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

Status

Completed

Conditions

Intervention / Treatment

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

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

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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