Mindfulness-Based Stress Management Program and Omega-3 Fatty Acids to Maintain Healthy Mental State in Hospital Nurses: Multi-Center Factorial-Design Randomized Controlled Trial Happy Nurse Project
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 80
- 试验地点
- 4
- 主要终点
- Blindly-rated depression and anxiety severity: Hospital Anxiety and Depression Scale (HADS)
研究概览
简要总结
The study is to explore the effectiveness of omega-3 fatty acids and mindfulness-based stress management program to maintain healthy mental state in hospital nurses. The participants will be junior nurses who work in inpatient wards and are not clinically depressed. The participants will be randomly allocated to four intervention arms: 1) Mindfulness-based stress management program plus omega-3 fatty acids pills ; 2) Mindfulness-based stress management program plus placebo pills; 3) Psychoeducation leaflet plus omega-3 fatty acids pills; and 4) Psychoeducation leaflet plus placebo pills. Thirty participants will be allocated to each arm. These interventions will terminate until three months from registration for each participant.
Information about depression and anxiety symptoms (primary outcome), insomnia, burnout, presenteeism, quality of life, sick leave, consultation about mental state of herself, and oxidative stress will be collected at 3 months, 6 months (primary time point) and 12 months from registration for each participant.
详细描述
The study is to explore the effectiveness of omega-3 fatty acids and mindfulness-based stress management program to maintain healthy mental state in hospital nurses. The participants will be junior nurses who work in inpatient wards at four general hospitals in Tama region in Tokyo, and are not clinically depressed based on the score of the Hospital Anxiety and Depression scale. The participants will be randomly allocated to four intervention arms: 1) Mindfulness-based stress management program plus omega-3 fatty acids pills; 2) Mindfulness-based stress management program plus placebo pills; 3) Psychoeducation leaflet plus omega-3 fatty acids pills; and 4) Psychoeducation leaflet plus placebo pills. Thirty participants will be allocated to each arm. These interventions will terminate until 3 months from registration for each participant. Stress management program will be conducted by senior nurses in four individual sessions within these three months. Psychoeducation leaflet will include information about screening of stress, sleep hygiene, relaxation, and a list of consultants about mental health.
Information about depression and anxiety symptoms (primary outcome), insomnia, burnout, presenteeism, quality of life, numbers of incident and accident at work, sick leave and consultation about mental state of herself, concentration of fatty acids in serum and oxidative stress will be collected at 3 months, 6 months (primary time point) and 12 months from registration for each participant. The primary outcome will be assessed by blind raters through telephone.
The outcomes will be compared between arms including stress management program and those without, and between arms including omega-3 fatty acids and those without, by using mixed model repeated measures model.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Factorial
- 主要目的
- Prevention
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 59 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •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
排除标准
- •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
研究组 & 干预措施
Stress management plus omega-3
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Mindfulness-based stress management program (Behavioral)
Stress management plus omega-3
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Omega-3 fatty acids pills (Dietary Supplement)
Stress management plus placebo
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Mindfulness-based stress management program (Behavioral)
Psychoeducation leaflet plus omega-3
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Psychoeducation leaflet (Behavioral)
Stress management plus placebo
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Placebo pills (Dietary Supplement)
Psychoeducation leaflet plus omega-3
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Omega-3 fatty acids pills (Dietary Supplement)
Psychoeducation leaflet plus placebo
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Psychoeducation leaflet (Behavioral)
Psychoeducation leaflet plus placebo
Thirty participants will be allocated to the arm. These interventions will terminate until 3 months from registration for each participant.
干预措施: Placebo pills (Dietary Supplement)
结局指标
主要结局
Blindly-rated depression and anxiety severity: Hospital Anxiety and Depression Scale (HADS)
时间窗: 26 weeks
The total score of the HADS (HADS-T) ranges from 0 to 42, with higher scores indicating more symptoms. The HADS has two sub scores, each ranging from 0 to 21: HADS-D (depression) and HADS-A (anxiety). The total score will be used as the severity of depression and anxiety symptoms in the present study.
次要结局
- Blindly-rated depression and anxiety severity: Hospital Anxiety and Depression Scale (HADS)(52 weeks)
- Depression severity: Personal Health Questionnaire-9 (PHQ-9)(52 weeks)
- Anxiety severity: Generalized Anxiety Disorder Assessment (GAD-7)(52 weeks)
- Burnout: Maslach Burnout Inventory (MBI)(52 weeks)
- Quality of Life: EuroQol (EQ-5D)(52 weeks)
- Major depressive episode: Primary Care Evaluation of Mental Disorders (PRIME-MD)(52 weeks)
- Insomnia severity: Insomnia Severity Index (ISI)(52 weeks)
- Presenteeism: World Health Organization Heath and Work Performance Questionnaire (HPQ)(52 weeks)
- Somatic symptoms: The Bradford Somatic Inventory (BSI)(52 weeks)
