Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05884775

Novel Digital Patient-Reported Outcomes Tool for Diabetes Management

Led by NYU Langone Health · Updated on 2026-04-09

353

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Investigators will conduct a hybrid type 1 effectiveness-implementation randomized controlled trial (RCT) to evaluate the effectiveness of iMatter2 versus usual care on reduction in HbA1c at 12-months (primary outcome) among patients with Type 2 diabetes (T2D).

CONDITIONS

Official Title

Novel Digital Patient-Reported Outcomes Tool for Diabetes Management

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a full-time primary care provider (MD/DO, NP) practicing at participating family health centers or faculty group practices and provide care to at least five patients with Type 2 Diabetes
  • Have a diagnosis of Type 2 Diabetes for 6 months or more
  • Have uncontrolled Type 2 Diabetes with HbA1c greater than 7% documented on at least two visits in the past year
  • Be fluent in English or Spanish
  • Be willing to send and receive text messages
  • Be 18 years of age or older
Not Eligible

You will not qualify if you...

  • Refuse or are unable to provide informed consent
  • Have acute renal failure, end stage renal disease (ESRD), dialysis, renal transplantation, or other ESRD-related services
  • Have significant psychiatric conditions or substance abuse as documented in medical records
  • Are pregnant or planning to become pregnant within 12 months
  • Currently participate in another Type 2 Diabetes study
  • Plan to discontinue care at the clinic within the next 12 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

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Research Team

P

Priscilla D'antico

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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