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Clinical Trials/NCT05515172
NCT05515172
Completed
Not Applicable

Resilience Intervention in Times of Crisis for Health Professionals During the COVID-19 Contingency

Universidad de Monterrey1 site in 1 country371 target enrollmentApril 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mental Health Wellness 1
Sponsor
Universidad de Monterrey
Enrollment
371
Locations
1
Primary Endpoint
Change from Baseline to 6 months follow-up of Negative Emotions
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

In the fight against the coronavirus (COVID-19) pandemic, health personnel, especially nursing staff, have been facing enormous pressure, including a high risk of infection and inadequate protection against contamination, overwork, frustration, discrimination, isolation, lack of contact with their families and exhaustion. Therefore, the World Health Organization (WHO) has requested particular interventions to promote emotional well-being in health workers exposed to COVID-19, which must be implemented immediately, especially those aimed at women and nursing staff. . Psychological support services, including counseling or intervention via phone, internet, and apps, have been widely deployed by local and national mental health institutions in response to the COVID-19 outbreak. Complementing these efforts, the present study seeks, through mind-body medicine strategies, to promote resilience among nurses exposed to COVID-19 in critical phases. A multidisciplinary team of expert volunteers designed the intervention in different mind-body medicine techniques (for example, medicine, psychology, thanatology, meditation, health, and wellness coaches, certified Qi Gong, and yoga instructors) and is made up of 3 components main: "micropractices," cohesion and support groups, which will be implemented for 12 weeks in health personnel. This intervention responds to the international call to promote health personnel's physical and emotional health during the COVID-19 pandemic, offering an opportunity to accompany them during this time and mitigate the effects on health in the short and long term.

Registry
clinicaltrials.gov
Start Date
April 1, 2020
End Date
April 1, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent

Exclusion Criteria

  • Lack of signature in the informed consent

Outcomes

Primary Outcomes

Change from Baseline to 6 months follow-up of Negative Emotions

Time Frame: At baseline, and 6 months follow-up

Negative Emotions will be measured using the PERMA Profiler which evaluates positive emotions, engagement, relationships, meaning, accomplishments, perception of health, and negative emotions.

Change from Baseline to 6 months follow-up of Perception of Health

Time Frame: At baseline, and 6 months follow-up

Perception of Health will be measured using the PERMA Profiler which evaluates positive emotions, engagement, relationships, meaning, accomplishments, perception of health, and negative emotions.

Change from Baseline to 6 months follow-up of Resilience

Time Frame: At baseline and 6 months follow-up

Resilience will be measured using the brief resilience scale

Change from Baseline to 6 months follow-up of Subjective Well-being

Time Frame: At baseline, and 6 months follow-up

Subjective Well-Being will be measured using the PERMA Profiler which evaluates positive emotions, engagement, relationships, meaning, accomplishments, perception of health, and negative emotions.

Change from Baseline to 6 months follow-up of Stress

Time Frame: At baseline and 6 months follow-up

Stress will be measured using the perceived stress scale.

Change from Baseline to 6 months follow-up of mindfulness

Time Frame: At baseline and 6 months follow-up

Resilience will be measured using the mindfulness-awareness attention scale

Change from Baseline to 6 months follow-up of burnout

Time Frame: At baseline and 6 months follow-up

Burnout will be measured using the Burnout Clinical Subtypes Questionnaire

Study Sites (1)

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