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Not yet recruitingNCT07861516LONGEVITY-NEXTUpdated Oct 6, 2026

Non-Invasive Assessment of Early Health Determinants in Children and Adolescents

An observational study in Cardiometabolic Health Indicators and Child Health, sponsored by Fondazione Policlinico Universitario Agostino Gemelli IRCCS. Not yet recruiting at 1 site in Italy. Open to participants aged 6 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-06.

Sponsored by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Observational

Updated Oct 6, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
2,000
Ages
6 Years to 17 Years
Sex
All
01

Study summary

LONGEVITY-NEXT is a single-center, non-profit observational study designed to assess early non-invasive determinants of cardiometabolic, functional, behavioral, and environmental health in children and adolescents aged 6 to 17 years from the general population. Participants will undergo a standardized 15-20-minute non-invasive assessment including anthropometric measurements, blood pressure and heart rate, handgrip strength, dietary habits and adherence to the Mediterranean diet, physical activity, recreational screen time, sleep duration, tobacco smoke exposure, early-life factors, chronic health conditions, and family cardiometabolic history. The primary outcome is the distribution of the number of unfavorable cardiometabolic, behavioral, and environmental health domains per participant. The study involves no experimental treatment, drug, investigational medical device, invasive procedure, or modification of usual care. Optional repeated assessments may occur opportunistically during the study while participants remain between 6 and 17 years of age.

Read the detailed description

LONGEVITY-NEXT is a single-center, non-profit, non-interventional, minimal-risk pediatric observational study developed in scientific and methodological continuity with the adult Longevity Check-up program, while constituting an independent study specifically adapted to children and adolescents. The study is based primarily on a cross-sectional baseline assessment using exclusively non-invasive procedures.

Participants may be enrolled at Fondazione Policlinico Universitario Agostino Gemelli IRCCS or during health-promotion, community, school, or Longevity-related initiatives organized, authorized, or coordinated by the Sponsor. These territorial activities are operational settings of the same single-center study and do not constitute independent study sites.

The assessment includes anthropometric measurements, blood pressure and heart rate, handgrip strength, adherence to the Mediterranean diet using the KIDMED questionnaire, reported frequency of processed or ultra-processed food intake, physical activity, recreational screen time, habitual sleep duration, tobacco smoke exposure, early-life factors, chronic health conditions, and family cardiometabolic history.

Optional observational reassessments may occur during subsequent LONGEVITY-NEXT initiatives. These reassessments are voluntary, opportunistic, and are not scheduled at predefined intervals. No reassessment will be performed after the participant reaches 18 years of age. No experimental treatment, investigational medical device, invasive procedure, or modification of usual clinical care is involved. Exploratory analyses will assess associations among the individually registered cardiometabolic, functional, behavioral, environmental, early-life, and family measures using statistical methods appropriate to the nature of the variables. Where specifically authorized pseudonymized parent-child linkage is available, exploratory analyses will also assess relationships between the child's profile and corresponding or complementary measures available for participating parent(s).

02

Conditions studied

  • Cardiometabolic Health Indicators
  • Child Health

Keywords

  • Pediatric Health
  • Cardiometabolic Health
  • Life-Course Health
  • Mediterranean Diet
  • Physical Activity
  • Sedentary Behavior
  • Screen Time
  • Sleep Duration
  • Tobacco Smoke Exposure
  • Handgrip Strength
  • Health Promotion
03

In context

Motor Activity

2,431 studies on the registry are indexed under Motor Activity; 1,162 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 100 across 292 observational studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS is the lead sponsor of 920 studies on the registry; 529 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Children and adolescents aged 6 to 17 years from the general population who voluntarily participate in LONGEVITY-NEXT and meet the protocol-defined eligibility criteria. Participants may be enrolled at Fondazione Policlinico Universitario Agostino Gemelli IRCCS or during health-promotion, community, school, or other territorial initiatives organized, authorized, or coordinated by the Sponsor. The presence of chronic conditions or functional limitations does not in itself preclude participation, provided that study participation is considered appropriate.

Inclusion criteria

  • Age 6 to 17 years at the time of assessment.
  • Written informed consent for study participation and personal data processing provided by both parents exercising parental responsibility or, when applicable, by the legally appointed guardian, according to applicable regulations and Ethics Committee-approved procedures.
  • Assent of the minor obtained using age- and maturity-appropriate procedures and documentation.
  • Willingness of the child/adolescent and family to participate in the non-invasive assessment, even if individual measurements, tests, or information cannot be obtained.

Exclusion criteria

Exclusion Criteria:

  • Age younger than 6 years or older than 17 years at the time of assessment.
  • Failure to obtain the required written informed consent for study participation and personal data processing from both parents exercising parental responsibility, where applicable, or from the legally appointed guardian.
  • Failure to obtain the minor's assent using age- and maturity-appropriate procedures.
  • Explicit objection by the minor to study participation or continuation of the assessment.
  • Acute clinical conditions, illness, significant discomfort, or other circumstances that, in the investigator's judgment, make participation temporarily inappropriate.
  • Refusal of the personal data processing required for study participation.
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Children and Adolescents Aged 6-17 Years

    Children and adolescents aged 6 to 17 years from the general population who voluntarily participate in LONGEVITY-NEXT and undergo the non-invasive multidimensional assessment specified in the study protocol.

06

What researchers measure

Primary outcomes

  1. Number of Unfavorable Cardiometabolic, Behavioral, and Environmental Health Domains per Participant

    For each participant, a count will be calculated across seven protocol-defined domains: weight status, blood pressure, adherence to the Mediterranean diet, physical activity, recreational screen time, sleep duration, and tobacco smoke exposure. Each domain classified as unfavorable contributes one point. The total count ranges from 0 to 7, with higher values indicating a greater number of unfavorable domains.

    Time frame: Baseline

Secondary outcomes

  1. Body Weight

    Body weight will be measured in kilograms using a calibrated scale.

    Time frame: Baseline

  2. Waist Circumference

    Waist circumference will be measured in centimeters using a flexible non-stretchable tape at the midpoint between the lower margin of the last palpable rib and the iliac crest.

    Time frame: Baseline

  3. Calf Circumference

    Calf circumference will be measured in centimeters at the maximum circumference of the dominant leg.

    Time frame: Baseline

  4. Systolic Blood Pressure

    Systolic blood pressure will be measured in mmHg using a device validated for pediatric use and an appropriately sized cuff.

    Time frame: Baseline

  5. Right-Hand Handgrip Strength

    Right-hand handgrip strength will be measured in kilograms using an adjustable dynamometer suitable for pediatric use. The best value obtained from two trials will be recorded.

    Time frame: Baseline

  6. KIDMED Score

    Adherence to the Mediterranean diet will be assessed using the KIDMED questionnaire. The total KIDMED score will be calculated according to the original scoring system, with higher scores indicating greater adherence to the Mediterranean diet.

    Time frame: Baseline

  7. Days With at Least 60 Minutes of Moderate-to-Vigorous Physical Activity

    Physical activity will be assessed as the number of days during the previous 7 days in which the participant accumulated at least 60 minutes of moderate-to-vigorous physical activity.

    Time frame: Baseline

  8. Recreational Screen Time on School Days

    Recreational screen time on school days will be assessed in hours per day, including television, video or streaming, videogames, smartphones, tablets, and computers used for non-school purposes.

    Time frame: Baseline

  9. Habitual Sleep Duration on School Days

    Habitual nocturnal sleep duration on school days will be estimated from reported sleep onset and wake times and expressed in hours per night.

    Time frame: Baseline

  10. Passive Tobacco Smoke Exposure Status

    Passive tobacco smoke exposure will be assessed using protocol-defined structured questions administered to the parent/legal guardian and, when appropriate, to the participant. Exposure will be recorded as present or absent based on reported exposure at home, in vehicles, and/or other indoor environments.

    Time frame: Baseline

  11. Birth Weight

    Birth weight will be recorded, when known, as reported by the parent or legal guardian.

    Time frame: Baseline

  12. Reported Chronic Health Conditions

    Physician-diagnosed chronic conditions will be assessed by structured parent/legal guardian interview using protocol-defined categories. Diagnoses are reported by the parent/legal guardian and are not independently verified through clinical documentation.

    Time frame: Baseline

  13. Proportion of Participants With Waist-to-Height Ratio ≥0.50

    The proportion of participants with a waist-to-height ratio ≥0.50 will be calculated.

    Time frame: Baseline

  14. Change From Baseline in the Number of Unfavorable Health Domains

    Among participants with at least one optional reassessment, the change from baseline in the total number of unfavorable protocol-defined health domains will be calculated. The total count is based on seven domains: weight status, blood pressure, adherence to the Mediterranean diet, physical activity, recreational screen time, sleep duration, and tobacco smoke exposure. Negative values indicate fewer unfavorable domains and positive values indicate more unfavorable domains compared with baseline.

    Time frame: Baseline and each optional reassessment through study completion, up to 10 years

  15. Number of Unfavorable Health Domains at Optional Reassessment

    Among participants undergoing an optional reassessment, the total number of unfavorable protocol-defined health domains will be calculated using the same seven domains assessed at baseline: weight status, blood pressure, adherence to the Mediterranean diet, physical activity, recreational screen time, sleep duration, and tobacco smoke exposure. The total score ranges from 0 to 7, with higher values indicating a greater number of unfavorable health domains.

    Time frame: Each optional reassessment after baseline through study completion, up to 10 years

  16. Height

    Height will be measured in centimeters using a standard stadiometer.

    Time frame: Baseline

  17. Body Mass Index

    Body mass index (BMI) will be calculated as body weight in kilograms divided by height in meters squared and expressed as kg/m².

    Time frame: Baseline

  18. BMI-for-Age Z-Score

    BMI-for-age z-score will be calculated using age- and sex-specific World Health Organization pediatric reference data.

    Time frame: Baseline

  19. Pediatric Weight Status Category

    Weight status will be classified according to World Health Organization BMI-for-age criteria as severe thinness, thinness, normal weight, overweight, or obesity.

    Time frame: Baseline

  20. Waist-to-Height Ratio

    Waist-to-height ratio will be calculated as waist circumference in centimeters divided by height in centimeters and expressed as a dimensionless ratio.

    Time frame: Baseline

  21. Mid-Upper Arm Circumference

    Mid-upper arm circumference will be measured in centimeters at the midpoint between the acromion and olecranon of the non-dominant arm.

    Time frame: Baseline

  22. Triceps Skinfold Thickness

    Triceps skinfold thickness will be measured in millimeters using a calibrated skinfold caliper on the non-dominant arm.

    Time frame: Baseline

  23. Diastolic Blood Pressure

    Diastolic blood pressure will be measured in mmHg using a device validated for pediatric use and an appropriately sized cuff.

    Time frame: Baseline

  24. Pediatric Blood Pressure Category

    Blood pressure will be classified according to pediatric reference criteria based on age, sex, and height.

    Time frame: Baseline

  25. Left-Hand Handgrip Strength

    Left-hand handgrip strength will be measured in kilograms using an adjustable dynamometer suitable for pediatric use. The best value obtained from two trials will be recorded.

    Time frame: Baseline

  26. KIDMED Adherence Category

    Participants will be classified according to the KIDMED score as having low adherence (score ≤3), intermediate adherence (score 4-7), or high adherence (score ≥8) to the Mediterranean diet.

    Time frame: Baseline

  27. Reported Frequency of Processed or Ultra-Processed Food Intake

    Reported frequency of processed or ultra-processed food intake will be assessed using protocol-defined structured frequency questions administered to the parent/legal guardian and/or the participant, as appropriate for age and maturity. Responses will be described according to the categories specified in the study data collection form.

    Time frame: Baseline

  28. Physical Activity Category

    Participants will be classified according to the number of days during the previous 7 days with at least 60 minutes of moderate-to-vigorous physical activity as favorable (7 days/week), intermediate (5-6 days/week), or unfavorable (0-4 days/week).

    Time frame: Baseline

  29. Recreational Screen Time on Weekends

    Recreational screen time on weekends will be assessed in hours per day, including television, video or streaming, videogames, smartphones, tablets, and computers used for non-school purposes.

    Time frame: Baseline

  30. Weekly Average Recreational Screen Time

    Weekly average recreational screen time will be calculated as \[(school-day screen time × 5) + (weekend screen time × 2)\] / 7 and expressed in hours per day.

    Time frame: Baseline

  31. Recreational Screen Time Category

    Participants will be classified according to weekly average recreational screen time as favorable (≤2 hours/day), intermediate (\>2 to ≤4 hours/day), or unfavorable (\>4 hours/day).

    Time frame: Baseline

  32. Habitual Sleep Duration on Weekends

    Habitual nocturnal sleep duration on weekends will be estimated from reported sleep onset and wake times and expressed in hours per night.

    Time frame: Baseline

  33. Sleep Duration Category

    Participants will be classified according to age-specific protocol-defined sleep duration categories as favorable, intermediate, or unfavorable.

    Time frame: Baseline

  34. Prematurity Status

    Prematurity will be recorded as reported by the parent or legal guardian and classified as yes, no, or unknown.

    Time frame: Baseline

  35. Gestational Age at Birth

    Gestational age at birth will be recorded in completed weeks, when known, as reported by the parent or legal guardian.

    Time frame: Baseline

  36. Family History of Diabetes Mellitus

    Reported family history of diabetes mellitus will be assessed by structured parent or legal guardian interview and recorded as present or absent.

    Time frame: Baseline

  37. Family History of Obesity

    Reported family history of obesity will be assessed by structured parent or legal guardian interview and recorded as present or absent.

    Time frame: Baseline

  38. Family History of Hypercholesterolemia

    Reported family history of hypercholesterolemia will be assessed by structured parent or legal guardian interview and recorded as present or absent.

    Time frame: Baseline

  39. Family History of Premature Myocardial Infarction

    Reported family history of premature myocardial infarction will be assessed by structured parent or legal guardian interview and recorded as present or absent. Premature myocardial infarction is defined as an event occurring before age 55 years in male relatives or before age 65 years in female relatives.

    Time frame: Baseline

  40. Family History of Stroke

    Reported family history of stroke will be assessed by structured parent or legal guardian interview and recorded as present or absent.

    Time frame: Baseline

  41. Family History of Other Cardiovascular Disease

    Reported family history of other cardiovascular disease will be assessed by structured parent or legal guardian interview and recorded as present or absent.

    Time frame: Baseline

  42. Frequency of Passive Tobacco Smoke Exposure

    Among participants with reported passive tobacco smoke exposure, the frequency of exposure will be assessed using protocol-defined structured questions and described according to the categories recorded in the study data collection form.

    Time frame: Baseline

  43. Active Smoking Status

    When appropriate according to the participant's age and maturity, current active smoking status will be assessed using protocol-defined structured questions and recorded as reported active smoking present or absent.

    Time frame: Baseline

  44. Frequency of Active Smoking

    Among participants reporting active smoking, and when appropriate according to age and maturity, the reported frequency of active smoking will be recorded using protocol-defined structured questions.

    Time frame: Baseline

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 6, 2026
Show all 1 update
  1. Oct 6, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07861516
Lead sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Responsible party
Sponsor
First posted
Oct 6, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Oct 1, 2036 (estimated)
Completion
Oct 1, 2036 (estimated)
Last update
Oct 6, 2026

Study contacts

Francesco Landi, MD, PhD
Contact
francesco.landi@policlinicogemelli.it
+39 06 30154859
Francesco Landi, MD, PhD
principal investigator · Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Federica Mammarella, MD, PhD
study director · Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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