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临床试验/CTRI/2024/08/072193
CTRI/2024/08/072193尚未招募3 期

Combined effect of vitamin D supplementation & Pulmonary Rehabilitation on asthma patients

SHARDA UNIVERSITY1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年8月20日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
200
试验地点
1
主要终点
Hospital Anxiety and Depression Scale.

研究概览

简要总结

This study is taken up to see the effect of vitamin D supplementation along with pulmonary rehabilitation on Asthma patients in Delhi NCR region. A sample of 200 patients, who will meet inclusion criteria will be participated to be apart of study100 subjects will be in controlled group 1 & 100 subjects will be ingroup 2 Consent form will be taken and pre- test measures will be done. Pulmonary Rehabilitation for 4 -6 weeks will be given which include general breathing exercises. The patients in PR group will attend a structured, comprehensive PR program for six weeks. This PR program will be institution based; therefore, the entire exercise protocol will be performed under the supervision of a qualified physiotherapist at the hospital .The PR program comprised of stretching of upper and lower extremity muscles, breathing exercises,self-management, and patient education. Breathing exercises will last for 30 minutes in each session and will performed two-to-thee times per week for six weeks. Diaphragmatic and pursedlip breathing will be performed

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
30.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • Patients who will be ready to provide informed consent Patients with mild & moderate Asthma Low vitamin D level as per American association of endocrinologists(less than30ng/ml) Receiving prescribed medication by physician.

排除标准

  • Smokers or patients suffering : hypothyroidism, liver or kidney diseases, cardiovascular disease, History of familial dyslipidemia, acute & chronic infections, fever, & malignancy Severe stage asthma patients Patients less than 30 & more than 55 years.

结局指标

主要结局

Hospital Anxiety and Depression Scale.

时间窗: 8 weeks

次要结局

  • SGRQ(8 weeks)

研究者

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

Prof.Dr Rahul Saxena

sharda university

研究点 (1)

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