Happy Nurse Project: Lifestyle Interventions to Maintain Healthy Mental State in Hospital Nurses (HNP)
Depressive Disorder, Anxiety Disorders

About this trial
This is an interventional prevention trial for Depressive Disorder
Eligibility Criteria
Inclusion Criteria:
- Work for inpatient wards in among four general hospitals in Tama region, Japan, including: National Center of Neurology and Psychiatry Hospital, National Disaster Medical Center, Tokyo Metropolitan Tama Medical Center, and Tama-Hokubu Medical Center
- Nurses without administration work
- Give written consent in the participation of the study
Exclusion Criteria:
- Have plans to take sick leave, leave for other reasons or retirement within 26 weeks from the entry to the study
- Take structured psychotherapy (e.g. cognitive behavioral therapy, interpersonal therapy, and brief psychodynamic therapy) at the entry
- See a physician regularly in order to treat any mood or anxiety disorders primarily at the entry
- Take antidepressants, mood stabilizers, anticonvulsants or antipsychotics at the entry
- Have taken nutrient supplement including omega-3 fatty acids for 4 or more weeks within 52 weeks from the entry
- Clinically depressed, based on the total score of 11 or more on the Hospital Anxiety and Depression Scale - Depression Subscale and the total score of 15 or more on the Primary Health Care Questionnaire
- Consume 4 times or more of fish as the main course of meal per week
- Take anticoagulant drugs at the entry or have previous history of stroke or myocardial infarction
- Judged ineligible by research coordinator due to any reason
Sites / Locations
- National Center of Neurology and Psychiatry
- Kyoto University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Active Comparator
Active Comparator
Active Comparator
Stress management plus omega-3
Stress management plus placebo
Psychoeducation leaflet plus omega-3
Psychoeducation leaflet plus placebo
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.