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Completed

NCT Number: NCT05807243

Description of Immunosenescence Biomarkers and Nutritional Intervention to Evaluate the Implementation of Digital Tools

Descriptive comparative study of immunosenescence markers and their association with nutritional, metabolic, metabolomic and genetic characteristics in young (control), senior (age-associated immunosenescence), and populations susceptible to premature immunosenescence such as obese patients, cancer patients and patients who developed severe forms of COVID19 or persistent COVID19.

In one of these populations of premature immunosenescence, the population group with overweight or obesity, a prospective and cross-sectional nutritional intervention study is proposed, with data capture and monitoring using digital tools, to evaluate the evolution of immunosenescence markers and assess more objectively and effectively the nutritional status and help in making personalised decisions thanks to the application of these tools. This nutritional intervention will be focused on controlled and safe weight loss that will allow the capture of a large number of variables on lifestyle and dietary habits, nutritional assessment, biochemical, metabolic, genetic, metagenomic, lipidomic and metabolomic markers measured statically and also continuously.

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Key information

Conditions

Chronic Disease Disease Attributes Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IMDEA Food

Madrid, 28049, Spain

About this study

The study consists of data capturing to evaluate the differential pattern of molecular markers of immunosenescence in different population groups, and applying a hypocaloric diet in the obesity subgroup together with recommendations for improving lifestyle habits. The data capture of this group during the intervention will be carried out with different sensors and questionnaires for a month. To do this, they will have to follow the explanations of the researchers.

The data capture during the nutritional intervention (only for the overweight and obese population group) will be done as follows:

Group 1 (Traditional → Digital): will start with traditional data-collection methods, i.e. filling in nutritional and lifestyle questionnaires (Visit 1 to Visit 2). After two weeks, they will start capturing data digitally through the application of sensors (Visit 2 to Visit 3).

Group 2 (Digital → Traditional): will start with digital data-collection methods, using sensors and taking pictures of what they eat with a smartphone (Visit 1 to Visit 2). After two weeks, they will start capturing data traditionally, by filling in nutritional and lifestyle questionnaires (Visit 2 to Visit 3).

The nutritional intervention participant group will follow the tailored nutritional weight loss diet and lifestyle guidelines, which will be provided to them at the start of the study by the researchers. In addition, they should follow instructions for proper continuous data collection using sensors. This will avoid biases in the data collection process.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(commun for all groups):

  • Men/women
  • Minimum 18 years old
  • Adequate cultural level and understanding of the clinical study.
  • Agree to participate voluntarily in the study and give written informed consent.

Population-specific inclusion criteria:

  • Overweight/obese population:
  • BMI 25-35 Kg/m2
  • Ability to handle electronic devices for data capture.
  • Healthy young population:
  • Between 18 and 25 years old (both inclusive).
  • Senior population
  • Over 55 years of age.
  • Oncology patients
  • Over 18 years of age.
  • With a clinical diagnosis of an active tumour process.
  • Patients who developed severe or persistent COVID-19:
  • Severe COVID-19: Patients who have suffered from COVID-19 disease and whose symptomatology is considered within the clinical pictures of severity of this disease, which may include: severe pneumonia, acute respiratory distress syndrome (ARDS), presence of respiratory failure (SaO2 <90% room air) or respiratory rate ≥ 30 breaths per minute, sepsis, septic shock, thromboembolism and multi-organ dysfunction (including acute cardiac and renal injuries).
  • COVID-19 persistence: Patients who have had COVID-19 disease and who remain with active symptomatology after what is considered the acute phase of the disease, after 4 or even 12 weeks, with symptoms persisting over time.

Exclusion criteria

  • Dementia, mental illness or diminished cognitive function that can hinder the subject's participation on the study.
  • Severe diseases (liver disease, kidney disease, etc.)
  • BMI > 35 Kg/m2
  • Pregnancy or breastfeeding.

Population-specific exclusion criteria:

  • Overweight/obese population:
  • BMI <25 Kg/m2 or > 35 Kg/m2
  • Pharmacological treatment for weight loss.
  • Refusal to be monitored for one month by means of sensors and nutritional visits.
  • Refusal to follow healthy eating guidelines for weight loss.
  • Healthy young population:
  • Chronic or acute pathologies.

Treatment and study plan

Dietary intervention for healthy weight loss

Other

Balanced and varied dietary plan adjusted to each participant's needs, with an approximate reduction of 500 Kcal from their total metabolic expenditure. The diet will be followed by the subjects during the 4 weeks of the study.

Primary outcomes

  1. BMI

    Time frame: 1 month

    Only in the obese/overweight population.

    Change in body mass index (Kg/m2)

  2. Blood Glucose

    Time frame: 1 month

    Change in blood glucose (mg/dl). Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  3. Concentration of interstitial glucose

    Time frame: 15 days

    Only in the obese/overweight population.

    Change in Interstitial Glucose (mgl/dl) measured continuously with the Freestyle glucometer (Abbott Laboratories)

  4. Blood lymphocytes

    Time frame: 12 months

    Variation in the percentage of blood lymphocytes analysed by flow cytometry in five different population groups (young healthy population, elderly, overweight-obese, cancer patients, and patients who developed severe forms of COVID-19 or persistent COVID-19).

    Other variables (described in the Secondary Outcomes), such as biochemical parameters, genetical data, microbiota, etc., will also be analyzed in order to identify specific molecular markers of immunosenescence.

Secondary outcomes

  1. Weight

    Time frame: 1 month

    Weight change (Kg)

  2. WC

    Time frame: 1 month

    Change in waist circumference (cm)

  3. Body composition

    Time frame: 1 month

    Change in % of fat mass

  4. Blood pressure

    Time frame: 1 month

    During the 2 weeks in which the participant gathers the information via Traditional data-collection method, it will be measured in the study visits with an automatic Digital Blood Pressure Monitor Model M3 (OMRON HEALTHCARE UK, Kyoto, Japan).

    And during the 2 weeks in which the participant gathers the information via the Digital data-collection method, it will be measured with the Smartwatch Fitbit Sense.

  5. Heart Rate

    Time frame: 1 month

    During the 2 weeks in which the participant gathers the information via Traditional data-collection method, it will be measured in the study visits with an automatic Digital Blood Pressure Monitor Model M3 (OMRON HEALTHCARE UK, Kyoto, Japan).

    And during the 2 weeks in which the participant gathers the information via the Digital data-collection method, it will be measured with the Smartwatch Fitbit Sense.

  6. Dietary intake

    Time frame: 1 month

    Traditional data-collection method: Two 3-day dietary records (for two working days and a holiday); Digital data-collection method: Pictures of food taken with a smartphone.

  7. Physical activity

    Time frame: 1 month

    One same outcome measured during 2 weeks with one method and during the other 2 weeks with another method:

    During the 2 weeks in which the participant gathers the information via Traditional data-collection method, it will be measured via the validated International Physical Activity Questionnaire (USA Spanish version translated 3/2003 - Short last 7 DAYS self-administered version of the IPAQ - Revised August 2002).

    And during the 2 weeks in which the participant gathers the information via the Digital data-collection method, it will be measured with the Smartwatch Fitbit Sense.

  8. Sleep

    Time frame: 1 month

    One same outcome measured during 2 weeks with one method and during the other 2 weeks with another method:

    During the 2 weeks in which the participant gathers the information via Traditional data-collection method, it will be measured via the validated Oviedo Sleep Questionnaire. In the Oviedo Sleep Questionnaire, the higher the score, the greater insomnia's severity.

    And during the 2 weeks in which the participant gathers the information via the Digital data-collection method, it will be measured with the Smartwatch Fitbit Sense.

  9. Mental health state

    Time frame: 1 month

    One same outcome measured during 2 weeks with one method and during the other 2 weeks with another method:

    During the 2 weeks in which the participant gathers the information via Traditional data-collection method, it will be measured via the validated Depression Anxiety and Stress Scale - 21 (DASS-21). In the Depression Anxiety and Stress Scale, the higher the score, the greater the stress, anxiety and depression levels.

    And during the 2 weeks in which the participant gathers the information via the Digital data-collection method, it will be measured with the Smartwatch Fitbit Sense.

  10. Cognition

    Time frame: 1 month

    Measured via the validated Mini-mental state examination (MMSE). In the Mini-mental state examination, the higher the score, the better the cognitive status.

  11. Health status and quality of life

    Time frame: 1 month

    Measured via the validated Short Form-36 Health Survey (SF-36). In the Short Form-36 Health Survey, the higher the score, the better the quality of life and health status.

  12. Percentage of glycated haemoglobin

    Time frame: 1 month

    During the 2 weeks in which the participant gathers the information via Traditional data-collection method, it will be only measured in the study visits with the blood tests.

    And during the 2 weeks in which the participant gathers the information via the Digital data-collection method, it will be measured continuously with the Freestyle glucometer (Abbott Laboratories), and in the study visits with the blood tests.

  13. Total cholesterol

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  14. Low density lipoprotein (LDL)

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  15. High density lipoprotein (HDL)

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  16. Triglycerides

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  17. Apo A1

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  18. Apo B

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  19. Insulin

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  20. Glycated hemoglobin (HbA1c)

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  21. Homeostatic model assessment (HOMA)

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  22. Albumin

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  23. Prealbumin

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  24. C-reactive protein (CRP)

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  25. Leptin

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  26. Adinopectin

    Time frame: 1 month

    Blood samples are going to be collected in visit 1 and visit 3 in the obese population, and in the visit 1 in the other populations.

  27. Faecal microbiota

    Time frame: 1 month

    Faecal microbiota taxonomic profiling through shotgun sequencing.

  28. Gut dysbiosis

    Time frame: 1 month

    Lipopolysaccharide-binding protein (LBP) levels as an indirect measure of intestinal dysbiosis.

  29. Genotype

    Time frame: 1 month

    Genotyping of single nucleotide genetic variants (SNPs) and specific mutations associated with metabolism, nutrition and immunodegenerative processes.

  30. Gene expression

    Time frame: 1 month

    Expression panels in genes related to the regulation of metabolism, inflammation, immunity, oxidation, nutrition and immunodegenerative processes.

Sponsors and collaborators

Lead sponsor

IMDEA Food

Other

Registry information

Official study title

Descriptive Study of Molecular Markers of Immunosenescence With Nutritional Intervention to Evaluate the Implementation of Digital Tools in the Capture of Nutritional Data

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Apr 11, 2023
Registry last updated
Apr 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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