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临床试验/CTRI/2025/02/081079
CTRI/2025/02/081079尚未招募2/3 期

Exploring the interplay between sadvritta and its role in the management of vishaada (Depression):A multidimensional analysis

Bornali Biswas1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年2月25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
30
试验地点
1
主要终点
The study will be done to observe the effects of sadvritta on the patients diagnosed with depression having mild to moderate symptoms by councelling them . Patients will be diagnosed on basis of hamilton depression rating scale . The scores will be recorded before and after treatment which will further decide the effect of treatment on the patient.

研究概览

简要总结

The study will be done to find out the applicability of sadvritta in management of vishaada (depression) on a sample size of 30 patients of OPD and IPD of Government Ayurvedic College and Hospital Guwahati Assam in the age group of 18 to 70 years irrespective of gender for a period of 60 days . The management will be done by councelling the patients about sadvritta and its application in lifestyle modifications who are suffering from depression . The scores before and after treatment will be recorded as per hamilton depression rating scale .

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients having symptoms of depression as per DSM V criteria will be selected for the present research work irrespective of gender.

排除标准

  • Patients below 18 years of age and above 70 years will be excluded.Severe psychiatric problems,severe cognitive problems, bedridden patients, patients using oral antidepressants will be excluded during the study.

结局指标

主要结局

The study will be done to observe the effects of sadvritta on the patients diagnosed with depression having mild to moderate symptoms by councelling them . Patients will be diagnosed on basis of hamilton depression rating scale . The scores will be recorded before and after treatment which will further decide the effect of treatment on the patient.

时间窗: The patient will be under the trial for a period of 60 days

次要结局

  • The patients will undergo the treatment through four subsequent follow up after every 15 days till completion of sixty days .(The first follow up will be after 15 days after first visit , the next on 30 th day, then 45th day and lastly 60th day.)

研究者

发起方
Bornali Biswas
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Bornali Biswas

Government Ayurvedic College and Hospital Guwahati Assam

研究点 (1)

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