NCT05051969

Brief Summary

Stress, anxiety, and depression are common symptoms among public school teachers. Public school teachers are among the top professions reporting stress, anxiety, and depression. The causes are multifactorial and include work-related demands, challenges with students, limited resources, and compassion fatigue. Because of this, teachers are at risk of burnout and leaving or changing their profession. The COVID-19 pandemic has had a considerable impact on teachers due to disruptions in usual education delivery and ability to support students. Recent reports show poorer mental health and decreases in physical activity in teachers since the onset of the pandemic. Effective and implementable strategies are urgently needed to address poor mental health and to foster positive health characteristics in this population. Mindfulness programs decrease feelings of stress, anxiety, and emotional exhaustion. Additionally, mindfulness can improve self-compassion, which may be an important mediating factor in a teacher population. Prior work has shown an inverse relationship between self-compassion and burnout. Currently, there are few studies investigating whether building self-compassion can reduce burnout in public school teachers. The investigators will explore therelationship between participation in a Mindfulness-Based Stress Reduction (MBSR) course and changes in burnout, self-compassion, and other whole person health measures in an educator population. The overall objective of this open pilot study is to examine the feasibility and acceptability of an 8-week remote, group-based MBSR program delivered over Zoom for Metro Nashville Public Schools (MNPS) personnel reporting elevated stress, anxiety, and/or depressive symptoms. Our pilot study results will contribute to the evidence on MBSR in a public-school employee population and inform strategies to optimize implementation of our remote MBSR program within the Vanderbilt Health at MNPS system.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
37

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 12, 2021

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 21, 2021

Completed
9 months until next milestone

Study Start

First participant enrolled

July 1, 2022

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 5, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 5, 2023

Completed
Last Updated

February 8, 2023

Status Verified

February 1, 2023

Enrollment Period

6 months

First QC Date

September 12, 2021

Last Update Submit

February 7, 2023

Conditions

Keywords

BurnoutSelf-compassion

Outcome Measures

Primary Outcomes (4)

  • Feasibility - Recruitment

    Feasibility of recruitment will be assessed as the number of inviduals who are screened, eligible and enrolled in the study.

    Baseline

  • Feasibility- class attendance

    Percentage of participants that attend each scheduled session and who complete the program.

    Baseline to program completion (8 weeks)

  • Feasibility- enrollment retention

    Retention will be the number and proportion of indviduals who complete patient reported outcome data collection at 12-weeks.

    Baseline to 12 weeks after enrollment

  • Acceptability - Overall Helpfulness of the course

    Helpfulness of the course assessed by a one question survey with an 11-point Numeric Rating Scale ranging from 0 ("Not helpful") to 10 ("Most helpful"). Lower scores indicate less helpfulness.

    Baseline to 8 weeks

Secondary Outcomes (9)

  • Perceived stress as measured by a Perceived Stress Scale

    Baseline, 8 weeks and 12 weeks

  • Anxiety as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety short form

    Baseline, 8 weeks and 12 weeks

  • Depression as measured by the PROMIS Depression short form

    Baseline, 8 and 12 weeks after enrollment.

  • Mindfulness as measured by the Five Facet Mindfulness Questionnaire

    Baseline, 8 and 12 weeks after enrollment.

  • Physical health as measured by the 6-item Short Form Health Survey within the (SF-12)

    Baseline, 8 and 12 weeks after enrollment.

  • +4 more secondary outcomes

Study Arms (2)

8 Week Remote Mindfulness-Based Stress Reduction Program

EXPERIMENTAL

8 Week Remote MBSR Course for MNPS Employees.

Behavioral: Remote Mindfulness-Based Stress Reduction Program

8 week waitlist control

NO INTERVENTION

8 week waitlist control. They will complete the same assessments at baseline, 8 and 12 weeks

Interventions

Enrolled participants will participate in a remote-delivered (online with audio and video) Mindfulness-Based Stress Reduction (MBSR) program. MBSR is a well established behavioral health intervention consisting of 10-sessions lasting 2.5 hours, with one session lasting 7.5 hours in an all-day retreat format over a 2-month period.

8 Week Remote Mindfulness-Based Stress Reduction Program

Eligibility Criteria

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

You may qualify if:

  • Working certificated Metro Nashville Public Schools (MNPS) employees who self-report stress, anxiety, and/or depressive symptoms

You may not qualify if:

  • Unable to commit to the weekly MBSR schedule
  • Have taken the MBSR course previously
  • Participants who do not have reliable home internet

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vanderbilt University Medical Center

Nashville, Tennessee, 37203, United States

Location

MeSH Terms

Conditions

Burnout, PsychologicalAnxiety DisordersDepression

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehaviorMental Disorders

Study Officials

  • Martha E Shepherd, DO, MPH

    Vanderbilt University Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Clinical Medicine and Pediatrics

Study Record Dates

First Submitted

September 12, 2021

First Posted

September 21, 2021

Study Start

July 1, 2022

Primary Completion

January 5, 2023

Study Completion

January 5, 2023

Last Updated

February 8, 2023

Record last verified: 2023-02

Data Sharing

IPD Sharing
Will not share

Locations