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临床试验/CTRI/2024/05/068081
CTRI/2024/05/068081已完成2 期

Effect of Graded Sensorimotor Retraining on pain, kinesophobia and postural stability among young adults with non-specific chronic low back pain: A Randomised Controlled Trial

Nitte Instituteof Physiotherapy1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
56
试验地点
1
主要终点
1) Numerical Pain Rating Scale

研究概览

简要总结

In recent scenario,it is estimated that up to 85% of people with low back pain (LBP) who seek primary care are non-specific and major population affected by it is young adults. It has been noted that standard care is effective in treating the condition for a particular period  when it comes to recurrent bouts of low back pain. In addition to the goal of reducing pain, postural stability and kinesophobia should be taken into account when treating chronic non-specific low back pain.  A multi-modal strategy i.e. graded sensorimotor retraining which includes retraining the brain’s motor and sensory regions helps in not only reduction of pain but also resolve kinesophobia and increases postural stability. The graded approach used in this specific treatment helps to retrain both the aspects. So, this study is proposed to identify the effectiveness of including sensory as well as motor aspect while treating non-specific chronic low back pain.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 28.00 Year(s)(—)
性别
All

入选标准

  • Students who are 18 to 28 years of age 2)Both male & female 3)Chronic low back pain of a non-specific nature 4)Young individuals suffering from at least a single episode of back pain in the past 3 months 5)NPRS ( Numerical Pain Rating Scale) score between 3 out of 10 to 8 outof 10.

排除标准

  • Presence of neurological signs (e.g., perceived weakness in the lower limbs) 2)A diagnosed psychiatric disorder or severe cognitive impairment 3)Having the specific disease (e.g., malignancy, inflammatory joint and bone disease).

结局指标

主要结局

1) Numerical Pain Rating Scale

时间窗: Once the individual is included in the study, readings will be taken as baseline values and after 8 weeks of treatment.

2) TAMPA scale for kinesophobia

时间窗: Once the individual is included in the study, readings will be taken as baseline values and after 8 weeks of treatment.

3) Multidirectional functional reach test

时间窗: Once the individual is included in the study, readings will be taken as baseline values and after 8 weeks of treatment.

次要结局

未报告次要终点

研究者

发起方
Nitte Instituteof Physiotherapy
申办方类型
Other [Nitte Institute of Physiotherapy NITTE (Deemed to be university)]
责任方
Principal Investigator
主要研究者

Sable Kruti Prakash

Nitte Institute of Physiotherapy NITTE (Deemed to be university)

研究点 (1)

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