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NCT06319703Recruiting

Implementing an Effective Diabetes Intervention Among Low-Income Immigrants

IDEAL: Implementing an Effective Diabetes intervEntion Among Low-income Immigrants

Source: ClinicalTrials.gov · Last updated 9 Mar 2026

Brief summary (registry, in English)

The goal of this IDEAL project is to examine the effectiveness and implementation process of the video-based Diabetes Self-Management Education and Support (DSMES) + community health worker (CHW) (hereafter: "IDEAL") intervention compared with a wait-list control group (hereafter: "CONTROL") to improve glycemic control among Chinese immigrants with Type 2 diabetes (T2D) in New York City (NYC). Participants will be randomized with equal allocation to one of the 2 groups. The IDEAL group will receive 1 DSMES brief video/week for 24 weeks delivered via text message. The CHW will assess participants' SDOH barriers to T2D care and link them to available resources in the community. The CONTROL group will continue to receive their usual care and at the end of the study, they will receive DSMES videos.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
270 (estimated)
First submitted
13 Mar 2024
Start date
29 Dec 2024
Primary completion date
31 Dec 2027
Lead sponsor
NYU Langone Health
NCT number
NCT06319703

What you commit to

  • Study type: Interventional
  • Planned participants: 270
  • From 29 Dec 2024 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • unable to participate meaningfully in the intervention (e.g., uncorrected sight and hearing impairment);

Other

  • unable or unwilling to provide informed consent;
  • unwilling to accept randomization assignment;
  • is pregnant, plans to become pregnant in the next 6 months, or becomes pregnant during the study, or
  • is breastfeeding (e.g., they may have potential dietary restrictions).

Who the study is looking for

  • Participants must:
  • self-identify as a Chinese immigrant;
  • be between 18-70 years old,
  • have a diagnosis of T2D in the medical record;
  • have had an appointment with a physician for routine T2D care within the past 12 months;
  • have a most recent HbA1c \> or = 8%;
  • be willing to receive brief videos regarding T2D management, and
  • possess a smartphone or, if they do not have one, be willing and able to use a study smartphone.

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
NYU Langone Health
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.