Aging Well Clinical Trial
Official title:
Strength Training in Hypoxia to Improve Bone and Cardiovascular Health of Elderly
NCT number | NCT04281264 |
Other study ID # | IB18010 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 9, 2019 |
Est. completion date | June 30, 2021 |
Verified date | July 2021 |
Source | University of Extremadura |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Due to age-related effects, the bone and cardiovascular health are damaged. Physical exercise and in particular the strength training has been proposed as a fundamental tool to these pathologies, especially in the elderly. On the other hand, the use of normobaric hypoxia combined with exercise could have a beneficial synergistic effect on disease prevention and the quality of life of the elderly. Therefore, the general objective of this project is to analyze the effects of different methods of strength training combined with conditions of normobaric hypoxia on the bone and cardiovascular health of the elderly. This general objective is specified in the following specific objectives: - To analyze the effects of circuit training with elastic bands on bone mineral density and bone remodelling markers of elderly, under normoxic and normobaric hypoxic conditions. - To analyze the effects of circuit training with elastic bands on biochemical parameters, inflammatory, endothelial and clinical markers just like cardiovascular risk level of elderly, under normoxic and normobaric hypoxic conditions. - To analyze the effects of circuit training with elastic bands on body composition and functional capacity of elderly, under normoxic and normobaric hypoxic conditions. - To analyze the effects of whole-body vibration training on bone mineral density and bone remodelling markers of elderly, under normoxic and normobaric hypoxic conditions. - To analyze the effects of whole-body vibration training on biochemical parameters, inflammatory, endothelial and clinical markers just like cardiovascular risk level of elderly, under normoxic and normobaric hypoxic conditions. - To analyze the effects of whole-body vibration training on body composition and functional capacity of elderly, under normoxic and normobaric hypoxic conditions. - To compare the effects of circuit training with elastic bands versus whole-body vibration training on bone and cardiovascular health of elderly, under normoxic and normobaric hypoxic conditions. - To value the normobaric hypoxic environment efficacy on bone and cardiovascular health of elderly subjected to circuit training with elastic bands and whole-body vibration training. We hypothesize that bone and cardiovascular health will improve in the participants subjected to both resistance training, but greater improved may be found when these protocol are combined with normobaric hypoxia.
Status | Completed |
Enrollment | 120 |
Est. completion date | June 30, 2021 |
Est. primary completion date | June 30, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 65 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. women and men aged 65 years or older 2. no current medical condition not compatible with planned exercise 3. free of illness or medication potentially affecting the bone and cardiovascular system 4. estimated daily calcium intake of 1200-2000 mg/day 5. consumption of no more than two alcoholic beverages per day. Exclusion Criteria: 1. participation in any other type of intervention based on physical exercise in the last 6 months in order to avoid interactions with the previous practice 2. subjects have been above 1500 m during the last 3 months 3. contra indications for whole-body vibration training: severe cardiovascular diseases, ocular diseases that affect the retina, neuromuscular and heart diseases, stroke, implant, bypass, stent, arthritis and other joint disease or epilepsy |
Country | Name | City | State |
---|---|---|---|
Spain | Sport Science Faculty. University of Extremadura | Cáceres |
Lead Sponsor | Collaborator |
---|---|
University of Extremadura |
Spain,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline Life Quality at 24 weeks | SF-36 questionnaire will be used to know the life quality | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Risk of Fall at 24 weeks | Risk of fall will be evaluated through Fall Efficacy Scale-International (FES-I) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Blood Pressure at 24 weeks | Blood pressure (mmHg) will be measured with sphygmomanometer | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Cardiovascular Evaluation at 24 weeks | Arm-ankle index and pulse wave velocity will be measured using ultrasound Doppler technique | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Cardiovascular Risk at 24 weeks | Based on the following factors: age, sex, smoking, total cholesterol, HDL cholesterol, systolic blood pressure and diabetes, cardiovascular risk will be determined. This method was already described in the FRESCO study | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Weight at 24 weeks | Weight (kilograms) will measure following standard procedures | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Height at 24 weeks | Height (meters) will measure following standard procedures | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Body Mass Index at 24 weeks | Weight and Height will be combined to report body mass index (BMI) in kg/m^2 | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Waist-Hip Ratio at 24 weeks | Waist and hip diameter (centimeters) will be combined to report Waist-Hip Ratio | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Body Composition at 24 weeks | Body composition variables such as percentage fat and lean fat mass (percentage) will be obtain using dual-energy X-ray absorptiometry (DXA,Norland Excell Plus; Norland Inc., Fort Atkinson, United States). | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Bone Mineral Density at 24 weeks | Bone mineral density (g/cm-2) of whole body and proximal femur region will be calculated from obtained data of dual-energy X-ray absorptiometry (DXA,Norland Excell Plus; Norland Inc., Fort Atkinson, United States) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Osteoporosis/Osteopenia Prevalence at 24 weeks | T-score of whole body and proximal femur region will be calculated from obtained data of dual-energy X-ray absorptiometry (DXA,Norland Excell Plus; Norland Inc., Fort Atkinson, United States) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Bone Mineral Content at 24 weeks | Bone mineral content (g) of whole body and proximal femur region will be calculated from obtained data of dual-energy X-ray absorptiometry (DXA,Norland Excell Plus; Norland Inc., Fort Atkinson, United States) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Biochemical Parameters at 24 weeks | Standard biochemical analysis (HDL, LDL and Total Cholesterol, Triglycerides and Glucose in mg/dL) will be obtained of blood samples, through a clinical chemistry analyzer (Spotchem, Arkray Factory, Germany) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Bone Remodelling Markers at 24 weeks | Bone remodelling (VEGF and SDF-1 in mg/dL) markers will be analyzed by ELISA technique. | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Inflammatory Markers at 24 weeks | Inflammatory (C-reactive protein, IL-2, IL-4, IL-6 and TNFa in mg/dL) markers will be analyzed by ELISA technique. | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Endothelial Markers at 24 weeks | Endothelial (ICAM-1 and VCAM-1 in mg/dL) markers will be analyzed by ELISA technique. | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Lower Limb Strength at 24 weeks | Senior Fitness Test battery will be used to know of physical condition of elderly. Lower limb strength will be tested by Chair stand Test (repetitions) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Upper Limb Strength at 24 weeks | Senior Fitness Test battery will be used to know of physical condition of elderly. Upper limb strength will be tested by Arm curl Test (repetitions) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Lower Limb Flexibility at 24 weeks | Senior Fitness Test battery will be used to know of physical condition of elderly. Lower limb flexibility will be tested by Chair sit and reach Test (centimeters) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Upper Limb Flexibility at 24 weeks | Senior Fitness Test battery will be used to know of physical condition of elderly. Upper limb flexibility will be tested by Back scratch Test (centimeters) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Endurance at 24 weeks | Senior Fitness Test battery will be used to know of physical condition of elderly. Endurance will be tested by 6 min. walk Test (meters) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Agility at 24 weeks | Senior Fitness Test battery will be used to know of physical condition of elderly. Agility will be tested by 8ft Up and Go Test (seconds). | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Core muscle strength at 24 weeks | Core muscle strength will be tested by plank test (seconds) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Grip strength at 24 weeks | Grip strength will be tested using an Handgrip (kilograms) | Through study completion, an average of 24 weeks | |
Primary | Change from Baseline Balance at 24 weeks | Balance will be tested by single leg stance test (seconds) | Through study completion, an average of 24 weeks | |
Secondary | Socio-Demographic Data | A general questionnaire was administered to collect medical and demographic data to check the inclusion/exclusion criteria. | Baseline | |
Secondary | Change from Baseline Calcium Intake at 24 weeks | Calcium intake (mg/day) will be estimated using a food frequency questionnaire | Through study completion, an average of 24 weeks | |
Secondary | Change from Baseline Physical Activity Level at 24 weeks | The bone-specific physical activity questionnaire (B-PAQ; score) will be used to assess the physical activity level of the participants. | Through study completion, an average of 24 weeks |
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