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Midwest Diet and Exercise Trial (M-DEx)

Primary Purpose

Weight Loss, Obesity, Body Weight

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Portion Controlled Meals (PCM)
Group Phone (GP)
Conventional Diet
Individual Phone (IP)
Enhanced Usual Care (EUC)
Sponsored by
University of Kansas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Weight Loss

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Body mass index 25 to 45 kg/m2
  • Clearance from primary care physician

Exclusion Criteria:

  • Unable to participate in moderate intensity physical activity
  • Participation in weight loss or physical activity program in previous 6 months
  • Greater than 3, 30-min bouts of planned exercise/week
  • Not weight stable (+/-4.6 kg) for 3 months prior to intake
  • Unwilling to be randomized to 1 of the 3 study groups
  • Report being pregnant during the previous 6 months or planned pregnancy in the following 18 months
  • Serious medical risk such as cancer, recent cardiac event
  • Current use of antipsychotics or untreated depression
  • Adherence to specialized diet regimens (food allergy, vegetarian, macrobiotic)
  • Binge eating disorder
  • Planning to movie to a location and no longer having access to rural clinic site

Sites / Locations

  • Energy Balance Lab, The University of Kansas

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Group Phone Conference Call

Individual Phone Call

Enhanced Usual Care

Arm Description

Delivery: Group Phone Diet: PCMs

Delivery: Individual Phone Call Diet: PCMs

Delivery: Face-to-Face Diet: Conventional Diet

Outcomes

Primary Outcome Measures

Weight

Secondary Outcome Measures

Weight
Waist circumference
Triglycerides
HDL-cholesterol
Blood pressure
Fasting glucose
Cost effectiveness (process flow chart)
Cost/kg of weight loss with be assessed and compared among other published interventions.

Full Information

First Posted
September 14, 2016
Last Updated
December 10, 2019
Sponsor
University of Kansas
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT02932748
Brief Title
Midwest Diet and Exercise Trial
Acronym
M-DEx
Official Title
Weight Management in Rural Communities
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
January 2021 (Anticipated)
Study Completion Date
June 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Kansas
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to evaluate the effect of three weight management interventions (group phone conference calls, individual phone calls, and enhanced usual care) on weight across 18 months in overweight and obese adults recruited through and treated by rural primary care clinics.
Detailed Description
The rates of overweight/obesity are significantly higher among residents of rural areas compared to their urban counterparts. Recent focus to provide whole-person health care suggests that rural primary care clinics may provide an ideal setting for delivery of weight management. This study is a 3 group randomized trial to evaluate intervention delivery. The investigators will randomize 200 overweight/obese adult residents of rural towns (town population < 50,000) who obtain health care at primary care clinics to one of three groups for an 18 month trial (6 month weight loss; 12 month weight maintenance). Group 1) Group phone (GP)/Portion-Controlled Meals (PCM) Group 2) Individual phone (IP)/PCM Group 3) Enhanced usual care (EUC)/Conventional Diet (CD) All participants will receive a progressive physical activity program. Physical activity will progress from 45 min/wk in month 1 to 225 min/wk in month 4 and remain at 225 min/wk for the duration of the 18 month study for Group 1 & 2. Physical activity will progress from 45 min/wk in month 1 to 150 min/wk in month 4 and remain at 150 min/wk for the duration of the 18 month study for Group 3. Participants on the CD will be asked to consume a nutritionally balanced, reduced energy, high volume, lower fat (fat= 20-30% energy) diet recommended by the Academy of Nutrition and Dietetics and the USDA's MyPlate approach. Examples of meal plans consisting of suggested servings of proteins, grains, fruits and vegetables, dairy and fats based on individuals energy needs will be provided. Participants using PCM will consume PCMs with the addition of 5 fruits and vegetables per day during weight loss. EUC will meet with a health educator every 6 months to discuss weight management topics. GP & IP will receive the weight management intervention over the phone weekly during weight loss and biweekly during weight maintenance tracking diet and physical activity and will submit the results to a health educator prior to every meeting.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Loss, Obesity, Body Weight

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
187 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group Phone Conference Call
Arm Type
Experimental
Arm Description
Delivery: Group Phone Diet: PCMs
Arm Title
Individual Phone Call
Arm Type
Experimental
Arm Description
Delivery: Individual Phone Call Diet: PCMs
Arm Title
Enhanced Usual Care
Arm Type
Active Comparator
Arm Description
Delivery: Face-to-Face Diet: Conventional Diet
Intervention Type
Dietary Supplement
Intervention Name(s)
Portion Controlled Meals (PCM)
Intervention Description
Portion controlled meals provide conveniently packaged, low-energy, high-nutritional content food.
Intervention Type
Behavioral
Intervention Name(s)
Group Phone (GP)
Intervention Description
Weight management program delivered via group conference call.
Intervention Type
Dietary Supplement
Intervention Name(s)
Conventional Diet
Intervention Description
Conventional diet (CD) will consist of a nutritionally balanced, reduced energy, high volume, lower fat (fat= 20-30% energy) diet based on USDA's MyPlate recommendations.
Intervention Type
Behavioral
Intervention Name(s)
Individual Phone (IP)
Intervention Description
Weight management program delivered via individual phone call.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Usual Care (EUC)
Intervention Description
Weight management topics delivered face-to-face at clinic office every 6 months.
Primary Outcome Measure Information:
Title
Weight
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Weight
Time Frame
12, 18, and 24 months
Title
Waist circumference
Time Frame
6, 12, and 18 months
Title
Triglycerides
Time Frame
6, 12, and 18 months
Title
HDL-cholesterol
Time Frame
6, 12, and 18 months
Title
Blood pressure
Time Frame
6, 12, and 18 months
Title
Fasting glucose
Time Frame
6, 12, and 18 months
Title
Cost effectiveness (process flow chart)
Description
Cost/kg of weight loss with be assessed and compared among other published interventions.
Time Frame
6 and 18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Body mass index 25 to 45 kg/m2 Clearance from primary care physician Exclusion Criteria: Unable to participate in moderate intensity physical activity Participation in weight loss or physical activity program in previous 6 months Greater than 3, 30-min bouts of planned exercise/week Not weight stable (+/-4.6 kg) for 3 months prior to intake Unwilling to be randomized to 1 of the 3 study groups Report being pregnant during the previous 6 months or planned pregnancy in the following 18 months Serious medical risk such as cancer, recent cardiac event Current use of antipsychotics or untreated depression Adherence to specialized diet regimens (food allergy, vegetarian, macrobiotic) Binge eating disorder Planning to movie to a location and no longer having access to rural clinic site
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joseph Donnelly, EdD
Organizational Affiliation
University of Kansas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Energy Balance Lab, The University of Kansas
City
Lawrence
State/Province
Kansas
ZIP/Postal Code
66045
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
29454140
Citation
Gorczyca AM, Washburn RA, Ptomey L, Mayo MS, Sullivan DK, Gibson CA, Lee R, Stolte S, Donnelly JE. Weight management in rural health clinics: The Midwest diet and exercise trial. Contemp Clin Trials. 2018 Apr;67:37-46. doi: 10.1016/j.cct.2018.02.006. Epub 2018 Feb 15.
Results Reference
derived

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Midwest Diet and Exercise Trial

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