- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03258918
A Low-Carbohydrate Diabetes Prevention Program
A Mixed Methods Pilot Study of a Low-Carbohydrate Diabetes Prevention Program Among Individuals With Prediabetes
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
An estimated 86 million US adults are have prediabetes, and, without intervention, many will develop T2DM over time. Fortunately, T2DM can be prevented or delayed through modest lifestyle changes. The landmark Diabetes Prevention Program (DPP) Trial demonstrated a 58 percent reduction in the 3-year incidence of T2DM among individuals with prediabetes who achieved 7 percent body weight loss and engaged in routine physical activity. Accordingly, the DPP lifestyle intervention has been translated to communities across the United States, and, on average, participant weight change is 4 percent at 12 months. Thus, while group-based DPPs and can effectively promote weight loss among some participants, many DPP participants do not achieve the program goal of 5 to 7 percent body weight loss.
Novel strategies to help participants achieve DPP weight-loss goals are important for two key reasons. First, weight loss is the primary driver of T2DM risk reduction, and the potential population health impact of the intervention is diminished when participants do not lose weight. Second, a growing number of health plans including Medicare offer coverage for the DPP and proposed reimbursement is largely tied to weight loss of at least 5 percent at 6 months and 12 months. The DPP costs approximately $400-$500 per participant per year. Unfortunately, organizations that offer the DPP may be reimbursed for much less than this if participants do not meet weight loss goals, which could significantly compromise the program's long-term financial sustainability.
One promising approach to help DPP participants lose more weight may be through a low-carbohydrate (LC) dietary intervention. Consistent with United States Dietary Guidelines (USDG), the original DPP Trial and translational group-based curricula recommend a low-fat (LF), calorie-restricted diet. However, there is growing controversy regarding the scientific merit of the Dietary Guidelines as well as growing recognition that LC diets may be more effective than LF diets for short-term weight loss and long-term weight maintenance. Notably, weight loss occurs without calorie restriction and LC diets improve blood glucose levels among individuals with T2DM and insulin resistance. Thus, a LC dietary intervention for prediabetes may augment individual weight loss and T2DM risk reduction while also maximizing third-party reimbursement.
The aim of this mixed methods pilot study is to test whether a LC-DPP may lead to greater weight loss than the original DPP. In addition to objective measures of this program's preliminary efficacy (e.g. weight, HbA1c) the study team will also obtain qualitative participant feedback on the intervention. Taken together, these data will be used to improve the curriculum and inform a larger-scale intervention.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Michigan
-
Ann Arbor, Michigan, Förenta staterna, 48109
- Michigan Medicine
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion criteria:
- Overweight, defined as BMI≥25 kg/m2 [31]
- HbA1c between 5.7-6.4% drawn within 6 months of the study start date
- Willingness to participate in group-based classes
- Able to engage in at least light physical activities such as walking.
Exclusion criteria:
- History of type 1 diabetes or type 2 diabetes
- Current participation in another lifestyle or behavior change program or research study
- Vegetarian or vegan lifestyle
- History of bariatric surgery
- Inability to read, write, or speak English
- Inability to provide informed consent
- Women who are pregnant or intend to become pregnant during the intervention period.
- Insured by Premier Care or Grad Care; these individuals have the opportunity to participate in a standard DPP, which is offered as a covered benefit through their health plan.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Low-Carbohydrate Diabetes Prevention Program
At least 20 individuals with prediabetes will participate in a year-long , group-based program.
|
LC-DPP participants will be instructed to follow ad-libitum very low-carbohydrate, ketogenic diet, which restricts carbohydrate intake (not including fiber) to 20-35 grams per day with the goal of achieving nutritional ketosis.
Participants will be encouraged to eat a normal amount of protein (roughly 80-120 grams per day) and to derive the remaining calories from fat.
Allowable foods include: meats, fish, poultry, eggs, cheese, seeds, nuts, leafy greens, non-starchy vegetables, and some fruits.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Change in body weight per participant over the study period
Tidsram: Baseline, 12 months
|
Measured as percent body weight loss per participant
|
Baseline, 12 months
|
|
Percentage of participants who achieve weight loss goal
Tidsram: Baseline,12 months
|
Measured as percentange of participants who achieve 5% total body weight loss
|
Baseline,12 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Change in self-reported weekly physical activity minutes
Tidsram: Baseline, 12 months
|
Participants will maintain a log of weekly physical activity minutes
|
Baseline, 12 months
|
|
Change in physical activity measured using the International Physical Activity Questionnaire
Tidsram: Baseline, 12 months
|
Participants will complete this validated survey
|
Baseline, 12 months
|
|
Change in food cravings measured using the Control of Eating Questionnaire
Tidsram: Baseline, 12 months
|
Participants will complete this validated survey
|
Baseline, 12 months
|
|
Change in stress eating measured using the Palatable Eating Motives Scale
Tidsram: Baseline, 12 months
|
Participants will complete this validated survey
|
Baseline, 12 months
|
|
Change in self-reported health measured using the Global Health PROMIS Questionnaire
Tidsram: Baseline, 12 months
|
Participants will complete this validated survey
|
Baseline, 12 months
|
|
Change in autonomous motivation measured using the Treatment Self-Regulation Questionnaire
Tidsram: Baseline, 12 months
|
Participants will complete this validated survey
|
Baseline, 12 months
|
|
Change in hemoglobin A1c
Tidsram: Baseline, 12 months
|
Measured using a laboratory blood draw
|
Baseline, 12 months
|
|
Session attendance
Tidsram: Baseline, 12 months
|
Measured as the number of sessions attended per participant
|
Baseline, 12 months
|
|
Study attrition
Tidsram: Baseline, 12 months
|
Number of participants lost to follow-up
|
Baseline, 12 months
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Change in diet as assessed by qualitative review of foods logs
Tidsram: Baseline, 12 months
|
Participants will maintain weekly food logs
|
Baseline, 12 months
|
|
Change in diet as assessed by response to survey questions
Tidsram: Baseline, 12 months
|
Participants will respond to exploratory survey questions about diet created by the study team.
|
Baseline, 12 months
|
|
Change in physical symptoms
Tidsram: Baseline, 12 months
|
Participants will respond to exploratory survey questions about physical symptoms created by the study team.
|
Baseline, 12 months
|
Samarbetspartners och utredare
Sponsor
Samarbetspartners
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- F046400
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
Kliniska prövningar på Low-Carbohydrate Diabetes Prevention Program
-
San Diego State UniversityFamily Health Centers of San DiegoAktiv, inte rekryterandeSARS-CoV-2-infektionFörenta staterna
-
Johns Hopkins UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)AvslutadHyperglykemi | Fetma | Övervikt | Viktminskning | Prediabetes | Prediabetiskt tillstånd | Nedsatt glukostolerans | Glukos, högt blod | Livsstil, hälsosam | Livsstilsriskminskning | Livsstil, stillasittandeFörenta staterna
-
Villa Garda HospitalAvslutad
-
Johns Hopkins UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)AvslutadPrediabetes | Diabetes typ 2 | Fetma, barndom | Övervikt och fetma | Livsstil, hälsosam | Övervikt, barndomFörenta staterna
-
University of Wisconsin, MadisonWisconsin Department of Health and Family Services; Kenosha County Aging...AvslutadAccidental Falls
-
University of ArizonaAvslutad
-
The University of Texas Medical Branch, GalvestonIndragenHypertoni | Prediabetiskt tillstånd | Övervikt eller fetma | Gestational viktökning
-
Universiti Sultan Zainal AbidinOkändÖvervikt och fetma | Pre-diabetesMalaysia
-
Aydin Adnan Menderes UniversityThe Scientific and Technological Research Council of TurkeyRekryteringSjälvmordstankar | Förebyggande av självmord | SkolvägledningTurkiet (Türkiye)
-
University of North Carolina, Chapel HillAmerican Diabetes AssociationRekryteringFetma | Typ 2-diabetes mellitus | Hetsätningsstörning | HetsätningFörenta staterna