NCT06925503

Brief Summary

Mindfulness in Motion (MIM) is an eight-week evidenced based program designed specifically to help participants learn practical stress reduction, burnout and resiliency building techniques. Content includes didactic instruction, community-building group discussion, mindfulness practices, and gentle yoga. Weekly themes include Willingness to Daily Practice, Mindful Sleep, Vision of Self, Supported by the Breath, Mindful Eating and Yoga, Movement Through Balance, Awareness of Sensation, Clarity and Release, and Staying Grounded and Moving Forward. An Ohio State University endorsed, ADA compliant companion smartphone app reinforces weekly content and offers a variety of individual mind-body and mediations practices. The evidence-based MIM content has been tailored to meet the physical, mental, and emotional needs of student Dance majors at The Ohio State University and integrated into the Dance 2802 course content as Mind-Body Conditioning for second year students. Over the course of the second year student's fall semester, this study will evaluate the effectiveness of this integrated course content on students' perceived stress, burnout, resilience, musculoskeletal injury and discomfort, and weekly respiratory rates. After the semester long course is completed, the students will also assess how well the Mind-Body Conditioning course content was integrated into the required first year seminar for University Dance majors.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 6, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 13, 2025

Completed
5 months until next milestone

Study Start

First participant enrolled

September 10, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 19, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
Last Updated

January 2, 2026

Status Verified

September 1, 2025

Enrollment Period

3 months

First QC Date

April 6, 2025

Last Update Submit

December 30, 2025

Conditions

Outcome Measures

Primary Outcomes (5)

  • Perceived Stress

    Perceived Stress Scale-10 (PSS-10). A 10-item self-report measure of perceived stress. It is a measure of the degree to which situations in one's life are appraised as stressful over the past month. The 4-point Likert Scale includes responses of 0 (never), 1 (almost never), 2 (sometimes), 3 (fairly often), and 4 (very often). Individual scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress.

    Baseline and on completion of the 8-week intervention

  • Maslach Burnout Inventory-Students - MBI-GS (S)

    The MBI-GS (S) is a self-report assessment of perceptions of burnout specific to University students. The 16-items describe students' feelings related to their experiences in the academic setting and encompasses how they view their studies and reactions to their academic work. Three sub scales measure exhaustion, cynicism, and professional efficacy. The Likert Scale responses include 0 (never), 1 (a few times a year or less), 2 (once a month or less), 3 (a few times a month), 4 (once a week), 5 (a few times a week), and 6 (every day). The sub scale score for exhaustion can range from 0 to 30 with higher scores indicating higher levels of exhaustion. The sub scale score for cynicism can range from 0 to 30 with higher scores indicating higher levels of cynicism. The sub scale score for professional efficacy can range from 0 to 36 with higher scores indicating increased professional efficacy.

    Baseline and on the completion of the 8-week intervention

  • Resilience

    The Connor-Davidson Resilience Scale-10 (CD-RISC-10) is a 10 item self-report assessment of a person's ability to bounce back after adversity. A 5-point Likert Scale for each statement ranges from 0 (not true at all), 1 (rarely true), 2 (sometimes true), 3 (often true), 4 (true nearly all of the time). A respondent's total score can range from 0 to 40 with higher scores indicating higher resilience.

    Baseline and on completion of the 8-week intervention

  • Respiratory Rate

    A self-measured count of inhalations (respiratory rate) taken over a 30-second time period. The participant will place their right hand over their left chest and count inhalations for a 30-second time period before and after they participate in the Mind-Body Conditioning course at each 8-week session.

    The 30-second count of inhalations will be completed by the participant before and after participating in each weekly Mind-Body Conditioning course session over eight weeks.

  • Modified Nordic Questionnaire

    The Modified Nordic Questionnaire (mNMQ) is a 14-item scale measuring musculoskeletal discomfort and injury. Question 1 asks the participant to state if they have experienced pain, discomfort, burning, numbness, tingling or other trouble over the past 30 days in their neck, shoulder, elbow/forearm, wrist/hand, upper and lower back, and legs/feet. Questions 2 - 10 asks about the intensity and length of the the pain, discomfort, etc, in any of the body areas noted in Question 1, as well as if the issues have caused issues with normal activities, to see a health care provider, lost time from work/school. Question 11 requests information related to any musculoskeletal or traumatic injuries diagnosed by a health care provider. Questions 12 and 13 request information on headaches experienced by participants and question 14 asks about other health issues including arthritis, thyroid problems, diabetes, lupus, and other autoimmune disorders.

    Baseline and on completion of the 8-week intervention

Secondary Outcomes (1)

  • Feasibility of Intervention Measure

    Participants will complete after the completion of the 8-week intervention.

Study Arms (2)

Second Year Dance majors

EXPERIMENTAL

Second year Dance majors at The Ohio State University who are enrolled in the required Dance 2802 Seminar/Mind-Body Conditioning course

Behavioral: Mind-Body Conditioning Course

Third Year Dance majors

NO INTERVENTION

The Third Year Dance majors completed Dance 2802 the previous year and did not receive the Mind-Body Conditioning course

Interventions

Evidence-based mindfulness intervention curated to the physical and emotional needs of University Dance students

Second Year Dance majors

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • years of age or older
  • Ability to understand and read English
  • Second year OSU Dance majors enrolled in Dance 2802 for Fall 2025 semester
  • Third year OSU Dance majors who completed Dance 2802 during the 2024-2025 academic year.
  • Access to personal smartphone, either iOS or Android, with sufficient memory to install the Mindfulness in Motion smartphone app, and WiFi (OSU eduroam while in class or on campus and LTE or personal WiFi off campus)

You may not qualify if:

  • OSU student with a minor in Dance.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Ohio State University

Columbus, Ohio, 43210, United States

Location

MeSH Terms

Conditions

Burnout, PsychologicalMusculoskeletal Abnormalities

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehaviorMusculoskeletal DiseasesCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Director of Research

Study Record Dates

First Submitted

April 6, 2025

First Posted

April 13, 2025

Study Start

September 10, 2025

Primary Completion

December 19, 2025

Study Completion

May 1, 2026

Last Updated

January 2, 2026

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will share

IPD that will be shared will include de-identified descriptive data for both the intervention and control groups, including gender, educational level, and mean age. Feasibility of integrating the intervention into the required course content by the intervention group will also be included. Differences in mean scores between intervention and control groups for perceived stress, burnout, resilience, and respiratory rates (pre- and post-intervention) will be shared. Descriptive data for any differences in the modified Nordic Questionnare pre- and post-intervention will be shared.

Shared Documents
ICF, CSR, ANALYTIC CODE
Time Frame
7-30-26 to indefinitely
Access Criteria
De-identified and curated demographic, statistical data, study overview, study consent will be accessible to academic researchers and educators through a data accessibility link once the data to a repository is finalized.

Locations