跳至主要内容
临床试验/CTRI/2021/09/036110
CTRI/2021/09/036110尚未招募3 期

A Comparative Clinical Evaluation of Yoga Nidra and Preksha Meditation in the Management of Mixed Anxiety Depressive Disorder

UGC FELLOWSHIP AND CONTINGENCY1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年9月16日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
150
试验地点
1
主要终点
Reduction of the scores of

研究概览

简要总结

The research work is based on the patients suffering from MADD visiting to Sir Sundarlal Hospital, BHU, Varanasi under the supervision of Prof. J. S. Tripathi & Co- Supervision of 1. Prof. J.S. Yadav Department of Psychiatry IMS, BHU & 2. Prof. S. K. Dwivedi, Department of Sanskrit, Faculty of Arts, BHU. This is an interventional type of study in which two Yogic Interventions viz Yoga Nidra & Preksha Meditation has been selected. Study is being conducted on 150 patients randomly divided into 3 groups.

Diagnosed cases of MADD are  being registered from O.P.D. of Division of Manas Rog (Neuro – Psychiatry & Psychosomatic Medicine), Deptt. of Kayachikitsa, Sir Sundar Lal Hospital, I.M.S., B.H.U., Varanasi. DASS-42 Scale and WHO Quality of Life Bref Assessment Parameters are being used  for assessment of  anxiety and depression and quality of life of the patients of MADD.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • •1.Newly Diagnosed Patients fulfilling the diagnostic criteria of MADD according to DSM-
  • •Age range between 20-60 years belonging to either sex.
  • •Patients giving the informed consent.

排除标准

  • •1.Patients who have undergone treatment with MAO inhibitors or any other SSRI antidepressants
  • •Patients with prior history of seizures.
  • •3.Psychiatric diseases resembling clinical presentation of MADD like Major Depressive Disorder, Dysthymic Disorder, panic Disorder, or Generalized Anxiety Disorder.
  • •Patients having history of chronic illnesses such as Asthma, Tuberculosis and AIDS etc.

结局指标

主要结局

Reduction of the scores of

时间窗: 90 days

Improvement into the clinical signs and symptoms.

时间窗: 90 days

DASS. Improvement of the scores of WHO Quality of Life.

时间窗: 90 days

次要结局

  • Positive and promotive improvement in the mental health(90 days)

研究者

发起方
UGC FELLOWSHIP AND CONTINGENCY
申办方类型
Government funding agency

研究点 (1)

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