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