

排除标准

  • •• Patients with chronic diseases
  • •Degenerative changes in spine
  • •Open wounds around the area to be treated
  • •High blood pressure
  • •Diabetic neuropathy
  • •Cancer (depending on the type and location)
  • •Taking anti-coagulants
  • •Pregnancy

研究组 & 干预措施

Study Group

Experimental

Graston tool was used to treat patients 3 times in a week according protocol for 6 weeks' treatment plan with extensions bised exercises protocol following pattern of APTA.

干预措施: Graston technique (Other)

结局指标

主要结局

PNRS

时间窗: 2 months

Pain Numeric Rating Scale (PNRS) scores in subjects with moderate/severe pain at baseline. \*P \< 0.0001 vs. baseline. Includes only subjects with baseline PNRS score of 4 to 10. Scale ranges from 0 to 10. Data are shown as mean ± 95% confidence interval. n = 329 for all visits, all with a baseline PNRS score of 4 to 10.

OSWESTRY DISABILITY INDEX

时间窗: 2 months

Each section is scored on a 0-5 scale, 5 representing the greatest disability. The index is calculated by dividing the summed score by the total possible score, which is then multiplied by 100 and expressed as a percentage. Thus, for every question not answered, the denominator is reduced by 5

次要结局

未报告次要终点

研究者

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

Maryam Shabbir

Associate Professor

Riphah International University

研究点 (1)

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