Mindfulness App to Help Teachers with Anxiety and Depression
Strengthening Health and Insight in New Educators
Recruiting
N/A
Interventional Study
Anxiety Symptoms
Depressive Symptoms
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 140 (estimated)
- Sponsor
- University of Alabama, Tuscaloosa · Other
Who this trial is looking for
This trial is looking for teachers in their final year of training who want to improve their mental health. Participants will use a mindfulness app designed to help reduce feelings of anxiety and depression during their transition into teaching.
Are You a Good Fit for This Trial?
You may be able to join if
- I am a student in Block 3.
You may not be able to join if
- I am not a student in Block 3.
- I have had thoughts of suicide and am considered at moderate or high risk.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
About This Trial
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 ass…
Trial Locations
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Eligibility Criteria
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 r…
Contacts