Effect of an Online Self-help Psychological Intervention on Non-ICU Specialty Care During the COVID-19 Outbreak
SARS-CoV-2 Infection, Staff Attitude, Anxiety
About this trial
This is an interventional treatment trial for SARS-CoV-2 Infection
Eligibility Criteria
Inclusion Criteria: Age 18 years or older Non-ICU professional staff providing direct health care services to critically ill SARS-CoV-2 Omicron patients in the ICU Signing the informed consent form Exclusion Criteria: No reported acute suicidal tendencies No history of psychotic or dissociative symptoms Pregnancy or lactation Major family changes within the last 12 weeks( For e.g. death of immediate family member) Participated in other clinical trials
Sites / Locations
- The Second Affiliated Hospital of Zhejiang University anesthesiology departmentRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Intervention group
Control group
Daily members of the intervention group were thought to provide three different forms of daily sessions each day, averaging 10-20 minutes. These sessions included psycho-educational and cognitive-behavioral exercises, music therapy, sleep hygiene, stress relief methods. Weekly online lecture sessions presented by professional mental health therapists. In-depth interviews are conducted both before and after the experiment to explore the feasibility of the intervention
They will receive official mental health recommendations on how to cope mentally with the pandemic. These recommendations inform about the importance of a daily structure, social contact, acceptance of negative emotions and strengthening of positive emotions, and stimulus control to assimilate SARS-CoV-2 Omicron-related news. In-depth interviews are conducted both before and after the experiment to explore the feasibility of the intervention