The Effectiveness of RPSG Intervention for Nurses During the COVID-19
COVID-19 Acute Respiratory Distress Syndrome
About this trial
This is an interventional supportive care trial for COVID-19 Acute Respiratory Distress Syndrome focused on measuring psychological support group, nurse, COVID-19, quality of life
Eligibility Criteria
Inclusion Criteria:
- The nurses have to above 20 years old.
- The nurses who work in evacuation acute wards.
Exclusion Criteria:
- The nurses who have any mental illness.
Sites / Locations
- National Taiwan University Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Remote Psychological Support Group
Mindfulness through audio and video
The study will invite nurses through QR code on line, and assess their background, self-efficacy, fear of COVID-19, psychological distress, and quality of life by questionnaires first. Then four evacuation acute wards (A, B, C, and D) will be randomly allocated, and the two wards will be drawn out as experimental group ward. Each group will be followed for 2 months and their outcomes will be assessed at 3 time points: baseline (pre-RPSG) (T0), and 4 (T1), 8 (T2) weeks after-RPSG, T0-T2, respectively.
The study will invite nurses through QR code on line, and assess their background, self-efficacy, fear of COVID-19, psychological distress, and quality of life by questionnaires first. Then four evacuation acute wards (A, B, C, and D) will be randomly allocated, and the two wards will be drawn out as experimental group ward. Each group will be followed for 2 months and their outcomes will be assessed at 3 time points: baseline (pre-RPSG) (T0), and 4 (T1), 8 (T2) weeks after-RPSG, T0-T2, respectively.