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Buckeye Pause Bundle

NCT07720297 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 220

Last updated 2026-07-22

No results posted yet for this study

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.

Conditions

  • Burnout
  • Work Engagement
  • Psychological Resilience
  • Work-Related Stress

Interventions

BEHAVIORAL

Augmented Mindfulness-based Intervention

8-week Mindfulness in Motion intervention that includes supplementary content through the Mindfulness in Motion website or smartphone app (to support individual practice outside of the in-person intervention) plus the use of an Oura ring to receive physiologic information, prompts, and text messages plus access to worksite respite spaces.

BEHAVIORAL

Mindfulness-based intervention

8-week Mindfulness in Motion program that includes access to website for supplementary information to support individual practice outside of in-person weekly sessions.

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • Maryanna Klatt, PhD · Ohio State University

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-08-12
Primary Completion
2023-06-01
Completion
2024-06-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07720297 on ClinicalTrials.gov