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NCT06422429 | NOT YET RECRUITING | Metabolism and Nutrition Disorder


Study on the Regulatory Effects of Personalized Innovative Youtiao Intervention on Nutritional Health
Sponsor:

Y u Zhang

Information provided by (Responsible Party):

Y u Zhang

Brief Summary:

The goal of this clinical trial is to investigate the effects of personalized innovative fritters on the nutritional health of overweight and obese individuals aged 40 to 70 years. The main questions it aims to answer are: * How does consuming personalized innovative fritters affect the nutritional health of overweight and obese individuals? * What is the mechanism underlying the impact of personalized innovative oil bars on nutritional health? Participants will be randomly assigned to one of two groups: a trial group consuming personalized innovative fritters and a control group consuming traditional fritters with equal energy content. Over the course of 6 months, participants will undergo two phases of intervention separated by a two-month washout period. During the intervention, participants will be assessed comprehensively for sensory ratings and nutritional health status through biological indicators, physical examinations, and other relevant measures. Researchers will compare the trial group to the control group to determine if personalized innovative fritters lead to improvements in nutritional health compared to traditional fritters.

Condition or disease

Metabolism and Nutrition Disorder

Intervention/treatment

Traditional deep-fried Youtiao

PI Youtiao

Phase

PHASE2

Detailed Description:

Participants entered the trial with a 1-week equilibration period during which baked and fried foods were prohibited. The test group will consume personalised innovative Youtiao and the control group will uniformly consume traditional Youtiao of equal energy, 45 g 4 times per week for 8 weeks, during which time we will periodically measure biological indicators and collect biological samples to gain insight into the effects of the personalised innovative Youtiao on the participants. After completion of the 8-week intervention, a washout phase is entered. During this phase, participants will no longer ingest the Youtiao to see how they trend after stopping the intervention. Participants then enter the second phase of the trial, where the intervention process described above is continued with appropriate consumption adjustments based on the initial results of the first phase of the intervention.

Study Type : INTERVENTIONAL
Estimated Enrollment : 150 participants
Masking : QUADRUPLE
Primary Purpose : TREATMENT
Official Title : Study on the Regulatory Effects of Personalized Innovative Youtiao Intervention on Nutritional Health
Actual Study Start Date : 2025-03-01
Estimated Primary Completion Date : 2025-09-01
Estimated Study Completion Date : 2025-12-01

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 40 Years to 70 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Age between 40-70 years old (women need to be menopausal);
  • * BMI\>24 kg/m2;
  • * Consumption of fritters more than once a week.
Exclusion Criteria
  • * history of diabetes mellitus, cardiovascular disease, dyslipidaemia, renal disease, -
  • * liver disease or cancer;
  • * surgical treatment within 3 months;
  • * allergy/intolerance to the study food or any of its ingredients;
  • * breastfeeding or pregnancy;
  • * \>10% weight loss in the past 6 months;
  • * smoking or alcohol abuse;
  • * participation in another clinical study within the past 6 months

Study on the Regulatory Effects of Personalized Innovative Youtiao Intervention on Nutritional Health

Location Details

NCT06422429


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