Calorie Reduction Or Surgery: Seeking Remission for Obesity And Diabetes (CROSSROADS)
Primary Purpose
Diabetes Mellitus, Type 2, Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
laparoscopic Roux-en-Y gastric bypass (RYGB) procedure
Lifestyle Intervention
Sponsored by

About this trial
This is an interventional treatment trial for Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion Criteria:
- currently enrolled at Group Health
- currently enrolled in a GH insurance product that provides coverage for laparoscopic gastric bypass (e.g., Medicare, PEBB, or has GH bariatric coverage rider)
- age on January 1, 2011 will be between 25 and 65 years
Diabetes: must meet one or more of the following criteria during the past two years (10/1/08 - 9/30/10):
- 1+ fills for a diabetes-specific medication (oral or insulin)
- Hemoglobin A1c ≥7.0% on one or more occasions
- Fasting Blood glucose ≥126 mg/dL on two or more occasions [separate days]
- Random glucose ≥200 mg/dl on two or more occasions [separate days]
- One fasting blood glucose ≥126 mg/dL plus one random glucose ≥200 mg/dl [must occur on separate days]
- One or more inpatient (primary or secondary hospital discharge) code related to diabetes. See list below.
- Two or more outpatient ICD-9 codes related to diabetes (ambulatory visits (AV) only - not telephone, email, emergency department, lab, radiology, or other (IS, OE) encounter types) [Two visits must occur on separate days]
- Obesity: All patients must have a body mass index [BMI] between 30 and <40kg/m2; weight measurement must be within the past two years (10/1/08 - 9/30/10)
Exclusion Criteria:
- Pregnancy within the past one year (10/1/09 - 9/30/10)
Excluded if the following conditions are recorded within the past two years (10/1/08 - 9/30/10):
- malignant tumor
- ascites
- peritoneal effusion
- cirrhosis
- schizophrenia
- schizoaffective disorder
- bipolar disorder
- dementia
- HIV
- inflammatory bowel disease
- dialysis
Exclude if occurred between 1/1/95 - 9/30/10:
- Any prior bariatric or major gastrointestinal operation
- Any prior liver, heart, intestinal, and/or lung transplant
Sites / Locations
- Group Health Research Institute
- Fred Hutchinson Cancer Research Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Lifestyle Intervention
Surgery
Arm Description
Outcomes
Primary Outcome Measures
Feasibility
Explore the feasibility of a set of novel methods to create an appropriate randomization cohort of patients with type 2 diabetes mellitus (T2DM) and a body mass index (BMI) of 30-40 kg/m2 who are willing to be randomized into either roux-en-Y gastric bypass (RYGB) surgery or an intensive medical/lifestyle intervention. This will be assessed by comparing the number of people recruited to the number randomized and subsequently enrolled in the study.
Secondary Outcome Measures
Efficacy and Mechanisms
Participants will complete research visits at Baseline, 6-month and 12-month. Both intervention groups (surgery and lifestyle) will complete the same physical assessments to compare success of the intervention. Physical measures include a fasting blood draw, DEXA scan, exercise treadmill test, anthropometric measures and vitals. Additionally, a subset of participants will be assessed for changes in their immune system before and after the intervention. Measures include an adiopose tissue biopsy and an Oral Glucose Tolerance Test.
Full Information
NCT ID
NCT01295229
First Posted
February 2, 2011
Last Updated
March 29, 2016
Sponsor
University of Washington
Collaborators
Kaiser Permanente, Fred Hutchinson Cancer Center, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT01295229
Brief Title
Calorie Reduction Or Surgery: Seeking Remission for Obesity And Diabetes
Acronym
CROSSROADS
Official Title
Feasibility, Efficacy, and Mechanisms of Surgical vs Medical Diabetes Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Kaiser Permanente, Fred Hutchinson Cancer Center, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The escalating pandemics of obesity and type 2 diabetes mellitus (T2DM) are among the most significant contributors to morbidity and mortality worldwide. Roux-en-Y gastric bypass (RYGB) surgery causes profound weight loss and dramatically ameliorates T2DM through mechanisms beyond just weight loss, but its role in diabetes management and the nature of its weight-independent anti-diabetes effects are not well established because of a paucity of appropriate randomized trials, the execution of which is hindered by numerous obstacles. The investigators therefore propose a feasibility study to demonstrate our capacity to identify, recruit, randomize, and track outcomes for 40 adult Group Health members identified as having T2DM and a BMI between 30-40 kg/m2.
Detailed Description
The overall goal of the research study is to demonstrate our capacity to identify, recruit, randomize, and track outcomes for 40 adult Group Health members identified as having T2DM and a BMI between 30-40 kg/m2.
Our cohort recruitment strategy will utilize the GH administrative and clinical databases to identify patients with T2DM and a BMI of 30-40 kg/m2. Sufficient numbers (N=4,000) of these individuals will be mailed and surveyed to identify the small minority without strong preferences regarding medical vs. surgical diabetes/obesity treatment. This subset will be invited to become better informed about both strategies using a novel, standardized patient decision aid for shared decision making (SDM) related to bariatric surgery: a high-quality educational video that provides balanced and frequently updated information about the risks and benefits of surgical and non-surgical care. After viewing SDM tool, potential subjects' "willingness to randomize" will be assessed, and a subset of willing patients will actually undergo randomization to either RYGB or a state-of-the-art intensive but reproducible medical/lifestyle intervention.
Forty patients will be randomized to either RYGB or an intensive medical/lifestyle intervention. Twenty members will be randomly assigned to intensive behavioral/medical treatment, and twenty will be randomly assigned to receive gastric bypass surgery. In the non-surgical group, the investigators will study the feasibility and resources needed to deploy a state-of-the-art intensive behavioral intervention to promote weight loss, which includes dietary and exercise components. It will be coupled with diabetes pharmacotherapy treatment consistent with Group Health Clinical Practice Guidelines (http://incontext.ghc.org/clinical/clin_topics/diabetes2/dm2_poc.html).
Patients randomized to the surgical arm will undergo a standard laparoscopic proximal RYGB, as commonly practiced by GH surgeons. The operation and post-operative care will be performed at GH by Dr. Steven Bock, Dr. Jeffery Lander, and their clinical staff, including a team of nutritionists and a Registered Nurse Case Manager who coordinates the care of patients in the GH Bariatric Surgery Program. Surgical patients will also undergo a standardized 8-week pre-operative and 10-month post-operative behavioral treatment regimen with the GH Bariatric Surgery Program.
Participants will have follow-up research visits at 3, 6, 9, and 12 months after randomization, where they will have the following measurements: standardized physically exam by Dr. Foster-Schubert; weight, waist and hip circumferences; systolic and diastolic blood pressure; resting 1-minute pulse; and fasting (12-hour) blood (50 ml) collection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Obesity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
43 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lifestyle Intervention
Arm Type
Active Comparator
Arm Title
Surgery
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
laparoscopic Roux-en-Y gastric bypass (RYGB) procedure
Other Intervention Name(s)
weight loss surgery, bariatric surgery
Intervention Description
The laparoscopic Roux-en-Y gastric bypass (RYGB) procedure is the most commonly performed bariatric procedure in the United States. Patients randomized to the surgical arm will undergo a standard laparoscopic proximal RYGB, as commonly practiced by GH surgeons, using a 90-cm alimentary limb, 50-cm biliopancreatic limb, antecolic/antegastric approach, and totally stapled technique.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle Intervention
Other Intervention Name(s)
Diet and Exercise Program
Intervention Description
The lifestyle intervention includes behavior-modification skills counseling combined with training in diet and exercise change. The focus of the exercise intervention is a gradual increase in brisk walking or other activities of similar moderate aerobic intensity. The exercise prescription will consist of at least 45 minutes of exercise, 5 days per week for 12 months. The diet intervention will be conducted by a research dietician with training in behavior modification, with supervision by Dr. Foster-Schubert. In week 1 the dietician will meet for a 60-minute individual session with participants at the FHCRC Prevention Center. Over the next 23 weeks the dietician will conduct one 30-minute group session per week.
Primary Outcome Measure Information:
Title
Feasibility
Description
Explore the feasibility of a set of novel methods to create an appropriate randomization cohort of patients with type 2 diabetes mellitus (T2DM) and a body mass index (BMI) of 30-40 kg/m2 who are willing to be randomized into either roux-en-Y gastric bypass (RYGB) surgery or an intensive medical/lifestyle intervention. This will be assessed by comparing the number of people recruited to the number randomized and subsequently enrolled in the study.
Time Frame
April 2011 - January 2012
Secondary Outcome Measure Information:
Title
Efficacy and Mechanisms
Description
Participants will complete research visits at Baseline, 6-month and 12-month. Both intervention groups (surgery and lifestyle) will complete the same physical assessments to compare success of the intervention. Physical measures include a fasting blood draw, DEXA scan, exercise treadmill test, anthropometric measures and vitals. Additionally, a subset of participants will be assessed for changes in their immune system before and after the intervention. Measures include an adiopose tissue biopsy and an Oral Glucose Tolerance Test.
Time Frame
April 2011-April 2013
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
currently enrolled at Group Health
currently enrolled in a GH insurance product that provides coverage for laparoscopic gastric bypass (e.g., Medicare, PEBB, or has GH bariatric coverage rider)
age on January 1, 2011 will be between 25 and 65 years
Diabetes: must meet one or more of the following criteria during the past two years (10/1/08 - 9/30/10):
1+ fills for a diabetes-specific medication (oral or insulin)
Hemoglobin A1c ≥7.0% on one or more occasions
Fasting Blood glucose ≥126 mg/dL on two or more occasions [separate days]
Random glucose ≥200 mg/dl on two or more occasions [separate days]
One fasting blood glucose ≥126 mg/dL plus one random glucose ≥200 mg/dl [must occur on separate days]
One or more inpatient (primary or secondary hospital discharge) code related to diabetes. See list below.
Two or more outpatient ICD-9 codes related to diabetes (ambulatory visits (AV) only - not telephone, email, emergency department, lab, radiology, or other (IS, OE) encounter types) [Two visits must occur on separate days]
Obesity: All patients must have a body mass index [BMI] between 30 and <40kg/m2; weight measurement must be within the past two years (10/1/08 - 9/30/10)
Exclusion Criteria:
Pregnancy within the past one year (10/1/09 - 9/30/10)
Excluded if the following conditions are recorded within the past two years (10/1/08 - 9/30/10):
malignant tumor
ascites
peritoneal effusion
cirrhosis
schizophrenia
schizoaffective disorder
bipolar disorder
dementia
HIV
inflammatory bowel disease
dialysis
Exclude if occurred between 1/1/95 - 9/30/10:
Any prior bariatric or major gastrointestinal operation
Any prior liver, heart, intestinal, and/or lung transplant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David E Cummings, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David R Flum, MD, MPH
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Group Health Research Institute
City
Seattle
State/Province
Washington
ZIP/Postal Code
98101
Country
United States
Facility Name
Fred Hutchinson Cancer Research Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98109
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
28722299
Citation
Banerjee S, Garrison LP Jr, Flum DR, Arterburn DE. Cost and Health Care Utilization Implications of Bariatric Surgery Versus Intensive Lifestyle and Medical Intervention for Type 2 Diabetes. Obesity (Silver Spring). 2017 Sep;25(9):1499-1508. doi: 10.1002/oby.21927. Epub 2017 Jul 19.
Results Reference
derived
PubMed Identifier
26983924
Citation
Cummings DE, Arterburn DE, Westbrook EO, Kuzma JN, Stewart SD, Chan CP, Bock SN, Landers JT, Kratz M, Foster-Schubert KE, Flum DR. Gastric bypass surgery vs intensive lifestyle and medical intervention for type 2 diabetes: the CROSSROADS randomised controlled trial. Diabetologia. 2016 May;59(5):945-53. doi: 10.1007/s00125-016-3903-x. Epub 2016 Mar 17.
Results Reference
derived
Learn more about this trial
Calorie Reduction Or Surgery: Seeking Remission for Obesity And Diabetes
We'll reach out to this number within 24 hrs