NCT04716647已完成不适用
A Community-Based Participatory Research to Assess the Feasibility of Ayurveda Intervention in Patients With Mild-to-Moderate COVID-19
Aarogyam UK1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2020年10月9日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 28
- 试验地点
- 1
- 主要终点
- Time to clinical recovery
研究概览
简要总结
Innovative strategies are required to manage COVID-19 in the communities. Back to Roots community based project was a collaborative, pilot intervention program in British Asian community to assess the efficacy and safety of Ayurveda intervention in relieving symptoms of mild-to-moderate COVID-19.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •With SARS-CoV-2 infection confirmed through reverse transcription followed by polymerase chain reaction (RT- PCR),
- •With mild or moderate manifestations of COVID-19
- •Willing to participate, and consent by signing the informed consent and
- •not involved in another clinical trial during the study
排除标准
- •Patients suffering from severe COVID-19 Disease as per World Health Organisation criteria (REF)
- •Any of the known COVID-19 complications and emergency procedures which may require shift/admission in hospital for oxygen support or intensive care unit
- •Patients with ongoing immunosuppressive therapy for any reasons
- •Active cancer diagnosis, on palliative treatment or requiring current therapy with antimetabolic agents, immunotherapy or radiotherapy.
- •Pregnancy and lactation
- •Ayurveda practitioner decision that involvement in the study is not in the patient's best interest
结局指标
主要结局
Time to clinical recovery
时间窗: Up to 14-days
To evaluate the therapeutic efficacy, mean days for clinical recovery were recorded from AiM Covid Application
Proportion of patient with negative conversion in nasopharyngeal swab
时间窗: Up to 14 days
To evaluate the therapeutic efficacy, promotion of patients were recorded through AiM Covid application
次要结局
- Clinical Outcome(Up to 14-days)
研究者
研究点 (1)
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