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AIManage Using an AI-driven CDS and Chatbot

AIManage: Using an AI-driven CDS and Chatbot for the Management of Patients on Incretin Mimetic Medications

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07546357
Enrollment
16
Registered
2026-04-22
Start date
2026-06-01
Completion date
2029-03-30
Last updated
2026-04-22

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

Conditions

Diabetes, Medication Side Effects, Obesity

Keywords

GLP-1, Incretin mimetic, medication management, side effect management

Brief summary

The objective of this project is to define and test the GenAI-powered Clinical Decision Support (CDS) tool, AIManage, providing a broad range of incretin mimetic medication management services to optimize dose titrations. The study will take place across primary care and obesity medicine clinics at NYUH. The study is currently conducting formative data collection for tool refinement (Phase 1). Once completed, a cluster randomized controlled trial of the AIManage tool will be undertaken (Phase 2).

Interventions

OTHERAIManage

GenAI-powered CDS tool that provides a range of IMM management services, such as personalized guidance for patients on side effects management and clinical advisement to optimize dose titrations.

Sponsors

NYU Langone Health
Lead SponsorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

Provider Eligibility Criteria (Phase 1) * Primary or bariatric care provider (MD/DO, NP) practicing at the participating NYULH clinics, * Provide care to at least 5 patients prescribed an IMM. Patient Eligibility Criteria (Phase 1) * (Phase 1) Currently taking an IMM or have taken an IMM in the past 6 months; * Fluency in English or Spanish; * Be willing to send/receive text messages; and * Be \> 18 years of age.

Exclusion criteria

Provider

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Patients who Complete Qualitative Measure - Perceived UsefulnessDay 1 (60 minutes)In Phase 1, qualitative data regarding perceived usefulness will be collected.
Percentage of Patients who Complete Qualitative Measure - Perceived UsabilityDay 1 (60 minutes)In Phase 1, qualitative data regarding perceived usability will be collected.
Percentage of Patients who Complete Qualitative Measure - Perceived Use ChallengesDay 1 (60 minutes)In Phase 1, qualitative data regarding perceived use challenges will be collected.
Percentage of Patients who Complete Qualitative Measure - Perceived ValueDay 1 (60 minutes)In Phase 1, qualitative data regarding perceived value will be collected.

Countries

United States

Contacts

CONTACTElizabeth Stevens, PhD, MPH
Elizabeth.Stevens@nyulangone.org646-501-2558
PRINCIPAL_INVESTIGATORElizabeth Stevens, PhD, MPH

NYU Langone Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 23, 2026