Actively Recruiting
Implementing the Spotlight AQ Platform in Adolescent/ Young Adult (16-25 Years Old) Type 1 Diabetics (T1D)
Led by Children's Mercy Hospital Kansas City · Updated on 2026-01-09
60
Participants Needed
1
Research Sites
131 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to compare the Spotlight AQ survey platform to the standard of care (SOC) pre-clinic assessment in adolescents \& young adults (16-25 years old) with Type 1 Diabetes (T1D). The main questions it aims to answer are: * Does using the Spotlight AQ survey in clinic decrease the A1c in the people who use it? * Do patients and healthcare providers like using the spotlight AQ survey? Participants will use the Spotlight AQ survey before coming in to two standard of care T1D clinic visits Participants will fill out surveys describing how they feel about using the Spotlight AQ survey. Some participants may be asked to do an interview to talk about how they feel about the Spotlight AQ survey.
CONDITIONS
Official Title
Implementing the Spotlight AQ Platform in Adolescent/ Young Adult (16-25 Years Old) Type 1 Diabetics (T1D)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 16-25 years old
- Diagnosed with Type 1 Diabetes for at least 6 months
- Currently receiving any diabetes treatment
- Using a Continuous Glucose Monitor (CGM)
- Willing and able to use the Spotlight AQ survey tool
- Able to give verbal assent
- Patients and parents/caregivers speak English or Spanish fluently
- Receiving care at Children's Mercy Kansas City Hospital or Boston Children's Hospital network
You will not qualify if you...
- Younger than 16 years or older than 25 years
- Having a mental illness that seriously limits ability to participate
- Lacking capacity to participate
- Enrolled in another Type 1 Diabetes intervention study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Children's Mercy
Kansas City, Missouri, United States, 64111
Actively Recruiting
Research Team
P
Priscilla Connell, MPH
CONTACT
C
Cintya Schweisberger, DO
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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