A Trial of Meal Replacement at a Community Diabetes Clinic Serving a Low Socioeconomic Hispanic Population
Primary Purpose
Type 2 Diabetes, Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Meal Replacement
Standard Care
Sponsored by

About this trial
This is an interventional treatment trial for Type 2 Diabetes focused on measuring Type 2 diabetes, Obesity, Insulin, Hispanic, Low-income, Meal replacement
Eligibility Criteria
Inclusion Criteria:
Demographic
- Age >18 years
- Enrolled in the Roybal Diabetes Management Clinic
- Self-described as Hispanic
- Willing and able to participate in Spanish language group sessions.
- Willing and able to attend study visits for the duration of the study at the allocated times.
- Willing and able to maintain a food exercise and medication log and perform and record self-monitoring of blood glucose (SMBG) Clinical
- T2DM diagnosed by fasting blood glucose >126mg/dL or random blood glucose >200mg/dL
- BMI>30 kg/m2
- If a woman of childbearing potential, using effective contraception. Biochemical HbA1c 8%-12% Medication
- On insulin therapy
Exclusion Criteria:
Medical conditions
- Type 1 DM
- Illness likely to lead to unstable weight or altered glucose control.
- Proliferative diabetic retinopathy on eye examination within the last 6 months.
- Gallstones suspected on clinical history or documented on ultrasound.
- Serum creatinine >1.5mg/dL
- Symptomatic cardiovascular disease
- Documented liver disease other than fatty liver
- Lactating, pregnant or intending to become pregnant within the following year Psycho-social conditions
- Inability or unwillingness to participate in a Spanish-language lifestyle group.
- Eating disorder such as bulimia
- Uncontrolled psychiatric disorder such as severe uncontrolled depression or bipolar disorder.
- Inability to attend scheduled appointments regularly for the duration of the study Medication use
- Use of weight loss medication within previous 3 months including exenatide.
- Use of medication (other than diabetes medication) likely to lead to unstable weight or altered glucose control
- Laxative or substance abuse
- More than 10 alcoholic drinks/week
Sites / Locations
- Roybal Diabetes Management Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Meal Replacement
Standard Care
Arm Description
Meal Replacements will be provided to participants randomized to the MR group
Standard Care participants will receive standard care but no meal replacements
Outcomes
Primary Outcome Measures
Change in BMI
Secondary Outcome Measures
Severe Hypoglycemic Events
Full Information
NCT ID
NCT01729117
First Posted
November 13, 2012
Last Updated
November 13, 2012
Sponsor
University of Southern California
1. Study Identification
Unique Protocol Identification Number
NCT01729117
Brief Title
A Trial of Meal Replacement at a Community Diabetes Clinic Serving a Low Socioeconomic Hispanic Population
Official Title
The 1,2,3 Plan: A Randomized Controlled Trial of Meal Replacement With a Lifestyle Modification Program vs. Standard Care at a Community Diabetes Clinic Serving a Low Socioeconomic Hispanic Population
Study Type
Interventional
2. Study Status
Record Verification Date
November 2012
Overall Recruitment Status
Completed
Study Start Date
May 2009 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Southern California
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background and Rationale Research studies have shown that patients with type 2 diabetes (T2DM) who lose weight have better glucose control and less risk for heart disease. It has been difficult to achieve these results in a non-research setting. Meal replacements (MR) are pre-packaged meals with appropriate calories and nutrients that enhance adherence to a weight loss program by reducing decision-making and facilitating target caloric intake. The University of Southern California (USC) arm of the NIH funded Look AHEAD study at Roybal Clinic has demonstrated acceptability and success of MRs in conjunction with a structured lifestyle modification program in achieving weight loss in underserved Hispanic T2DM patients.
Objectives Our short-term objective is to determine the efficacy, safety and feasibility of a 3-month full MR program in conjunction with a 1 year standardized lifestyle modification program in a clinic setting. Our longer-term goal is to acquire data for sample size and power estimates for a larger NIH- or other funded prospective, randomized trial.
Study Methodology A 1-year, prospective trial study of 30 obese subjects with T2DM treated with insulin randomized to 2 groups: standard care (SC) or Meal Replacement group (MR). The SC will receive usual care at Roybal Diabetes Management Clinic (DMC). The MR will receive MRs and a lifestyle course in addition to the usual clinical care at the Roybal DMC. Phase 1 consists of 3-months 1200 -1400cal diet using full MR. Phase 2 consists of a 3-month transition to the same caloric intake using regular meals and 1 MR/day . Phase 3 consists of a 6-month weight loss maintenance period with 1 MR/day. This will be about 1400-1600 calories/day for women and 1800 to 2000 calories/day for men. Individual and group educational, support and counseling visits will be components of all 3 phases of the study.
Outcomes Efficacy of the program will be determined by weight, waist measurement and waist to hip ratio, blood pressure, HbA1c, lipids, and medication use at baseline and at 3, 6, 9 and 12 months. These are all measurements that are done routinely in these patients. Safety will be determined by monitoring of adverse events.
Data Analysis We will compare the outcomes between the SC and MR at 0,3,6,9 and 12 months to determine if there is evidence that the intervention improves outcomes and is safe.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Obesity
Keywords
Type 2 diabetes, Obesity, Insulin, Hispanic, Low-income, Meal replacement
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Meal Replacement
Arm Type
Other
Arm Description
Meal Replacements will be provided to participants randomized to the MR group
Arm Title
Standard Care
Arm Type
Other
Arm Description
Standard Care participants will receive standard care but no meal replacements
Intervention Type
Other
Intervention Name(s)
Meal Replacement
Other Intervention Name(s)
HMR70 Plus products; HMR Boston, Massachusetts
Intervention Description
5 Meal Replacements/day will be given for 3 months and then 1/day for 9 months.
Intervention Type
Other
Intervention Name(s)
Standard Care
Intervention Description
Standard Care only
Primary Outcome Measure Information:
Title
Change in BMI
Time Frame
12months
Secondary Outcome Measure Information:
Title
Severe Hypoglycemic Events
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Demographic
Age >18 years
Enrolled in the Roybal Diabetes Management Clinic
Self-described as Hispanic
Willing and able to participate in Spanish language group sessions.
Willing and able to attend study visits for the duration of the study at the allocated times.
Willing and able to maintain a food exercise and medication log and perform and record self-monitoring of blood glucose (SMBG) Clinical
T2DM diagnosed by fasting blood glucose >126mg/dL or random blood glucose >200mg/dL
BMI>30 kg/m2
If a woman of childbearing potential, using effective contraception. Biochemical HbA1c 8%-12% Medication
On insulin therapy
Exclusion Criteria:
Medical conditions
Type 1 DM
Illness likely to lead to unstable weight or altered glucose control.
Proliferative diabetic retinopathy on eye examination within the last 6 months.
Gallstones suspected on clinical history or documented on ultrasound.
Serum creatinine >1.5mg/dL
Symptomatic cardiovascular disease
Documented liver disease other than fatty liver
Lactating, pregnant or intending to become pregnant within the following year Psycho-social conditions
Inability or unwillingness to participate in a Spanish-language lifestyle group.
Eating disorder such as bulimia
Uncontrolled psychiatric disorder such as severe uncontrolled depression or bipolar disorder.
Inability to attend scheduled appointments regularly for the duration of the study Medication use
Use of weight loss medication within previous 3 months including exenatide.
Use of medication (other than diabetes medication) likely to lead to unstable weight or altered glucose control
Laxative or substance abuse
More than 10 alcoholic drinks/week
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth O Beale, MD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
Roybal Diabetes Management Clinic
City
Los Angeles
State/Province
California
ZIP/Postal Code
90022
Country
United States
12. IPD Sharing Statement
Learn more about this trial
A Trial of Meal Replacement at a Community Diabetes Clinic Serving a Low Socioeconomic Hispanic Population
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