- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06745934
Strengthening Health and Insight in New Educators (SHINE)
March 31, 2025 updated by: Summer Braun, University of Alabama, Tuscaloosa
Healthy Minds for Pre-Service Teachers
Teachers are at notable risk for depression and anxiety.
The present study tests an app-based mindfulness intervention for teachers in their final year of training with the goal of preventing the deterioration of their mental health during the transition into the classroom.
The project will strengthen the research environment at the University of Alabama and will involve undergraduate research assistants in each step of the research process.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Mental health concerns in teachers have escalated since the onset of the pandemic, and the deterioration of mental health can begin as early as the teacher training period.
Accessible and scalable programs that prepare teachers for the stress of the profession are urgently needed to prevent the deterioration of mental health and its attendant consequences.
The goal of this longitudinal project is to test the feasibility and acceptability, utility, and candidate mechanisms of an accessible, mobile health, mindfulness-based intervention, the Healthy Minds Program (HMP), to equip teachers in training ("pre-service teachers"; i.e., university students majoring in education) with skills necessary to maintain their mental health as they transition into the classroom.
The project addresses three specific aims.
Aim 1: a) Assess the feasibility and acceptability of the HMP for pre-service teachers and b) identify barriers and facilitators to program acceptability.
Aim 2: Determine the utility of the HMP for preventing depression and anxiety (main outcomes) and turnover intentions (secondary outcome).
Aim 3: Examine HMP effects on candidate mechanisms, and the effect of mechanisms on outcomes.
The results of this project will provide critical insight into the potential for the HMP to scale up for widespread use in pre-service teacher training programs.
Importantly, the project will provide a unique opportunity for undergraduate research at the University of Alabama, and will strengthen the research environment by involving undergraduate research assistants in each step of the research process.
Study Type
Interventional
Enrollment (Estimated)
140
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Summer S Braun, Ph.D.
- Phone Number: 2053486159
- Email: ssbraun@ua.edu
Study Contact Backup
- Name: Alison L Hooper, Ph.D.
- Phone Number: 205-348-0303
- Email: alhooper2@ua.edu
Study Locations
-
-
Alabama
-
Tuscaloosa, Alabama, United States, 35487
- Recruiting
- University of Alabama
-
Contact:
- Summer Braun
- Phone Number: 2053486159
- Email: ssbraun@ua.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Students in Block 3 will be invited to participate in the study.
Exclusion Criteria:
- Students who are not in Block 3 will be excluded. Participants experiencing suicidal ideations at baseline and deemed via the clinical risk assessment procedure to be at moderate or high risk of suicide will be excluded from the study after baseline, and prior to randomization.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Business as Usual
Participants in this arm will continue with daily life as usual.
|
|
|
Experimental: Healthy Minds Program
Participants in this arm engage with the Healthy Minds Program app.
|
Participants in this arm engage with the Healthy Minds Program app/
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Depression - Short Form 8b
Time Frame: Participants will report on depression at baseline, post-intervention (3 months after baseline), 3-month follow-up , and 12-month follow-up.
|
Participants will self-report on depression.
Each of the 8 items is rated on 1 (1 = Never) to 5 (5 = Always) scale.
Responses will be summed to create the raw scale score.
Higher values indicate greater symptoms of depression (i.e., a worse outcome).
|
Participants will report on depression at baseline, post-intervention (3 months after baseline), 3-month follow-up , and 12-month follow-up.
|
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety - Short Form 7a
Time Frame: Participants will report on anxiety at baseline, post-intervention (3 months after baseline), 3-month follow-up, and 12-month follow-up.
|
Participants will self-report on anxiety.
Each of the 7 items is rated on 1 (1 = Never) to 5 (5 = Always) scale.
Responses will be summed to create the raw scale score.
Higher values indicate greater symptoms of anxiety (i.e., a worse outcome).
|
Participants will report on anxiety at baseline, post-intervention (3 months after baseline), 3-month follow-up, and 12-month follow-up.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Turnover Intentions
Time Frame: Participants will report turnover intentions at 3-month follow-up, and 12-month follow-up.
|
Participants will self-report on their intentions to leave their job.
|
Participants will report turnover intentions at 3-month follow-up, and 12-month follow-up.
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Teaching Quality: edTPA
Time Frame: edTPA scores will be collected immediately after the intervention.
|
Performance-based assessment of teaching quality required for teacher certification.
Higher scores indicate greater teaching quality.
|
edTPA scores will be collected immediately after the intervention.
|
|
Teaching Quality: Candidate Preservice Assessment of Student Teaching (CPAST)
Time Frame: CPAST scores will be collected immediately after the intervention.
|
Summative assessment of pre-service teachers' teaching quality during the semester-long student teaching experience.
Higher scores indicate greater teaching quality.
|
CPAST scores will be collected immediately after the intervention.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 17, 2025
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
June 1, 2027
Study Registration Dates
First Submitted
December 12, 2024
First Submitted That Met QC Criteria
December 19, 2024
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
April 2, 2025
Last Update Submitted That Met QC Criteria
March 31, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24-01-7242
- R15MH134225 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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