Buckeye Pause Bundle | NCT07720297

NCT07720297

Overview

NCT ID: NCT07720297
Lead Sponsor: Ohio State UniversityOTHER
Official Title: The Buckeye Pause Bundle: Augmenting State of Mind and Body as the Ultimate Personal Protective Equipment (PPE)
Brief Summary: Mind-body resilience is particularly important in workplaces where there are frequent exposures to primary or secondary emotional and/or physical trauma. A 2020 report from the U.S. Bureau of Labor Statistics highlighted health workers as among the largest service industries in the state of Ohio with the most amount of missed work days due to injury or illness. The purpose of this study is to develop and establish proof-of-concept of the "Buckeye Pause Bundle," a proactive workplace facilitation of mind-body resilience protective and recovery activities that includes an evidence-based mindfulness-based intervention, a wearable health device that offers user prompts and reminders based on physiological data, and worksite respite pods to support brief mindfulness practices during the workday. The target market segment for this proof-of-concept testing is healthcare providers working in acute care hospital settings. It is anticipated that end prototypes and deliverables will be very transferable to other high-stress work environments.

Status and Timeline

Status: Completed
Last Update Posted: Jul 22, 2026Actual
Start Date: Aug 12, 2022Actual
Primary Completion Date: Jun 1, 2023Actual
Completion Date

Participation Criteria

Ages Eligible for Study: Adult (18-64)Older Adult (65+)
Sexes Eligible for Study: All
Accepts Healthy Volunteers?: Yes
Eligibility Criteria: Inclusion Criteria:

18 years or older

Actively employed as a healthcare professional/healthcare employee at one of four associated hospitals in Ohio

Ability to read and speak English.

Access to a personal smartphone or computer and willingness to download study applications.

WiFi access in order to enable access to study related materials, i.e. questionnaires, study instructions, etc.

Exclusion Criteria:

1. Previously participation/completion of the Mindfulness in Motion program.

Study Plan

Study Type: Interventional
Phase: Not Applicable
Enrollment: 220Actual
Primary Purpose: Supportive Care
Allocation: Non-Randomized
Interventional Model: Parallel Assignment
Masking: None (Open Label)

Contacts and Locations

Central Contacts: No data available
Locations: Ohio State University Wexner Medical Center

Similar Studies

Participant Group/Arms

Augmented Mindfulness-based InterventionExperimental

Mindfulness in Motion (8-week mindfulness-based intervention) that includes access to companion website or smartphone app for supplementary information to support individual practice outside of in-person weekly sessions plus use of Oura ring wearable plus access to worksite respite spaces

Behavioral: Augmented Mindfulness-based Intervention

Mindfulness-based interventionActive Comparator

Mindfulness in Motion (8-week mindfulness-based intervention) that includes access to companion website for supplementary information to support individual practice outside of in-person weekly sessions.

Behavioral: Mindfulness-based intervention