CTRI/2024/03/064364招募中2 期
Efficacy of individualized homoeopathic medicines in reducing geriatric depression: A double blind, randomized, placebo-controlled trial - NI
D. N. De Homoeopathic Medical College and Hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •A. Elderly people with depression of not less than two weeks duration, with a minimum of two
- •typical and two common symptoms will be included in the study.
- •Typical symptoms:
- •o Depressed mood
- •o Loss of interest and enjoyment.
- •o Increased fatigability and diminished activity
- •Common symptoms:
- •o Reduced concentration and attention.
- •o Reduced self-esteem and self-confidence.
- •o Guilt feeling and unworthiness (mild type of episode)
- •o Bleak and pessimistic view of the future.
- •o Disturbed Sleep
- •o Diminished appetite
- •B. Age above 60 years
- •C. Mild and moderate depression [HDRS score - 8-13 mild, 14-18 moderate]
- •D. GDS-15 score more than 5
- •E. Participants having prior experience or knowledge of the treatment; e.g., primed to expect
- •‘homoeopathic aggravation’ and available treatment options for the disease conditions, intimated
- •through Patient Information Sheet.
排除标准
- •A. Mood disturbance when associated with bipolar affective disorder, schizophrenia,
- •schizophreniform disorder, schizoaffective disorder, or psychotic disorder.
- •B. Severe dementia (MoCA score less than 10)
- •C. Currently receiving any effective anti-depressant.
- •D. Active suicidal
- •E. Uncontrolled systemic disorders.
- •F. Undergoing homoeopathic treatment for any chronic disease within the last six months.
- •G. Vulnerable population- Unconscious, non-ambulatory, too sick for consultation, differently abled, terminally ill or critically ill patients, mentally incompetent people.
- •H. Self-reported immune-compromised state.
- •I. Patients with the habit of tobacco chewing and/or smoking, alcoholism, and/or
- •any other form(s) of substance abuse and/or dependence.
- •J. Simultaneous participation in any other clinical trials
- •K. Not Providing with written informed consent to participate voluntarily
研究者
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