Effectiveness Of Individualized Homeopathic Medicines in Improving The Social Quality of Life And Satisfaction in Depression Among Working Population- A Quasi Experimental Study
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 35
- 试验地点
- 1
- 主要终点
- Primary outcome will be measured by the difference between the score obtained in Q-LES-Q(sf)
研究概览
简要总结
This quasi experimental study evaluates the effectiveness of individualized homoeopathic medicines in improving the social quality of life and satisfaction in depression among the working population using Quality of Life Enjoyment and Satisfaction questionnaire Q-LES-Q (sf).Secondary objective include to find out the overall improvement in Depression among working population using Patient Health Questionnaire-9 (PHQ-9) scale and the reduction of work related burnout using Copenhagen Burnout Inventory (CBI) scale.Patients will be recruited from the Outpatient Department (OPD), Inpatient Department (IPD), and Peripheral Centres of the National Homoeopathic Research Institute in Mental Health (NHRIMH), Kottayam, based on ICD-11 criteria. Enrolment requires psychiatric confirmation, and informed consent will be obtained in English and Malayalam. Subjects will be assessed at baseline by using Patient Health Questionnaire (PHQ -9), Copenhagen Burnout Inventory scale (CBI) to get severity of the condition. The quality of life of the subjects will be assessed with Q-LES-Q-(sf) questionnaire. A detailed case history and mental status examination will be recorded, and individualized homoeopathic remedies will be prescribed based on repertorization via RADAR OPUS software and Homoeopathic Materia Medica. Acute exacerbations will be managed accordingly. Patients missing follow-ups for
three consecutive months will be considered dropouts and will receive standard OPD care but will be excluded from further study evaluation. The study aims to find out the effectiveness of Homoeopathic medicines in improving the social quality of life and satisfaction in Depression among working population.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Open Label
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Cases satisfying icd 11 diagnostic criteria Subjects of working population Subjects of both the sexes Score of Q-LES-Q(sf) greater than equal to 14 Score of PHQ9 greater than equal to 5.
排除标准
- •1.Depressive patients with severe suicidal ideation.
- •Mood disturbances when associated with schizophrenia spectrum disorder, Depressive episode in Bipolar affective disorder, other psychotic disorder.
- •Subjects who are pregnant or lactating.
- •Severe systemic illness.
- •Subjects who used psychotropic medicines in past 2weeks.
结局指标
主要结局
Primary outcome will be measured by the difference between the score obtained in Q-LES-Q(sf)
时间窗: Baseline at 3rd,6th,9th month and at the conclusion of the study (12th month)
questionnaire in the baseline and end of the treatment.
时间窗: Baseline at 3rd,6th,9th month and at the conclusion of the study (12th month)
次要结局
- Secondary outcome will be measured by the difference between the score obtained in Patients Health Questionnaire-9 scale(2.Copenhagen Burnout Inventory scale in the baseline and end of)