跳至主要内容
临床试验/CTRI/2024/04/065751
CTRI/2024/04/065751尚未招募不适用

Efficacy of cyriax therapy on pain, lumbar strength and joint position sense in individual’s with chronic low back pain

nManav Rachna International Institute of Research And Studies1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年4月24日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
36
试验地点
1
主要终点
1. VAS- Pain

研究概览

简要总结

This study will be conducted in the department of physiotherapy, Manav Rachna International University of Research and Studies in Haryana. Study details and risks will be explained to all the participants and they will voluntarily participate in the study by signing the consent form after the initial assessment and screening through the selection criteria.

The subjects will be divided into 2 groups by using convenient sampling techniques.

Group A- Control group (Conventional group). while the controlled group will undergo standard treatments for chronic low back pain with selective exercises and hot pack, TENS.

Group B - Experimental group (Cyriax Therapy group). The Cyriax Therapy group will receive manual therapy sessions based on the Cyriax approach( DTFM, Stretching and Mobilization),and Selective Exercises.

Treatment will be given 4 times/week for 4 weeks duration in both the groups.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
20.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • History of chronic pain ≥ 12 weeks
  • With or without Radiating pain 3.

排除标准

  • Recurrent low back pain
  • Neurological, Psycho-cognitive and Psychosomatic disorders
  • Any previous history of fracture in the spine or lower limb, muscular degenerative disorder
  • cardiopulmonary or endocrine disorders with contraindication to physical exercise
  • Any previous history of systemic infection.

结局指标

主要结局

1. VAS- Pain

时间窗: 1. Baseline (Day 0) | 2. Post intervention-1 (after two weeks) day 14 | 3. Post intervention -II (after 4 weeks) day 28

2. Goniometer – range of motion for lower limbs and lumber region

时间窗: 1. Baseline (Day 0) | 2. Post intervention-1 (after two weeks) day 14 | 3. Post intervention -II (after 4 weeks) day 28

3. MMT- for lower back and lower limb Strength

时间窗: 1. Baseline (Day 0) | 2. Post intervention-1 (after two weeks) day 14 | 3. Post intervention -II (after 4 weeks) day 28

4. Lumbar joint position sense (LJPS)- For joint position sense

时间窗: 1. Baseline (Day 0) | 2. Post intervention-1 (after two weeks) day 14 | 3. Post intervention -II (after 4 weeks) day 28

次要结局

  • 1. Oswestry disability scale- for quality of life(2. Tampa Scale for Kinesiophobia(TSK)- For fear of movement)

研究者

发起方
nManav Rachna International Institute of Research And Studies
申办方类型
Other [Private institute]
责任方
Principal Investigator
主要研究者

Paramananda Roy

Manav rachna international institute of research and studies

研究点 (1)

Loading locations...

相似试验