The Selah study protocol of three interventions to manage stress among clergy: a preference-based randomized waitlist control trial.
Study Goal
The researchers aimed to compare the effectiveness of mindfulness-based stress reduction, Daily Examen, and stress inoculation training in reducing stress symptoms among clergy.
Results Summary
The study measured self-reported stress symptoms and heart rate at 12 weeks, with secondary outcomes including anxiety symptoms, but specific results for mindfulness were not detailed in the abstract.
Population
United Methodist clergy in North Carolina.
Effective Dosage
Not specified.
Duration
12 weeks (primary outcome measurement).
Interactions
None mentioned.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
mindfulness-based stress reduction | decrease | self-reported symptoms of stress | United Methodist clergy in North Carolina | - | compared to waitlist control | #1 |
mindfulness-based stress reduction | decrease | heart rate | United Methodist clergy in North Carolina | - | compared to waitlist control | #2 |
mindfulness-based stress reduction | decrease | symptoms of anxiety | United Methodist clergy in North Carolina | - | compared to waitlist control | #3 |
Daily Examen | decrease | self-reported symptoms of stress | United Methodist clergy in North Carolina | - | compared to waitlist control | #4 |
Daily Examen | decrease | heart rate | United Methodist clergy in North Carolina | - | compared to waitlist control | #5 |
Daily Examen | decrease | symptoms of anxiety | United Methodist clergy in North Carolina | - | compared to waitlist control | #6 |
stress inoculation training | decrease | self-reported symptoms of stress | United Methodist clergy in North Carolina | - | compared to waitlist control | #7 |
stress inoculation training | decrease | heart rate | United Methodist clergy in North Carolina | - | compared to waitlist control | #8 |
stress inoculation training | decrease | symptoms of anxiety | United Methodist clergy in North Carolina | - | compared to waitlist control | #9 |
INTRODUCTION: Like many helping professionals in emotional labor occupations, clergy experience high rates of mental and physical comorbidities. Regular stress management practices may reduce stress-related symptoms and morbidity, but more research is needed into what practices can be reliably included in busy lifestyles and practiced at a high enough level to meaningfully reduce stress symptoms. METHODS AND ANALYSIS: The overall design is a preference-based randomized waitlist control trial. United Methodist clergy in North Carolina will be eligible to participate. The intervention and waitlist control groups will be recruited by email. The interventions offered are specifically targeted to clergy preference and include mindfulness-based stress reduction, Daily Examen, and stress inoculation training. Surveys will be conducted at 0, 12, and 24 weeks with heart rate data collected at 0 and 12 weeks. The primary outcomes for this study are self-reported symptoms of stress and heart rate at week 12 for each intervention compared to waitlist control; the secondary outcome is symptoms of anxiety comparing each intervention vs waitlist control. ETHICS AND DISSEMINATION: Ethical approval was obtained from the Duke University Campus IRB (2019-0238). The results will be made available to researchers, funders, and members of the clergy community. STRENGTHS AND LIMITATIONS OF THIS STUDY: While evidence-based stress reduction practices such as mindfulness-based stress reduction (MBSR) exist, a wider variety of practices should be tested to appeal to different individuals. Clergy in particular may prefer, and consequently enact, spiritual practices like the Daily Examen, and individuals such as clergy who spend most of their time thinking and feeling may prefer experiential-based practices like stress inoculation training. If efficacious, the Daily Examen and stress inoculation training practices have high feasibility in that they require few minutes per day. This study is limited by the inclusion of Christian clergy of only one denomination. TRIAL REGISTRATION: ClinicalTrials.gov NCT04625777 . November 12, 2020.