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autonomous use condition for Stress
N/A
Waitlist Available
Led By Todd Hall, PhD
Research Sponsored by Biola University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 months
Awards & highlights
Study Summary
This trial tests if using a religious mobile app can reduce stress in people with high levels of stress. People will be randomly assigned to different conditions and measure results over 8 weeks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Perceived Stress Scale
Secondary outcome measures
Copenhagen Burnout Inventory--personal subscale
Daily Goal Progress Scale
Hospital Anxiety and Depression Scale
+5 moreTrial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: meditative prayer conditionExperimental Treatment1 Intervention
Participants will be given a free subscription to the Pray.com app and will be directed to listen to a meditation prayer five days per week.
Group II: autonomous use conditionExperimental Treatment1 Intervention
Participants will be given a free subscription to the Pray.com app and will be directed to use the app five days per week.
Group III: no intervention conditionActive Control1 Intervention
no intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
pray.com app (autonomous use)
2022
N/A
~320
pray.com app (meditative prayer condition)
2022
N/A
~320
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Who is running the clinical trial?
Biola UniversityLead Sponsor
1 Previous Clinical Trials
81 Total Patients Enrolled
Todd Hall, PhDPrincipal InvestigatorBiola University
1 Previous Clinical Trials
81 Total Patients Enrolled
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