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临床试验/NCT07416396
NCT07416396进行中(未招募)1 期

Effects of Morning and Evening Specific Compound Food Supplements on Changes in Biomarkers Associated With Longevity

University of Primorska1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年3月7日最近更新:
干预措施

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
60
试验地点
1
主要终点
Creatinine

研究概览

简要总结

The use of food supplements with the aim of increasing longevity in the general population is rapidly increasing, while high-quality clinical evidence on the efficacy of comprehensive formulations and their impact on biomarkers of aging is lacking. The present clinical trial will evaluate the effects of selected morning- and evening-speciffic dietary supplement on longevity biomarkers in a selected population of healthy adults of both sexes between the ages of 50 and 70 and compare it to placebo. The main questions it answers are: Does the 6-month use of the longevity supplement impact the 6-months change in different markers for measuring biological age compared to placebo? The study will involve 60 subjects, of whom 30 will consume the morning- and evening-speciffic longevity food supplements and 30 will consume a placebo. The study will last 6 months. The subjects will will visit the Faculty four times: at the beginning of the study (background measurement), after one, three and six months of consuming the dietary supplement or placebo. At each visit, subjects will undergo anthropometric measurements, blood pressure measurements, and blood samples will be taken to determine baseline haematocrite, albumin, creatinine, alcaline phosphatase, lipid profile, glucose concentration, inflammatory parameters, antioxidant potential, liver enzymes, and expression of genes for autophagy and oxidative stress. Subjects will also complete 3-day food diaries and questionnaires on general health, physical activity, and quality of sleep and life.

On baseline and final (six months) measurements resting metabolic rate and DXA body composition measurements will be performed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
50 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Body mass index (BMI) between 22 kg/m2 and 30 kg/m2
  • Postmenopausal women (at least 12 months without menstruation)
  • Healthy individuals, without risk of chronic non-communicable diseases
  • Signed written informed consent

排除标准

  • Acute and chronic diseases (cardiovascular diseases, diabetes, neurodegenerative diseases, gastrointestinal diseases).
  • Patients with serious clinical conditions such as cancer, severe infections, severe psychiatric disorders, autoimmune diseases, inflammatory diseases.
  • BMI less than 22 kg/m2 and greater than 30 kg/m
  • Celiac disease or gluten intolerance.
  • Presence of implants, devices or other foreign materials in the measurement area.
  • Atypical sleep patterns.
  • Use of dietary supplements and medications.
  • Extreme physical activity.
  • Excessive alcohol consumption (more than one drink per day for women, more than two drinks per day for men).

研究组 & 干预措施

Morning- and evening-speciffic longevity food supplement

Experimental

6-month daily consumption of 1 morning-specific capsule and 1 evening-specific capsule.

干预措施: Morning- and evening-specific compound food supplement (Dietary Supplement)

Control

Placebo Comparator

6-month daily consumption of 2 capsules of maltodextrin.

干预措施: Control (Dietary Supplement)

结局指标

主要结局

Creatinine

时间窗: From enrolment to the end of last measurement at 6 months.

Creatinine levels will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

Albumin

时间窗: From enrolment to the end of last measurement at 6 months.

Albumin levels will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

Glucose

时间窗: From enrolment to the end of last measurement at 6 months.

Glucose levels will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

CRP

时间窗: From enrolment to the end of last measurement at 6 months.

CRP levels will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

Lymphocyte percent

时间窗: From enrolment to the end of last measurement at 6 months.

Lymphocyte percent will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

Mean cell volume

时间窗: From enrolment to the end of last measurement at 6 months.

Mean cell volume will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

Red cell distribution width

时间窗: From enrolment to the end of last measurement at 6 months.

Red cell distribution width will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

Alcaline phosphatase

时间窗: From enrolment to the end of last measurement at 6 months.

Alcaline phosphatase will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

White blood cell count

时间窗: From enrolment to the end of last measurement at 6 months.

White blood cell count will be measured from venous blood at baseline, after 1, 3 and 6 months of daily dietary supplements use.

PhenoAge

时间窗: From enrolment to the end of last measurement at 6 months.

PhenoAge will be calculated from albumin, creatinine, glucose, lymphocyte percent, mean cell volume, red cell distribution width, alcaline phosphatase, white blood cell count and cronological age at baseline, after 1, 3 and 6 months of daily dietary supplements use.

次要结局

  • Total cholesterol(From enrolment to the end of last measurement at 6 months.)
  • LDL cholesterol(From enrolment to the end of last measurement at 6 months.)
  • HDL cholesterol(From enrolment to the end of last measurement at 6 months.)
  • Triacylglycerols(From enrolment to the end of last measurement at 6 months.)
  • Antioxidative potential(From enrolment to the end of last measurement at 6 months.)
  • Alanine aminotransferase (ALT)(From enrolment to the end of last measurement at 6 months.)
  • Aspartate aminotransferase (AST)(From enrolment to the end of last measurement at 6 months.)
  • Interleukine-6 (IL-6)(From enrolment to the end of last measurement at 6 months.)
  • Tumor necrosis factor alpha (TNF-alpha)(From enrolment to the end of last measurement at 6 months.)
  • NAD+/NADH(From enrolment to the end of last measurement at 6 months.)
  • Sleep quality(From enrolment to the end of last measurement at 6 months.)
  • World Health Organization-FIve Well-Being Index(From enrolment to the end of last measurement at 6 months.)
  • BMAL1 gene expression(From enrolment to the end of last measurement at 6 months.)
  • ATG1 gene expression(From enrolment to the end of last measurement at 6 months.)
  • SD1 gene expression(From enrolment to the end of last measurement at 6 months.)
  • mTOR gene expression(From enrolment to the end of last measurement at 6 months.)
  • SIRT1 gene expression(From enrolment to the end of last measurement at 6 months.)
  • Glutation reductase gene expression(From enrolment to the end of last measurement at 6 months.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nina Mohorko

Associate Professor

University of Primorska

研究点 (1)

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