Sedentary Behavior Clinical Trial
— ACTLIFEOfficial title:
ACTLIFE: is Active Life-style Enough for Health and Wellbeing in Elderly?
Sedentary lifestyles in modern obesogenic society produce several dysfunctions that cause chronic diseases in lederly population and this phenomenon is becoming a major public health problem. Regular physical activity has a profound effect on the expression of the potentials of human resilience, resulting in a decreased risk of chronic diseases. The identification of the biological mechanisms that are candidates for exercise-induced health benefits through biological pathways that are largely different from those targeted by common drugs, is highly relevant, since it might help to improve our knowledge of the pathophysiology of the chronic diseases in the sedentary population as well as to maximize the efficacy of physical activity interventions by implementing the best possible exercise dosage in older adults. For this purpose, the first aim of this project will be to identify the bioactive molecules and functional mechanisms that are candidates for exercise-induced health benefits. Moreover, in the view of more reliable, ecological and tailored approaches to counteract the problem of sedentary lifestyle, the second aim of this project will be to evaluate the effectiveness of an ecological exercise intervention in comparison to a traditional exercise intervention in sedentary elderly individuals.
Status | Not yet recruiting |
Enrollment | 180 |
Est. completion date | February 28, 2023 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 65 Years to 99 Years |
Eligibility | Inclusion Criteria: - for sedentary individuals: =700 METs/week measured by IPAQ - for active individuals: =1000 METs/week measured by IPAQ Exclusion Criteria: - Presence of cardiovascular and respiratory diseases - Presence of Hypertension - Presence of neurodegenerative diseases - Pesence of acuteor chronic conditions that might influence inlfammatory response - Any vascular Diabetes-related complication - Drugs or alchol abuse - Presence of other health-related condition that might affect the practice of physical activity. |
Country | Name | City | State |
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Italy | University of Verona | Verona |
Lead Sponsor | Collaborator |
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Universita di Verona |
Italy,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Measure of strandars healthy-related biochemical parameters | Blood samples will be collected two times: 1) between 7:00 and 9:00 am, following overnight fasting, 48h distant from the last exercise session and 2) immediately after a training session. After centrifugation, they will be divided in different aliquots of appropriate amount and stored a -80°C in order to: measure triglycerides, total cholesterol, blood glucose, aspartate transaminase, alanine transaminase, creatinine | through study completion, an average of 8 months | |
Secondary | Measure of Daily Energy Expenditure | Each participant will be outfitted with an Actiheart device allowing heart rate and acceleration data to be simultaneously recorded 24 hours a day for 7 consecutive days.
Health-related quality of life: The Italian version of the SF-36 health survey will be administrated before and after the interventions. |
through study completion, an average of 8 months | |
Secondary | Measure of the appendicular muscle mass | Magnetic resonance imaging (MRI) will be performed using a 1.5 Tesla MRI system. T1-weighted images of the lower limbs will be acquired supine with the legs extended. On the basis of a signal-intensity threshold, muscle borders will be selected to delineate and differentiate muscle, fat, and connective tissue. In the thighs area, the vastus lateralis (VL), vastus medialis, vastus intermedius, and rectus femoris will be traced in each image and in combination made up the quadriceps. Quadriceps muscle volumes will be calculated by summing the areas of all the slices. | through study completion, an average of 8 months | |
Secondary | Measure of Musle architecture | In the thigh, sagittal ultrasound images of the VL muscle will be recorded with a GE ultrasound system (GE Logiq-7) equipped with an 8-12 MHz linear transducer. Images will be obtained with a 90° flexion of hip and knee, at 50% of femur length corresponding to the mid-belly of the VL muscle. The pennation angle of the VL fascicles will be measured as the angle between the VL muscle fascicles and the deep aponeurosis of the insertion. | through study completion, an average of 8 months | |
Secondary | Measure of systemic vascular function | The passive limb movement protocol consisted of 60 s of resting baseline femoral blood flow data collection, followed by 60 s of passive knee extension and flexion with the same measure. Blood velocity will be analyzed with 1 Hz resolution on the Doppler ultrasound system (GE Logiq-7) for 60 s at rest and second by second for the first 60 s following the initiation of PLM. | through study completion, an average of 8 months | |
Secondary | Measure of cirulating level of hormones | Blood samples will be collected two times: 1) between 7:00 and 9:00 am, following overnight fasting, 48h distant from the last exercise session and 2) immediately after a training session. After centrifugation, they will be divided in different aliquots of appropriate amount and stored a -80°C in order to: measure cirulatin glevels of hormones such as: GH, IGF-1, IGFBP3, insulin and cortisol; the pro- and anti-inflammatory markers, C Reactive Protein (CRP), IL-1, IL-6 and IL-1ra; and of the sex-hormones testosterone, oestradiol, oestrone and sex hormone-binding globulin (SHBG); | through study completion, an average of 8 months | |
Secondary | Measure of cirulating bioactive markers | Blood samples will be collected two times: 1) between 7:00 and 9:00 am, following overnight fasting, 48h distant from the last exercise session and 2) immediately after a training session. After centrifugation, they will be divided in different aliquots of appropriate amount and stored a -80°C in order to measure circulating miRNA, PGC-1, Myonectin, Musclin, Sparc, Myostatin, BDNF, VEGF, and BDNF | through study completion, an average of 8 months | |
Secondary | Measure of cardio-metabolid health | Measurements of blood pressure will be performed with standard auscultatory and mercury sphygmomanometer technique.
From a fasted venous blood sample Glucose, high- and low-density lipoprotein will be measured on a Cobas c501 (Roche Diagnostics GmbH, Mannheim, Germany), using proprietary reagents. Body anthropometrics will be measured with a standard protocol: body mass, height, body mass index calculation (BMI = body mass / height2), percent of body fat (7 skinfolds approach), waist and hip circumferences. |
through study completion, an average of 8 months | |
Secondary | Measure of exercise capacity | To determine exercise capacity the subjects will perform an incremental walking maximal exercise trial (rest, 25%, 50%, 75%, and 100% of maximal exercise capacity). Breath-by-breath O2 expiratory airflow will be continuously recorded at rest, and during the exercise trial. | through study completion, an average of 8 months | |
Secondary | Measure of Lower limbs neuromuscular control | The force and EMG envelope rate of development during a maximum voluntary contraction and a tetanic stimulation will be compared in order to estimate the role of central command flow to the muscle in changing the efficiency of the tension development at the tendon. The maximal voluntary contraction will be started after a visual command will be done. | through study completion, an average of 8 months |
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