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Strengthening Health and Insight in New Educators

Healthy Minds for Pre-Service Teachers

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06745934
Acronym
SHINE
Enrollment
140
Registered
2024-12-20
Start date
2025-01-17
Completion date
2027-06-30
Last updated
2025-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Symptoms, Depressive Symptoms

Keywords

Healthy Minds Program, mindfulness-based intervention, app, pre-service teachers, mental health

Brief summary

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.

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.

Interventions

Participants in this arm engage with the Healthy Minds Program app/

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Alabama, Tuscaloosa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Patient-Reported Outcomes Measurement Information System (PROMIS) Depression - Short Form 8bParticipants 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).
Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety - Short Form 7aParticipants 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).

Secondary

MeasureTime frameDescription
Turnover IntentionsParticipants 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.

Other

MeasureTime frameDescription
Teaching Quality: edTPAedTPA scores will be collected immediately after the intervention.Performance-based assessment of teaching quality required for teacher certification. Higher scores indicate greater teaching quality.
Teaching Quality: Candidate Preservice Assessment of Student Teaching (CPAST)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.

Countries

United States

Contacts

Primary ContactSummer S Braun, Ph.D.
ssbraun@ua.edu2053486159
Backup ContactAlison L Hooper, Ph.D.
alhooper2@ua.edu205-348-0303

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026