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Effectiveness Multicomponent Exercise Programme in Older Subjects. A Pilot Study.

Primary Purpose

Old Age; Debility, Sarcopenia, Exercise Addiction

Status
Not yet recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Multicomponent Training
Sponsored by
Universitat Internacional de Catalunya
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Old Age; Debility

Eligibility Criteria

65 Years - 95 Years (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Sedentary persons between 65 and 95 years of age.
  • Have a walking speed ≤0.8 metres per second as this is characteristic of patients with or with onset of sarcopenia.
  • Have a grip strength <30 kg for men and <20 kg for women as being characteristic of patients with or with onset of sarcopenia.

Exclusion Criteria:

  • Severe untreated osteoporosis.
  • Having suffered a bone fracture in the last year.
  • Having had juvenile osteoporosis during adolescence or young adulthood.
  • Active chronic pathology
  • Uncontrolled arterial hypertension.
  • Uncontrolled orthostatic hypotension.
  • Severe acute respiratory failure.
  • Diabetes mellitus with acute decompensation or uncontrolled hypoglycaemia.
  • Endocrine, haematological and other associated rheumatic diseases.
  • Mental health problems (schizophrenia, dementia, depression, etc.) or not being in full mental capacity.
  • Patients with pharmacological treatments of glucocorticoids, anticoagulants and/or diuretics.
  • Patients with coagulation problems or previous cardiac pathology.
  • People with a body mass index (BMI) of 30 or more.
  • Subjects with a systemic disease or any other pathology in which therapeutic exercise may be contraindicated.

Sites / Locations

  • Universitat Internacional de Catalunya

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Multicomponent Training

Arm Description

Traditional training. 3 times a week Warm-up: Main work: Aerobic training Strength training Balance and coordination training Return to calm

Outcomes

Primary Outcome Measures

Functionality (Running speed in 4 metres. Seconds)
The participant's speed in covering 4 metres at their usual walking speed is assessed. The shorter the time, the faster the walking speed and therefore the better the functionality.
Functionality (Timed get up and go. Seconds)
The time it takes the participant to get up from a chair, walk 3 metres, turn around an obstacle (a cone) and sit back down in the chair is assessed. The less time the participant takes to perform the test, the better the functionality.

Secondary Outcome Measures

Functionality (Short Physical Performance Battery. 0-12 points)
It consists of a battery of three exercises with a maximum score of 4 points each. The first exercise assesses the participant's balance, the second exercise assesses walking speed and the third exercise assesses the strength of the lower limbs to stand up and sit down from the chair. The maximum SPPB score is 12 points indicating excellent functionality.
Neuromuscular Function, Handgrip (Kg)
A hand-held dynamometer shall be used to assess the maximum grip force for 5 seconds. The participant shall squeeze the dynamometer as hard as possible and the dynamometer shall record the force applied.
Neuromuscular Function, Myotonometry (Stiffness)
Myotonometry is an instrument that assesses the viscoelasticity of tissue by means of a mechanical impulse in the muscle belly. The device generates a small mechanical impulse in the muscle belly and, depending on the response of the muscle belly to this stimulus, provides the variable stiffness.
Neuromuscular Function,Tensiomyography (Radial displacement (Dm)).
Tensiomyography is an instrument which, at a given power, generates an involuntary muscle contraction in the muscle under examination. The contraction causes a movement of the muscle belly in a radial direction which is detected by a mechanical sensor placed just in contact with the muscle. The mechanical sensor collects the variables of radial displacement (Dm).
Neuromuscular Function,Tensiomyography (Shrinkage time (Tc))
Tensiomyography is an instrument which, at a given power, generates an involuntary muscle contraction in the muscle under examination. The contraction causes a movement of the muscle belly in a radial direction which is detected by a mechanical sensor placed just in contact with the muscle. The mechanical sensor collects the variables of contraction time (Tc).

Full Information

First Posted
February 25, 2022
Last Updated
March 17, 2022
Sponsor
Universitat Internacional de Catalunya
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1. Study Identification

Unique Protocol Identification Number
NCT05286723
Brief Title
Effectiveness Multicomponent Exercise Programme in Older Subjects. A Pilot Study.
Official Title
Effectiveness Multicomponent Exercise Programme in Older Subjects. A Pilot Study.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 1, 2022 (Anticipated)
Primary Completion Date
May 15, 2022 (Anticipated)
Study Completion Date
June 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitat Internacional de Catalunya

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Sarcopenia can occur or increase due to sedentary lifestyles, physical inactivity or chronic endocrine and inflammatory disorders, this pathology is much more frequent in older people due to the added risk factors and the fact that the physiological ageing process generates a pro-inflammatory situation and an alteration in the synthesis of hormones and myokines, it has been observed that the loss of strength causes functional deterioration and a significant increase in the person's dependence, reduces their functional status and quality of life, and may increase the risk of falls, thereby increasing mortality. The hipotesis of this study is that multicomponent training 3 times a week for 6 weeks, produces improvements in the functional capacity of elderly patients. This study has the objective is whether multicomponent training 3 times a week for 6 weeks produces improvements in the functional capacity of elderly patients. The methodology is a pilot clinical trial. The study population is people over 65 years of age, sedentary, with functional independence and with a state of health that allows them to carry out physical activity. The study is planned as a pilot study and will consist of 13 subjects in the experimental group (multicomponent training). The variables to be measured are anthropometric variables and variables of neuromuscular function an functionality. The intervention will be a training will be 3 times a week during 6 weeks, with a warm-up, a main block with aerobic work, strength work and training and coordination work, and finally a return to calm.
Detailed Description
Sarcopenia can occur or increase due to sedentary lifestyles, physical inactivity or chronic endocrine and inflammatory disorders, this pathology is much more frequent in older people due to the added risk factors and the fact that the physiological ageing process generates a pro-inflammatory situation and an alteration in the synthesis of hormones and myokines, it has been observed that the loss of strength causes functional deterioration and a significant increase in the person's dependence, reduces their functional status and quality of life, and may increase the risk of falls, thereby increasing mortality. The hipotesis of this study is that multicomponent training 3 times a week for 6 weeks, produces improvements in the functional capacity of elderly patients. This study has the objective is whether multicomponent training 3 times a week for 6 weeks produces improvements in the functional capacity of elderly patients. The methodology is a pilot clinical trial. The study population is people over 65 years of age, sedentary, with functional independence and with a state of health that allows them to carry out physical activity. The study is planned as a pilot study and will consist of 13 subjects in the experimental group (multicomponent training). The variables to be measured are anthropometric variables and variables of neuromuscular function an functionality. The variables to be measured are anthropometric variables such as height, sex, age, lower limb dominance and bioimpedance, we will also measure variables of neuromuscular function, with Tensiomyography: Contraction time (Tc), and radial displacement (Dm), Myotonometry: Stiffness, Surface electromyography: %RMS, all of this in muscles Rectus femoris, vastus lateralis, vastus medialis, lateral gastrocnemius and tibialis anterior. Manual dynamometry: Peak force (Kg) grip strength (Handgrip). Information on functionality with Short Physical Performance Battery (SPPB), velocity in 4 meters walking, Timed get up and go (TUG). The intervention will be a training will be 3 times a week during 6 weeks, with a warm-up, a main block with aerobic work, strength work and training and coordination work, and finally a return to calm. The intervention will be a training 3 times a week with, warm up, articular and functional exercises with one's own body weight, principal work: Aerobic training 20 minutes waking then strenght training 25 minutes, i.Sets: start with 1 set to consolidate the technique, and progress to 3 sets. ii.Repetitions: start with 10-15 repetitions (at lower intensity) and progress to 8-12 repetitions. iii.Intensity: start with a lower intensity (even 20-30%1RM) and progress to 70-80%1RM. iv.Rest: Breaks between sets of 3-5 minutes should be taken to avoid muscle fatigue. v.Exercises: Leg press on machine Balance and co-ordination training during 5-10 minutes finally return to calm during 5 minutes with stretching.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Old Age; Debility, Sarcopenia, Exercise Addiction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Multicomponent Training
Arm Type
Experimental
Arm Description
Traditional training. 3 times a week Warm-up: Main work: Aerobic training Strength training Balance and coordination training Return to calm
Intervention Type
Other
Intervention Name(s)
Multicomponent Training
Intervention Description
Warm up, aerobic training, stenght training, balance and coordination training and return to calm
Primary Outcome Measure Information:
Title
Functionality (Running speed in 4 metres. Seconds)
Description
The participant's speed in covering 4 metres at their usual walking speed is assessed. The shorter the time, the faster the walking speed and therefore the better the functionality.
Time Frame
Change between baseline and 6 weeks
Title
Functionality (Timed get up and go. Seconds)
Description
The time it takes the participant to get up from a chair, walk 3 metres, turn around an obstacle (a cone) and sit back down in the chair is assessed. The less time the participant takes to perform the test, the better the functionality.
Time Frame
Change between baseline and 6 weeks
Secondary Outcome Measure Information:
Title
Functionality (Short Physical Performance Battery. 0-12 points)
Description
It consists of a battery of three exercises with a maximum score of 4 points each. The first exercise assesses the participant's balance, the second exercise assesses walking speed and the third exercise assesses the strength of the lower limbs to stand up and sit down from the chair. The maximum SPPB score is 12 points indicating excellent functionality.
Time Frame
Change between baseline and 6 weeks
Title
Neuromuscular Function, Handgrip (Kg)
Description
A hand-held dynamometer shall be used to assess the maximum grip force for 5 seconds. The participant shall squeeze the dynamometer as hard as possible and the dynamometer shall record the force applied.
Time Frame
Change between baseline and 6 weeks
Title
Neuromuscular Function, Myotonometry (Stiffness)
Description
Myotonometry is an instrument that assesses the viscoelasticity of tissue by means of a mechanical impulse in the muscle belly. The device generates a small mechanical impulse in the muscle belly and, depending on the response of the muscle belly to this stimulus, provides the variable stiffness.
Time Frame
Change between baseline and 6 weeks
Title
Neuromuscular Function,Tensiomyography (Radial displacement (Dm)).
Description
Tensiomyography is an instrument which, at a given power, generates an involuntary muscle contraction in the muscle under examination. The contraction causes a movement of the muscle belly in a radial direction which is detected by a mechanical sensor placed just in contact with the muscle. The mechanical sensor collects the variables of radial displacement (Dm).
Time Frame
Change between baseline and 6 weeks
Title
Neuromuscular Function,Tensiomyography (Shrinkage time (Tc))
Description
Tensiomyography is an instrument which, at a given power, generates an involuntary muscle contraction in the muscle under examination. The contraction causes a movement of the muscle belly in a radial direction which is detected by a mechanical sensor placed just in contact with the muscle. The mechanical sensor collects the variables of contraction time (Tc).
Time Frame
Change between baseline and 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sedentary persons between 65 and 95 years of age. Have a walking speed ≤0.8 metres per second as this is characteristic of patients with or with onset of sarcopenia. Have a grip strength <30 kg for men and <20 kg for women as being characteristic of patients with or with onset of sarcopenia. Exclusion Criteria: Severe untreated osteoporosis. Having suffered a bone fracture in the last year. Having had juvenile osteoporosis during adolescence or young adulthood. Active chronic pathology Uncontrolled arterial hypertension. Uncontrolled orthostatic hypotension. Severe acute respiratory failure. Diabetes mellitus with acute decompensation or uncontrolled hypoglycaemia. Endocrine, haematological and other associated rheumatic diseases. Mental health problems (schizophrenia, dementia, depression, etc.) or not being in full mental capacity. Patients with pharmacological treatments of glucocorticoids, anticoagulants and/or diuretics. Patients with coagulation problems or previous cardiac pathology. People with a body mass index (BMI) of 30 or more. Subjects with a systemic disease or any other pathology in which therapeutic exercise may be contraindicated.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jacobo Rodríguez-Sanz, PhD
Phone
+34636136789
Email
jrodriguezs@uic.es
Facility Information:
Facility Name
Universitat Internacional de Catalunya
City
Sant Cugat Del Vallès
State/Province
Barcelona
ZIP/Postal Code
08195
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Albert Pérez-Bellmunt, PhD
Phone
636817297
Email
aperez@uic.es

12. IPD Sharing Statement

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Effectiveness Multicomponent Exercise Programme in Older Subjects. A Pilot Study.

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