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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04279366
Other study ID # UbberupBioAge
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 15, 2020
Est. completion date June 6, 2022

Study information

Verified date February 2024
Source University of Copenhagen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 83
Est. completion date June 6, 2022
Est. primary completion date June 6, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Lifestyle 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.

Locations

Country Name City State
Denmark Xlab, Faculty of Health and Medical Sciences, University of Copenhagen Copenhagen
Denmark Ubberup High School Kalundborg Danmark

Sponsors (2)

Lead Sponsor Collaborator
University of Copenhagen Technical University of Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in Metabolic Syndrome occurrence A cluster of 5 risk factors predicting risk of CVD and T2D week 1 and week 14
Other Change in Framingham Risk Score A composite score predicting 10 years risk of future CVD week 1 and week 14
Primary Change in biological age a composite score predicting risk of lifestyle related diseases week1 and week 14
Secondary Change in cardiorespiratory capacity VO2max maximal oxygen consumption (ml/min/kg week 1 and week 14
Secondary Change in strength Hand grip, isometric quadriceps and biceps strength (Nm) week 1 and week 14
Secondary Change in Sit to Stand test Rise and sit from a chair as many times as possible during 1 minute (number og rises) week 1 and week 14
Secondary Change in Central obesity Waist to hip ratio is measured by dividing waist circumference with hip circumference in cm. week 1 and week 14
Secondary Change in body weight measured in kilograms week 1 and week 14
Secondary Change in body composition BMI (kg/m2) is calculated week 1 and week 14
Secondary Change in fat mass fat mass(g) is assessed by bioimpedance week 1 and week 14
Secondary Change in fat percentage Fat%, is assessed by bioimpedance week 1 and week 14
Secondary Change in muscle mass muscle mass(g) is assessed by bioimpedance week 1 and week 14
Secondary Change in lipid profile HighDensityLipoprotein (mmol/L), LowDensityLipoprofile (mmol/L), TriGlycerides (mmol/L), FreeFattyAcids (mmol/L) and Glycerol (mmol/L) is measured in a blood sample. week 1 and week 14
Secondary Change in Inflammatory profile C-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 week 1 and week 14
Secondary Change in Blood glucose HbA1c and fasting glucose (mmol/L) measured from blood sample week 1 and week 14
Secondary Change in Respirometry forced vital capacity and forced expiratory volume at one second(L) week 1 and week 14
Secondary Change in Blood Pressure Systolic and Diastolic blood pressure (mmHg) week 1 and week 14
Secondary Change in Advanced glycation endproducts Levels of glycated protein and lipids as a result of exposure of excess sugars advanced glycation endproducts (AGE) measured in the skin week 1 and week 14
Secondary Change in Hormones Insulin Week 1 and week 14
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