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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04555005
Other study ID # Mind-COVID-19
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 10, 2020
Est. completion date April 26, 2020

Study information

Verified date March 2020
Source Instituto de Investigación Hospital Universitario La Paz
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The COVID-19 outbreak is having an impact on the well-being of healthcare workers. Previous reports on pandemics show that such an impact may last beyond the time of the outbreak. Mindfulness-based interventions help healthcare professionals to reduce stress and may foster resilience and recovery, although they have never been tested in a context such as the current one. This single-arm trial explores the acceptability, safety and usefulness of an on-site, brief Mindfulness-based intervention to reduce stress for front line health workers during a crisis.


Recruitment information / eligibility

Status Completed
Enrollment 1000
Est. completion date April 26, 2020
Est. primary completion date April 26, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- All frontline healthcare workers present in the ward at the time of intervention

Exclusion Criteria:

- Extreme adverse events

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mindfulness based intervention
Mindfulness based intervention for frontline healthcare workers during COVID-19 outbreak

Locations

Country Name City State
Spain La Paz University Hospital Madrid

Sponsors (2)

Lead Sponsor Collaborator
Instituto de Investigación Hospital Universitario La Paz Hospital Universitario La Paz

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived helpfulness to reduce current stress The outcome was measured by a 10-point visual analogue scale developed for this study, where 0 was "it did not help me at all" and 10 was "it helped me a lot". through study completion, up to three days
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