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Effect of Curd Cheese on Metabolic Health in Adults

27. juni 2026 opdateret af: Süleyman Kılıç

The Effect of a Diet Intervention Supplemented With Curd Cheese on Anthropometric Measurements, Glycemia, and Lipidemia in Adults Applying to Darıca Healthy Life Center

This randomized controlled trial aims to evaluate the effects of a diet supplemented with curd cheese on anthropometric measurements, glycemia, and lipid profile in overweight adults. Participants aged 40-64 years with a BMI above 25 will be randomly assigned to an intervention group receiving 100 g of curd cheese at breakfast for 8 weeks or to a control group receiving a standard healthy diet without curd cheese. Primary outcomes include changes in fasting blood glucose and HbA1c, while secondary outcomes are changes in body composition, waist circumference, and lipid profile (HDL, LDL, triglycerides, total cholesterol).

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

Metabolic disorders, including obesity, dyslipidemia, and type 2 diabetes mellitus, are major public health concerns worldwide. Dietary protein quality and source have been shown to play important roles in regulating glucose and lipid metabolism. Whey-derived proteins are rich in branched-chain amino acids and bioactive peptides that may enhance insulin sensitivity, promote satiety, and improve lipid profiles.

Curd cheese (lor cheese) is a traditional dairy product obtained during whey processing, characterized by its high-quality protein, low fat content, and rich calcium composition. It represents an affordable and accessible food that could be incorporated into dietary interventions targeting metabolic health improvement.

This study aims to investigate the effects of a curd cheese-supplemented diet on anthropometric parameters, glycemic control (including fasting glucose and HbA1c), and lipid profile (total cholesterol, HDL, LDL, and triglycerides) in adults attending the Darıca Healthy Life Center. Participants will follow a controlled dietary intervention with or without curd cheese for eight weeks.

The hypothesis of this study is that regular consumption of curd cheese as part of a balanced diet may improve metabolic parameters through increased protein intake, better glycemic regulation, and enhanced lipid metabolism.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

44

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • DARICA
      • Kocaeli, DARICA, Tyrkiet (Türkiye), 41700
        • Darıca Healthy Life Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Individuals aged 40-64 years.
  • Body Mass Index (BMI) greater than 25 kg/m².
  • Individuals who voluntarily applied to the Darıca Healthy Life Center and agreed to participate in the study.
  • Individuals who have had HbA1c, glucose, and lipid profile measurements within the past month, or will have these measurements taken as part of this study.
  • Individuals who are able to comply with the curd cheese-supplemented dietary intervention for at least 8 weeks.
  • Individuals who have signed the written informed consent form.

Exclusion Criteria:

  • Individuals diagnosed with diabetes mellitus.
  • Individuals with chronic diseases such as renal, hepatic, or cardiac failure.
  • Individuals with lactose intolerance or allergy to milk and dairy products.
  • Pregnant or lactating women.
  • Individuals with restricted protein intake for any medical reason.
  • Individuals who have participated in another dietary intervention program within the last 3 months.
  • Individuals diagnosed with psychiatric disorders requiring regular treatment.
  • Individuals with irregular lifestyles or communication difficulties that may prevent adherence to the dietary intervention.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Curd Cheese Supplemented Diet Group

Intervention Group - Arm Description:

Participants in this arm follow a customized dietary plan for 8 weeks that includes daily servings of curd cheese. The diet is balanced for energy and macronutrient distribution according to individual needs. Curd cheese, as a high-quality protein and calcium source, is included to assess its specific effects on glucose and lipid parameters. This arm is designed to evaluate the unique metabolic effects of curd cheese supplementation compared to the control group.

This intervention consists of daily consumption of 100 grams of curd cheese as part of a personalized dietary plan for 8 weeks. Curd cheese is consumed at breakfast and integrated into the participants' regular meal plans. The diet is balanced for total energy and macronutrient distribution according to individual nutritional needs. All participants in this arm receive the same type and brand of curd cheese throughout the intervention period.
Ingen indgriben: Standard Diet Group
Participants in this arm follow a standard dietary plan for 8 weeks without curd cheese. The diet is balanced according to individual energy and macronutrient needs. This arm serves as a comparison group to determine the specific effects of curd cheese supplementation observed in the intervention group.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in HbA1c Levels
Tidsramme: Baseline and after 8 weeks of intervention
To evaluate the effect of a curd cheese-supplemented diet on glycemic control by assessing changes in HbA1c levels from baseline to the end of the 8-week intervention.
Baseline and after 8 weeks of intervention

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Fasting Glucose
Tidsramme: Baseline and after 8 weeks
To assess short-term glycemic response by measuring fasting blood glucose at baseline and after the 8-week intervention.
Baseline and after 8 weeks
Change in Lipid Profile
Tidsramme: Baseline and after 8 weeks
To evaluate the effect of curd cheese supplementation on lipid metabolism by assessing changes in total cholesterol, LDL, HDL, and triglycerides from baseline to the end of the intervention.
Baseline and after 8 weeks
Change in Anthropometric Measures
Tidsramme: Baseline and after 8 weeks
To evaluate changes in body mass index (BMI) from the start to the end of the intervention.
Baseline and after 8 weeks
Change in Anthropometric Measures
Tidsramme: Baseline and after 8 weeks
To assess changes in body weight from baseline to the end of the intervention.
Baseline and after 8 weeks
Change in Anthropometric Measures
Tidsramme: Baseline and after 8 weeks
To evaluate changes in body fat percentage from the beginning to the end of the intervention.
Baseline and after 8 weeks
Change in Anthropometric Measures
Tidsramme: Baseline and after 8 weeks
To assess changes in waist circumference from the beginning to the end of the intervention.
Baseline and after 8 weeks

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Efterforskere

  • Ledende efterforsker: Ahmet M GÜNAL, PhD, RD, Halic University
  • Studieleder: Salim YILMAZ, PhD, Acıbadem Mehmet Ali Aydınlar University

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

12. december 2025

Primær færdiggørelse (Faktiske)

22. maj 2026

Studieafslutning (Faktiske)

16. juni 2026

Datoer for studieregistrering

Først indsendt

16. juni 2026

Først indsendt, der opfyldte QC-kriterier

27. juni 2026

Først opslået (Faktiske)

30. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

30. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

27. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

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INGEN

IPD-planbeskrivelse

Individual participant data (IPD) will not be shared outside the research team to ensure participant privacy and confidentiality.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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