Compassion Fatigue, Healthcare Providers, Healthcare Workers, Job Stress, Psychological Trauma, Workplace Stress
Conditions
Keywords
COVID-19, Coronavirus, Healthcare staff, Work stress, insomnia, anxiety, depression, resilience, mind-body intervention
Brief summary
This study will examine the feasibility of conducting an online Randomized Controlled Trial (RCT) in frontline hospital and long term care healthcare staff in managing COVID-19 patients in London, ON. The study will randomize participants to Sudarshan Kriya Yoga (SKY) or a Health Enhancement Program (HEP).
Detailed description
The COVID-19 pandemic continues to escalate as a global health threat, leading to devastating impacts on the healthcare system. Frontline healthcare workers are dealing with increased demands and fears for their own, as well as their family's safety. Adding to the stress is the limited ability to maintain social connectedness as physical distancing measures are in place. The investigators plan to conduct an open-label feasibility randomized controlled trial (RCT), comparing an online breath based yogic intervention called Sudarshan Kriya Yoga (SKY) (n=30) versus an online control mind-body intervention called the Health Enhancement Program (HEP) (n=30) in 60 hospital and long term care frontline staff that are managing COVID-19 patients. Participants will be blinded to the treatment hypothesis while data analyst will be blinded to treatment allocation. Both SKY and HEP will be taught online in two phases in the first week followed by weekly reinforcement sessions for the following 4 weeks. Feasibility measures will be assessed as well as self-rated measures of insomnia, anxiety, depression, and resilience. The investigators expect that it will be feasible to conduct an online RCT of two mind-body interventions, SKY and HEP, in staff managing the COVID-19 pandemic, and that the investigators will be able to remotely monitor safety and efficacy of these interventions.
Interventions
The SKY program is a standardized, easy to learn sequential breathing yoga consisting of regulated breathing techniques followed by a timed rhythmic breathing practice. Participants will learn various exercises including rhythmic breathing, gentle yoga, and guided meditation.
HEP is a structured group program designed to help participants with information and instruction how to lead a healthier life. Participants will be provided psychoeducation and support regarding healthy active living using techniques like music therapy, diet control, exercise, and monitoring these via journaling.
Sponsors
Art of Living Foundation
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
Participants will be blinded to the treatment hypothesis while the data analyst will be blinded to treatment allocation.
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
1. Participants will be frontline hospital or long-term care home staff involved in the management of COVID-19 patients in Canada or The United States of America. 2. Participants will be aged 18 to 70. 3. Participants will be willing and able to attend, via WebEx software, the introductory phase of SKY or HEP, as well as at least two of the four weekly follow-up sessions 4. Have sufficient hearing to follow verbal instructions. 5. Have an adequate understanding of English. 6. Able to sit without physical discomfort for 60 minutes. 7. Not pregnant and willing to remain not pregnant for the duration of the study.
Exclusion criteria
1. Inability to independently provide informed consent. 2. Current suicidality as assessed by the suicide item of the Patient Health Questionnaire-9 scale. 3. History of bipolar disorder. 4. History of chronic PTSD. 5. History of schizophrenia or schizoaffective disorder. 6. Currently practice any type of formal meditation, mindfulness, or breathing techniques regularly (greater than 3 times per week). 7. History of complex PTSD.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Unexpected costs | 1 year | The total of unexpected costs will be calculated as a feasibility measure. |
| Rate of participant recruitment | 1 year | The number of participants recruited per month will be calculated as a feasibility measure. |
| Rate of retention | 1 year | The retention rate of participants will be calculated as a feasibility measure. |
| Completeness of data entry | 1 year | The completeness of study assessments will be assessed as a feasibility measure by calculating the missing percentage of data in case report forms. |
| Cost of interventions | 1 year | The cost of both study interventions will be calculated to assess the total study cost for interventions and the cost per participant. This information will be used as a feasibility measure. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Generalized Anxiety Disorder 7-item scale | Change from Week 0 to week 3 and to week 5 | The Generalized Anxiety Disorder 7-item scale (each scored 0-3) is a self-rated measure of anxiety and has been validated for the diagnosis of Generalized Anxiety Disorder in the adult population. Scores range from 0 to 21. Higher scores indicate greater anxiety symptoms (5-9, mild anxiety; 10-14, moderate anxiety; 15-21 severe anxiety). |
| Change in Patient Health Questionnaire 9 | Change from Week 0 to week 3 and to week 5 | The Patient Health Questionnaire (PHQ-9) is a 9-item, self-rated measure of depression which has been validated for screening a major depressive episode in adults. Total scores indicate various levels of depression: 0-4, no depression; 5-9, mild depression; 10-14, moderate depression; 15-19, moderately severe depression; 20-27, severe depression. |
| Change in Connor-Davidson Resilience Scale | Change from Week 0 to week 3 and to week 5 | The Connor-Davidson Resilience Scale (CD-RISC) is a brief self-rated assessment tool that comprises of 10 items, each rated on a 5-point Likert scale (0 = not true at all to 4 = true nearly all the time). Higher scores reflect greater resilience, which is a measure of one's ability to cope with stress. The scale demonstrated strong reliability and validity and has been studied in a variety of populations including medical personnel, nurses, social workers and physicians). |
| Change in Athens Insomnia Scale | Change from Week 0 to week 3 and to week 5 | The Athens Insomnia Scale will be used to assess insomnia. This scale is an 8-item, self-rated measure of the extent of sleep difficulties over the last 30 days with each item representing a different aspect of sleep (e.g. Overall Quality of Sleep). Ratings are from 0 to 4, with 0 being no difficulty with the item and 4 being the most difficulty with the item. Higher overall scores on this scale indicate higher difficulties with sleep. |
Countries
Canada
Outcome results
None listed