RecruitingNot ApplicableNCT07525622

Basic Carbohydrate Counting in Prediabetes

The Effect of Basic Carbohydrate Counting on HbA1c in Prediabetes: A Randomized Controlled Trial


Sponsor

Hamide Sahin

Enrollment

120 participants

Start Date

Apr 27, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Type 2 diabetes mellitus (T2DM) is a major global health problem with rapidly increasing prevalence. Prediabetes represents a high-risk state for developing T2DM and is often asymptomatic, delaying diagnosis and intervention. Early identification and effective lifestyle interventions are essential to prevent or delay the progression to diabetes. Primary care settings provide an important opportunity for screening and implementing preventive strategies. Lifestyle modification, including dietary changes and physical activity, is the cornerstone of diabetes prevention. Carbohydrate counting is a medical nutrition therapy widely used in diabetes management and has been shown to improve glycemic control. However, there is limited evidence regarding its effectiveness in individuals with prediabetes. This study aims to evaluate the effect of basic carbohydrate counting education on HbA1c levels in individuals with prediabetes in a primary care setting. This randomized controlled trial will be conducted in the Family Medicine outpatient clinic of Marmara University Hospital. Individuals aged 18 years and older with HbA1c levels between 5.7% and 6.4% will be included. Participants will be randomized into intervention and control groups in a 2:1 ratio. The control group will receive standard lifestyle recommendations, while the intervention group will receive additional structured basic carbohydrate counting education in three sessions. HbA1c levels will be measured at baseline,at third and at 6 months. Secondary outcomes include body weight, body mass index, waist circumference,lipid panel and carbohydarte counting knowledge scale The findings of this study are expected to contribute to the development of effective, scalable, and practical nutritional interventions for diabetes prevention in primary care


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Adults aged 18 years and older
  • Able to read and write Individuals with prediabetes who are not using or are unwilling to initiate oral antidiabetic drugs.

Exclusion Criteria7

  • Individuals with a diagnosis of diabetes mellitus
  • Those who have previously received carbohydrate counting training or are currently applying carbohydrate counting
  • Individuals with low daily carbohydrate intake (<100 g/day)
  • Presence of uncontrolled medical conditions that may affect dietary intake, as determined by the investigator
  • Pregnant or breastfeeding women, or those planning pregnancy during the study period
  • Participation in another clinical study Inability or unwillingness to provide informed consent or comply with study procedures
  • Cognitive impairment or communication difficulties (hearing, understanding, or speaking)

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALCarbohydrate Couinting-Based Nutrition Education

Participants assigned to the intervention group will receive a structured nutrition education program based on carbohydrate counting principles. The program will be delivered by a physician and will cover carbohydrate identification, portion estimation, meal planning, and practical application in daily dietary habits. The aim of the intervention is to improve glycemic control by increasing nutritional knowledge and promoting behavioral changes. Outcome measures will be evaluated at baseline, 3 months, and 6 months.

BEHAVIORALStandard Care (No Structured Nutrition Education)

Participants in the control group will receive standard care without structured carbohydrate counting-based nutrition education.


Locations(1)

Marmara University Hospital

Istanbul, Pendik, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07525622


Related Trials