Can a quick mindfulness session ease stress for COVID-19 frontline workers?
NCT ID NCT04555005
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested a brief, on-site mindfulness program for 1,000 frontline healthcare workers in a Madrid hospital during the COVID-19 outbreak. The goal was to see if it could help reduce stress right away. Participants rated how helpful it was on a scale of 0 to 10. The study was completed and aimed to provide a simple tool for hospitals to support staff during crises.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mindfulness-based intervention
- What this could lead to
- If successful, this could show that a short, on-site mindfulness program helps healthcare workers manage stress during a crisis.
- What could go wrong
- This was a small, single-arm study with no comparison group, so results may be due to other factors. It also focused on immediate stress relief, not long-term effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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1,000 people
The number who actually took part.
- Started
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Mar 2020
- Finished
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Apr 2020
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All frontline healthcare workers present in the ward at the time of intervention Exclusion Criteria: * Extreme adverse events
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
La Paz University Hospital
Madrid, Madrid, 28046, Spain
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Other studies related to the condition(s) this trial covers.
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