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New treatment option for Type 2 Diabetes
Official title Implementing an Effective Diabetes Intervention Among Low-Income Immigrants
ClinicalTrials.gov ID: NCT06319703
What this study is testing
- What it's testing
- 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.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 70
You may be able to join if
- 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;
You likely can't join if
- unable or unwilling to provide informed consent;
- unable to participate meaningfully in the intervention (e.g., uncorrected sight and hearing impairment);
- 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).
See the full eligibility criteria
- 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.
- unable or unwilling to provide informed consent;
- unable to participate meaningfully in the intervention (e.g., uncorrected sight and hearing impairment);
- 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).
The study team makes the final eligibility decision.
Where it's taking place
- New York, New York, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 70 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include New York, New York, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.