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Diabetes Mellitus, Type 2NCT05826678

Trial to Assess Continuous Glucose Monitoring in Asian Americans With Type 2 Diabetes

A study testing Continuous Glucose Monitor and Finger stick glucose monitoring in people with Diabetes Mellitus, Type 2, run by Joslin Diabetes Center at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This study aims to understand the use of continuous glucose monitors (CGM) in Asian Americans with type 2 diabetes (T2D). Researchers will compare participants on continuous glucose monitors with participants using fingerstick self-monitoring with the aim of answering the following questions: 1. Read more about this study

Who is it for?
Ages 40 years and older
Conditions the study is for
Diabetes Mellitus, Type 2
What is being tested?
Continuous Glucose Monitor and Finger stick glucose monitoring
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
30 participants
Where
1 siteUnited States
Study dates
22 Sep 2022to 31 May 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Chinese Americans 40 years and older who are 1st generation immigrants, currently residing in the US, and clinically diagnosed with T2D.
  • CGM-naïve
  • HbA1c >7.5% within 3 months of study commencement.
  • Participants should also possess a smartphone, as this is needed in order to facilitate the collection of CGM data by the study team as well as homogenize CGM usage education.

Who cannot join

  • Known diagnosis of dysfunction/dementia or learning disabilities
  • Not fluent in either English or Chinese
  • Currently undergoing or planning to undergo diathermy or high-frequency heat treatments in whom CGM use may be contraindicated
  • Inability to travel due to frailty or health reasons
  • Lack of internet access
  • Critically ill populations, including those on dialysis
  • Vulnerable populations (prisoners and women who are pregnant or planning to be pregnant during the time of study)

Trial locations and contacts

1 site in 1 country.

Atif Adam, PhD, MD, MPH contact

4103363626

atif.adam@joslin.harvard.edu

United States1 site, 1 recruiting
  • Joslin Diabetes Center

    Boston, Massachusetts, 02215

    Hetal Shah, MD, MPH, 617-309-4343, hetal.shah@joslin.harvard.edu

    George King, MD

    Recruiting

Other trials in United States

About this study

Official title: A Pilot Clinical Trial to Assess Feasibility, Facilitators and Barriers of Continuous Glucose Monitoring in Asian Americans With Type 2 Diabetes

This study aims to understand the use of continuous glucose monitors (CGM) in Asian Americans with type 2 diabetes (T2D). Researchers will compare participants on continuous glucose monitors with participants using fingerstick self-monitoring with the aim of answering the following questions:

  1. Check if continuous glucose monitoring is doable and consistent for this group, and see how it affects their quality of life.
  2. Estimate how well the health outcomes (glucose and lipid markers) vary over the study period.
  3. Understand how social and community factors can impact the use of continuous glucose monitors in this group.
Read the detailed description

The Type 2 Diabetes (T2D) pandemic continues to expand in the U.S. and globally. However, the prevalence of T2D is much higher in Asian-Americans (AA) and in other minorities compared to non-Hispanic Whites in the U.S, and AAs have the highest age- and sex-adjusted undiagnosed rate of T2D (7.5%) compared to all other ethnic and racial groups. There is ample evidence that disparities in diagnosis and care for T2D exist in AA communities. The majority of AAs are 1st generation immigrants, and this has further contributed to the disparity in care and diagnosis of diabetes due to the following reasons:

  1. Higher unawareness rate: A major contributor to higher T2D unawareness among AAs is the significant difference in BMI-associated T2D risk among AAs (24-25 kg/m2) compared with non-Asians (29-30 kg/m2). Until the "Screen at 23" campaign (See "Innovation"), no national agency would recognize and recommend that AAs be screened for T2D at lower BMIs of 23-25 kg/m2. Furthermore, NHANES data has shown that while age- and sex-adjusted diabetes prevalence among AAs is 19%, the breakdown of this figure may not be truly reflective of the actual prevalence among the disaggregated AA subgroups, which showed a wide variation with South Asians at 23%, Southeast Asians at 22%, and East Asians (including Chinese, Koreans and Japanese) at 14%, the last one being comparable to a recent report from China which showed diabetes prevalence of 11.2%.
  2. Cultural and language barriers: AAs living in the US have the highest rates (35%) of limited English proficiency. This figure is even higher at 44% for foreign-born ChA. Limited English proficiency is closely linked to reduced health access, poor health outcomes and lower utilization rates of health technologies.
  3. Model minority myth: Hurdles to health care have been significantly exacerbated by the exponential rise in anti-Asian sentiments during the COVID-19 pandemic.

Rapidly advancing diabetes technologies, especially CGM, can achieve better metabolic targets, lower diabetes-related complications, and provide a better quality of life, which have been reported for other ethnic groups but not for AAs due to the systemic exclusion of AAs from CGM studies. Multiple systemic barriers exist for AA to access CGMs, including costs and lack of data to justify reimbursement, provider inertia, and lack of advocacy and vocalization of needs, on top of limited English proficiency and lack of culturally-tailored education. These barriers are in addition to a lack of "Digital Literacy", the new "super social determinant of health", which will increase disparities between those who have skills and access to digital tools and those who do not. In this proposal, we will evaluate the impact, barriers and facilitators of CGM use and adherence in AAs (1st generation ChA) with T2D.

In this 6-month clinical trial, we will examine the impact of CGM use vs. No CGM among 1st generation ChA with T2D.The aim will be to:

  1. Evaluate feasibility (adherence and consistency) and quality of life measures during CGM use in this population.
  2. Generate precision estimates of the distribution of the secondary outcomes (6-month glycemic control and lipid markers) in both arms to inform a future randomized controlled trial (RCT).

3: Identify multi-level barriers and facilitators of CGM use for ChA with T2D, using a socioecological framework (patient-level, provider-level, and community/environment level). We aim to comprehensively evaluate the implementation process (facilitators and impediments), resource requirements, and intermediate patient adherence outcomes for the program using mixed-methods approaches. These will inform the design of culturally-tailored interventions for larger RCT.

Being tested
Continuous Glucose Monitor, Finger stick glucose monitoring
Keywords
Continuous Glucose Monitoring, Health Disparity
Medical subject headings
Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Continuous Glucose MonitorDevice

    The Clinical Diabetes Educator (CDE) will follow up with the participants at Month 1 after the baseline study visit, at the study midpoint (Month 3), and at the end of the study (Month 6) to check CGM usage, including timely calibration and change adherence. At the end of the study, participants will be invited to complete a survey and participate in virtual interviews to assess changes in their health behaviors and the acceptability of CGM devices.

  • Finger stick glucose monitoringBehavioural

    Participants will adhere to the standard care protocol and continue self-monitoring of blood glucose through fingersticks as per usual practice[46]. The Clinical Diabetes Educator (CDE) will monitor and provide follow-up to the control group participants as per the same schedule followed for the intervention group.

Study groups in NCT05826678
Study groupRoleWhat they receive
Participants on CGMActive comparatorParticipants in this group will be offered a CGM device for glucose monitoring, with training and educational materials provided in either English or Chinese, according to the participant's preference.
Receives: Device: Continuous Glucose Monitor
Participants on Finger-stick onlyPlacebo comparatorParticipants in this group continue standard fingerstick self-monitoring of blood glucose (FSGM) as per standard care protocol. They will also receive educational materials provided in either English or Chinese, according to the participant's preference.
Receives: Behavioral: Finger stick glucose monitoring

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Feasibility (CGM device adherence)

    Number of hours device is active in total for the entire 6 month study period

    Measured: 6 month

  2. Feasibility (Consistency) 1

    Proportion CGM program elements completed at each visit against a checklist of pre-specified essential elements

    Measured: 6 months

  3. Feasibility (Consistency) 2

    Average session duration as compared to assigned time plan.

    Measured: 6 months

  4. World Health Organization (Five) Well-Being Index (WHO-5) change over 6 month study period

    WHO-5 uses a five-item scale to assess overall well-being

    Measured: Change in measure comparing Baseline and 6 months

  5. EQ-5D-5L change over 6 month study period

    EQ-5D-5L assesses health status both as an overall self-rated health on a visual analog scale and across five areas (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) with three levels of severity (no/mild, moderate, or severe problems)

    Measured: Change in measure comparing Baseline and 6 months

  6. Diabetes Distress Scale (DDS) change over 6 month study period

    DDS is a 17-item scale that measures worry and concerns specifically related to diabetes and its management

    Measured: Change in measure comparing Baseline and 6 months

  7. Hypoglycemic Confidence Scale (HCS) change over 6 month study period

    HCS is a nine-item survey that evaluates the degree to which patients feel able, secure, and comfortable about their ability to stay safe from hypoglycemic-related problems

    Measured: Change in measure comparing Baseline and 6 months

Secondary outcomes (7)
  1. HbA1c change (%) from 0-6 months

    HbA1c change (%) between baseline (0 months) and end of intervention period (6 months) will be assessed as a continuous response variable for each study arm

    Measured: Change in measure comparing Baseline and 6 months

  2. Time in range (TIR) metrics change (%) from 0-6 months

    Change in %TIR metrics between baseline (0 months) and end of intervention period (6 months) will be assessed as a continuous response variable for the CGM+ arm

    Measured: Change in measure comparing Baseline and 6 months

  3. Lipid changes from 0-6 months

    We plan to assess the changes from baseline to 6 months for levels of lipid profile components, including total cholesterol, triglyceride, low-density lipoprotein (LDL), and high-density lipoprotein (HDL) levels.

    Measured: Change in measure comparing Baseline and 6 months

  4. Blood pressure changes from 0-6 months

    We will assess change from baseline to 6 months for systolic and diastolic blood pressures.

    Measured: Change in measure comparing Baseline and 6 months

  5. eGFR changes from 0-6 months

    We will assess change from baseline to 6 months for eGFR

    Measured: Change in measure comparing Baseline and 6 months

  6. Diabetes Knowledge and Behavior change from 0-6 months

    Assessed through Semi-structured virtual interviews that will be conducted at the Baseline and 6-month mark.

    Measured: Change comparing Baseline and 6 months

  7. Family/social-level factors impacting technological device for care management

    Semi-structured virtual interviews conducted at baseline and 6-month mark (in both arms) will also probe participants on broad topics of stigmas related to technology will be assessed with more directed questions on stigmas in varying environments-home, work, and in social gatherings.

    Measured: Change comparing Baseline and 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Apr 2023
  2. Study start22 Sep 2022
  3. Primary completion15 May 2024 (estimated)
  4. Study completion31 May 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05826678
Sponsor's protocol ID
STUDY00000206
Status last verified
Mar 2024
First submitted
12 Apr 2023
Last updated
15 Mar 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Continuous Glucose Monitor and Finger stick glucose monitoring in people with Diabetes Mellitus, Type 2, run by Joslin Diabetes Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 15 Mar 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Hetal Shah, MD, MPH (617-309-4343, hetal.shah@joslin.harvard.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Feasibility (CGM device adherence) (time frame: 6 month). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Mar 2024.

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