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Implementing the Spotlight AQ Platform in Adolescent/ Young Adult (16-25 Years Old) Type 1 Diabetics (T1D) - Trial NCT06390371

Access comprehensive clinical trial information for NCT06390371 through Pure Global AI's free database. This phase not specified trial is sponsored by Children's Mercy Hospital Kansas City and is currently Recruiting. The study focuses on Type 1 Diabetes Mellitus. Target enrollment is 60 participants.

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NCT06390371
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Trial Details
ClinicalTrials.gov โ€ข NCT06390371
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Implementing the Spotlight AQ Platform in Adolescent/ Young Adult (16-25 Years Old) Type 1 Diabetics (T1D)
Spotlight AQ Randomized Controlled Trial of the Spotlight AQ Survey Platform to Evaluate Its' Efficacy and Applicability in a Clinic Setting.

Study Focus

Type 1 Diabetes Mellitus

Spotlight AQ Survey platform

Interventional

other

Sponsor & Location

Children's Mercy Hospital Kansas City

Kansas City, United States of America

Timeline & Enrollment

N/A

Jun 06, 2024

Dec 01, 2024

60 participants

Primary Outcome

HbA1c

Summary

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.

ICD-10 Classifications

Type 1 diabetes mellitus
Type 1 diabetes mellitus with unspecified complications
Type 1 diabetes mellitus with other specified complications
Type 1 diabetes mellitus without complications
Type 1 diabetes mellitus with multiple complications

Data Source

ClinicalTrials.gov

NCT06390371

Non-Device Trial