School Nurse-Led Program for Early Anxiety Detection
Grow With Grit: A School Nurse-Led SBIRT Pilot for Early Anxiety Detection
Recruiting
N/AInterventional Study
Anxiety
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
8 – 12
Sex
Any
Study type
Interventional
Purpose
Screening
Participants needed
60 (estimated)
Sponsor
McLaughlin Research Institute for Biomedical Sciences, Inc. · Other
Who this trial is looking for
This trial is looking for students aged 8-12 who may have anxiety. If selected, I will answer some questions about my feelings and receive support if needed.
Are You a Good Fit for This Trial?
Rules you outActive cancer treatmentEpilepsyDiabetesSickle cell diseaseAsthma with frequent issues
You may be able to join if
I am a GFPS student aged 8-12.
I attend Mountain View Elementary, West Elementary, Longfellow Elementary, or Sunnyside Elementary.
I have visited the school nurse three or more times for physical symptoms like stomach aches or headaches in the past 6 weeks.
I have missed 10% or more of school days due to these physical symptoms.
I speak English without needing an interpreter.
You may not be able to join if
I am currently receiving ongoing behavioral health services like therapy or medication.
I have a chronic medical condition that explains my repeated visits to the school nurse.
I have a documented cognitive or communication issue that makes it hard to complete required questionnaires.
I am a ward of the state or in foster care.
I am not an English speaker.
I have acute safety concerns like suicidal thoughts or a recent attempt.
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 a few quick questions to see if you may meet the eligibility requirements.
All enrolled students and their parents or guardians will complete baseline anxiety questionnaires. Students with a positive baseline screen will receive a brief school nurse-delivered coping skill, referral support when indicated, and follow-up assessments at approximately three and six months. Students with a negative screen will not enter the intervention and follow-up phase.
Trial Locations
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Facility
City
State
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Status
Eligibility Criteria
Inclusion Criteria:
1. GFPS students aged 8-12 years and enrolled at one of the following schools:
Mountain View Elementary West Elementary Longfellow Elementary Sunnyside Elementary School
2. Participants will be identified through a weekly review of school nurse electronic health records (Fro…
Inclusion Criteria:
1. GFPS students aged 8-12 years and enrolled at one of the following schools:
Mountain View Elementary West Elementary Longfellow Elementary Sunnyside Elementary School
2. Participants will be identified through a weekly review of school nurse electronic health records (Frontline EHR) and attendance logs, and will include students who have either:
1. Three or more nurse visits for somatic complaints within the past 6 weeks. For this study, somatic complaints are defined as the following physical symptoms that are not otherwise linked to exclusionary illness or chronic medical processes: stomach aches, headaches, fatigue, \& generalized muscle aches.
2. Absenteeism greater than or equal to 10% of total school days due to the previously defined somatic complaints, within the past 6 weeks.
3. English-speaking without an interpreter (both student and guardian).
Exclusion Criteria
1. Currently receiving ongoing behavioral health services, including psychotherapy, psychiatric medication management, or active behavioral health case management.
1. Brief, one-time crisis counseling is not considered ongoing services.
2. Questions about eligibility should be directed to the Principal Investigator.
2. Presence of a chronic medical diagnosis that fully accounts for the student's repeated somatic visits (e.g., asthma with frequent exacerbations, epilepsy, diabetes, sickle cell disease, or active cancer treatment).
a. Students with partially explained symptoms who are also suspected to have co-occurring anxiety may be reviewed on a case-by-case basis by the PI/designee.
3. Documented cognitive or communication impairments that preclude meaningful completion of the SCARED screening tool or informed assent.
1. Examples include moderate to severe intellectual disability or severe receptive/expressive language disorder without feasible accommodations.
2. Students with an IEP or 504 plan that includes communication supports may be included if they can complete the tool with reasonable accommodations.
4. Students who are wards of the state or in foster care.
5. Non-English speaking students or guardians.
6. Acute safety concerns at the time of screening (e.g., active suicidal ideation with plan/intent, recent suicide attempt, or other crisis requiring immediate intervention).
1. Such students will be triaged to crisis protocols and excluded from study participation at that time.
Contacts
Donna Sanders R Principal Investigator, DNP-PMH, BSN
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