- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04387643
Protecting Health Care Workers During the COVID-19 Outbreak
May 13, 2020 updated by: Aarogyam UK
Protecting Health Care Workers During the COVID-19 Outbreak:Qualitative Study of AYUSH Initiative
Preparing to deal with Covid-19 outbreak in Rajasthan, India, health care workers were given Ayurvedic Kadha (combination of ayurvedic herbal extracts) starting from the end of February 2020.
Then, majority of these health care workers were put on front line managing screening, monitoring, quarantine and treating Covid 19 patients.
This real-life study aimed to determine the experience of health care workers who had Ayurveda kadha before starting as front-line workers.
Study Overview
Study Type
Observational
Enrollment (Actual)
52
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Rajasthan
-
Jaipur, Rajasthan, India
- Samta Ayurveda Prakoshtha
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Health care workers at front line of Covid-19 screening, treatment and management
Description
Inclusion Criteria:
- Health care workers posted in Covid-19 duties at front line
- Health workers who had Ayurveda herbs combination over for at least 10-days
Exclusion Criteria:
- No willing to consent
- inability to participate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical Health
Time Frame: From baseline to 30-days
|
Self-reported health issues
|
From baseline to 30-days
|
|
Psychological Health
Time Frame: From baseline to 30-days
|
Self-reported psychological issues
|
From baseline to 30-days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Coping with distress
Time Frame: From baseline to 30-days
|
Self-reported coping with high demanding work in Covid-19 duties
|
From baseline to 30-days
|
|
Self-Help
Time Frame: From baseline to 30-days
|
Self reported self-help measures used
|
From baseline to 30-days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Jaydeep Joshi, Aarogyam UK
- Study Chair: Neha Sharma, British Ayurvedic Medical Council (UK)
- Study Director: Parashar Sharma, Samta Ayurveda Prakoshtha, India
- Principal Investigator: Sahil Singhal, Samta Ayurveda Prakoshtha, India
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2020
Primary Completion (Actual)
April 2, 2020
Study Completion (Actual)
April 2, 2020
Study Registration Dates
First Submitted
May 13, 2020
First Submitted That Met QC Criteria
May 13, 2020
First Posted (Actual)
May 14, 2020
Study Record Updates
Last Update Posted (Actual)
May 14, 2020
Last Update Submitted That Met QC Criteria
May 13, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AU/SA/01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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