跳至主要内容
临床试验/CTRI/2025/02/080892
CTRI/2025/02/080892尚未招募2/3 期

CLINICAL EVALUATION OF EFFECTIVENESS OF UDVARTANA IN MANAGING PAIN INDUCED DUE TO VYAYAM IN STHULA(OVERWEIGHT/OBESE).

Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年3月1日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
1. To study the effectiveness of udvartana in preventing pain given before vyayama on subjects with pain induced due to vyayama.

研究概览

简要总结

CLINICAL EVALUATION OF EFFECTIVENESS OF UDVARTANA IN MANAGING PAIN INDUCED DUE TO VYAYAMA IN STHULA*.*** A 5 days clinical trail with 40 patients. 20 in each group namely study group and comparative group. Patients diagnosed using BMI, Brocas index and Waist hip ratio filtered after inclusion and exclusion criteria will be selected for the study. Intervention include an external procedure named Udavartana given before vyayama in one group and after vyayama in other.  Pain induced due to vyayama and after udvatana will be assessed  using Defense and Veterans Pain Rating Scale and Likert scale for muscle soreness and noted. The date with be then analysed using statistical software.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

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

入选标准

  • Subjects with BMI 23 to 39.9 kg m2, who don’t practice exercise regularly.
  • Subjects who experience body pain after vyayama and with Defense and Veterans pain rating scale (DVPRS)equal to or greater than
  • Subjects aged between 25 to 50 years irrespective of the gender occupation and socio-economic status.
  • 4.Subjects who are fit for udvartana.

排除标准

  • Subjects who are on regular analgesic medication.
  • Subjects with impaired mobility.
  • Subjects who are unfit for Vyayama.
  • Subjects who can’t follow the instructions given.

结局指标

主要结局

1. To study the effectiveness of udvartana in preventing pain given before vyayama on subjects with pain induced due to vyayama.

时间窗: 5 DAYS

2. To study the effectiveness of udvartana in alleviating pain given after vyayama on subjects with pain induced due to vyayama.

时间窗: 5 DAYS

3. To compare the effectiveness of udvartana given pre and post vyayama on subjects with pain induced due to vyayama in order to ascertain the best sequence.

时间窗: 5 DAYS

次要结局

  • 1. BMI before and after the intervension.

研究者

发起方
Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Adithi B

Sri Dharmasthala Manjunatheshwara College of Ayurveda andHospital

研究点 (1)

Loading locations...

相似试验