Comparing High and Normal Protein Diets for the Dietary Remission of Type 2 Diabetes

Sponsor
University of Alabama at Birmingham (Other)
Overall Status
Completed
CT.gov ID
NCT03832933
Collaborator
(none)
117
2
2
33.7
58.5
1.7

Study Details

Study Description

Brief Summary

The purpose of this study is to examine the impact of high protein (HP) vs. normal protein (NP) diets on weight loss, loss of fat free mass (FFM), and remission of type 2 diabetes (T2D) in individuals with T2D. Both diet groups will receive dietary and physical activity guidance through a group-based weight loss program, State of Slim (SOS). The central hypothesis is that the HP diet (with ≥4 weekly servings of lean beef) will lead to greater remission of T2D vs. a NP diet by 1) producing greater weight loss and limiting weight regain and 2) preferentially reducing fat mass while preserving FFM.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: High Protein Diet
  • Behavioral: Standard Protein Diet
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
117 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparing High and Normal Protein Diets for the Dietary Remission of Type 2 Diabetes
Actual Study Start Date :
Jul 1, 2019
Actual Primary Completion Date :
Apr 22, 2022
Actual Study Completion Date :
Apr 22, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: High Protein Diet

Behavioral: High Protein Diet
16 week weight loss and 36 weight loss maintenance intervention. Approximate macronutrient distributions (carbohydrate:protein:fat) will be 32%:40%:28%.

Active Comparator: Standard Protein Diet

Behavioral: Standard Protein Diet
16 week weight loss and 36 weight loss maintenance intervention. Approximate macronutrient distributions (carbohydrate:protein:fat) will be 53%:21%:25%.

Outcome Measures

Primary Outcome Measures

  1. Change in body weight by weight scale [Baseline to 16 weeks]

    Participant body weights will be measured on a kg scale

  2. Change in body weight by weight scale [Baseline to 52 weeks]

    Participant body weights will be measured on a kg scale

Secondary Outcome Measures

  1. Change in T2D diagnosis criteria [Baseline to 52 weeks.]

    T2D diagnosis will be determined according to American Diabetes Association criteria, which includes fasting glucose <126 mg/dL or hemoglobin A1c <6.5%.

  2. Change in % body fat [Baseline to 16 weeks]

    Participant body fat will be measured by dual x-ray absorptiometry (DXA), which is the gold standard for measuring body composition.

  3. Change in % body fat [Baseline to 52 weeks.]

    Participant body fat will be measured by dual x-ray absorptiometry (DXA), which is the gold standard for measuring body composition.

  4. Change in % fat free mass (FFM) [Baseline to 16 weeks.]

    Participant FFM will be measured by dual x-ray absorptiometry (DXA), which is the gold standard for measuring body composition.

  5. Change in % FFM [Baseline to 52 weeks.]

    Participant FFM will be measured by dual x-ray absorptiometry (DXA), which is the gold standard for measuring body composition.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female

  • Age ≥18 years

  • T2D diagnosis within previous 6 years (documented physician diagnosis, use of antidiabetic medication, fasting glucose ≥126 mg/dl, and/or HbA1c ≥6.5%)

  • BMI of ≥27 kg/m2

  • Weight stable (±3kg in the last 3 months)

  • Participants using GLP-1 agonists or SLGT-inhibitors must be on a stable (≥3 months) medication dosage and not be planning to change medication dosage

  • Willing and able to participate in a weekly group class for the first 16 weeks of the study, bi-weekly classes for the remainder of the study, and willing to participate in 4 study visits over the 52 week study period.

Exclusion Criteria:
  • HbA1c concentration of ≥12%.

  • Pregnant or lactating within the past 6 months or trying to become pregnant.

  • Individuals following a vegetarian/vegan only diet

  • Food allergies (to red meats or other common protein sources)

  • Using exogenous insulin for T2D management

  • Taking other medications that could cause weight loss or weight gain (such as steroids, tricyclic antidepressants, chemotherapy, antipsychotics, prescribed or OTC weight loss agents). Oral contraceptives can be used as long as subject agrees to not change use of these during the study. Vitamins and minerals that do not have a weight effect are allowed as long as use is continued without change during the study.

  • Current alcohol or drug abuse or dependence (Subjects who have quit smoking in the last 6 months will be excluded. Smokers whose smoking habits have been stable for the last 6 months and which remain stable during the study can be included).

  • Current Eating disorder (anorexia or bulimia)

  • Any medical condition for which following a high protein diet and/or 70 minutes of exercise daily would be inadvisable.

  • Untreated or unstable hypothyroidism. Thyroid medications must be stable for at least 3 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Alabama at Birmingham Birmingham Alabama United States 35294
2 University of Colorado Anschutz Medical Campus Aurora Colorado United States 80045

Sponsors and Collaborators

  • University of Alabama at Birmingham

Investigators

  • Principal Investigator: James Hill, PhD, University of Alabama at Birmingham

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
James O. Hill, Primary Investigator, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:
NCT03832933
Other Study ID Numbers:
  • IRB-300002928
First Posted:
Feb 6, 2019
Last Update Posted:
May 10, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by James O. Hill, Primary Investigator, University of Alabama at Birmingham
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 10, 2022