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Biological Age Applied at Ubberup

Evaluation and Validation of Biological Age as Health Technology

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04279366
Enrollment
83
Registered
2020-02-21
Start date
2020-11-15
Completion date
2022-06-06
Last updated
2024-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Aging, Lifestyle Risk Reduction

Keywords

Individualised Health, Prediction, Risk Assessment

Brief summary

In a previous study the investigators have developed a novel biological age model. Assessing biological age is the assessment of the present health status and functional capacity/physiological reserve of that person in comparison with people of the same age and sex. The aim of this study is to investigate the utility and validity of this novel biological age model designed for health promotion in real world conditions.

Detailed description

Study design: This is a longitudinal study, where biological age assessment is conducted in the first and final week of an 11-14 week lifestyle intervention course. These courses take place at a Danish folk high school (Ubberup), which is specialized in performing intensive lifestyle interventions targeting a 10% weight loss. The intention is to include 80 adult men and women. Data collection: This will take place at the facilities at Ubberup folk high school, participants being overnight fasted and without having exercised for the previous 24 hours. All analysis will be performed in investigators lab (Xlab) at the Department of Biomedical Sciences, Copenhagen University. When all samples are analysed Biological age will be calculated for each particpant.

Interventions

BEHAVIORALLifestyle intervention

The 14 week courses takes place at a Danish folk high school (Ubberup), specialized in lifestyle interventions targeting a 10% weight loss. Adult individuals with obesity sign up for the course. They stay at the School for the whole course period and the total cost amounts to 300-400 Euros per week plus loss of income.

Sponsors

Technical University of Denmark
CollaboratorOTHER
University of Copenhagen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Participation in a long course at Ubberup folk high school (12-15 weeks) * Age between 18-65 years

Exclusion criteria

* Previous or current cardiovascular disease * Pregnancy * Conditions that prevents from performing a cycle and/or strength tests

Design outcomes

Primary

MeasureTime frameDescription
Change in biological ageweek1 and week 14a composite score predicting risk of lifestyle related diseases

Secondary

MeasureTime frameDescription
Change in cardiorespiratory capacityweek 1 and week 14VO2max maximal oxygen consumption (ml/min/kg
Change in strengthweek 1 and week 14Hand grip, isometric quadriceps and biceps strength (Nm)
Change in Sit to Stand testweek 1 and week 14Rise and sit from a chair as many times as possible during 1 minute (number og rises)
Change in Central obesityweek 1 and week 14Waist to hip ratio is measured by dividing waist circumference with hip circumference in cm.
Change in body weightweek 1 and week 14measured in kilograms
Change in body compositionweek 1 and week 14BMI (kg/m2) is calculated
Change in fat massweek 1 and week 14fat mass(g) is assessed by bioimpedance
Change in fat percentageweek 1 and week 14Fat%, is assessed by bioimpedance
Change in Advanced glycation endproductsweek 1 and week 14Levels of glycated protein and lipids as a result of exposure of excess sugars advanced glycation endproducts (AGE) measured in the skin
Change in HormonesWeek 1 and week 14Insulin
Change in muscle massweek 1 and week 14muscle mass(g) is assessed by bioimpedance
Change in lipid profileweek 1 and week 14HighDensityLipoprotein (mmol/L), LowDensityLipoprofile (mmol/L), TriGlycerides (mmol/L), FreeFattyAcids (mmol/L) and Glycerol (mmol/L) is measured in a blood sample.
Change in Inflammatory profileweek 1 and week 14C-reactive protein mg/L, soluble urokinase plasminogen activating receptor ng/ml, InterLeukin 6 and 8 (pg/mL), tumor necrosis factor (pg/mL), Leptin and Adiponectin (ng/ml) is analysed from blood samples
Change in Blood glucoseweek 1 and week 14HbA1c and fasting glucose (mmol/L) measured from blood sample
Change in Respirometryweek 1 and week 14forced vital capacity and forced expiratory volume at one second(L)
Change in Blood Pressureweek 1 and week 14Systolic and Diastolic blood pressure (mmHg)

Other

MeasureTime frameDescription
Change in Metabolic Syndrome occurrenceweek 1 and week 14A cluster of 5 risk factors predicting risk of CVD and T2D
Change in Framingham Risk Scoreweek 1 and week 14A composite score predicting 10 years risk of future CVD

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026