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Viability of an Educational Program for Lifestyle Changes and an Algorithm for the Derivation of Exercise Programs in Older People at Risk of Dependency at Primary Care. (PRICA-POWFRAIL)

Primary Purpose

Frailty, Disability Physical, Old Age; Atrophy

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
EDUcation
EXERcise
EDU-EXER
CONtrol
Sponsored by
University of Cadiz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Frailty focused on measuring Education, Physical Exercise, Aging, Frailty, Dependency, Biomarkers, Older Adults, Machine Learning

Eligibility Criteria

70 Years - 99 Years (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Following the 2014 Consensus Document on the prevention of frailty and falls in the elderly patient we will recruit individuals I) > 70 years of age II) with a Barthel Index score > 75 III) meeting at least one of the following two criteria: a score ≤9 in the short physical performance battery (SPPB) or FRAIL questionnaire with values 1 or 2. Exclusion Criteria: I) Inability to go to the Primary Care Health Centre for any reason. II) Moderate to severe cognitive impairment (Mini-Mental State Examination< 20 points III) Severe pathology for which physical activity is contraindicated at the physician's discretion including but not limited to: recent acute myocardial infarction (6 months), uncontrolled cardiac arrhythmia, severe cardiac valve disease, non-controlled hypertension (> 180/100mmHg), non-controlled/severe heart failure, severe respiratory insufficiency disease, and diabetes mellitus with acute decompensation/frequent hypoglycaemia.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Experimental

    Active Comparator

    Arm Label

    EDUcation

    EXERcise

    EDU-EXER

    CONtrol

    Arm Description

    The EDU group will assist to an individualized educative program based on intrinsic capacity optimization through lifestyle changes.

    The EXER group will follow a program focused on the specific deficit of muscular power from a simple clinical test such as the STS and, in addition, they will be evaluated to be able to prescribe training individually (evaluation of training)

    EDU-EXER group subject develops both interventions together.

    CON group will continue the usual clinical treatment and their normal life.

    Outcomes

    Primary Outcome Measures

    Relative lower limbs muscle power
    The STS muscle power test was used to assess mechanical power. Participants were instructed to perform 5 timed STS repetitions after the cue "ready, set, go!", as fast as possible, on a standardized armless chair (height = 0.43 m) with arms crossed over the chest. Importantly, from the sitting position, they had to fully extend their knees and hips to the standing position, and descend to the sitting position until at least touching the chair with their buttocks. The test was repeated when any of these instructions was broken. The time (±0.01 s) needed to perform 5 STS repetitions was recorded using a stopwatch. Absolute STS muscle power (W) was calculated using an equation where body mass is indicated in kg, body height and chair height in m, and five STS time in s (Alcazar et al. 2018). Alcazar, J. et al. The sit-to-stand muscle power test: An easy, inexpensive and portable procedure to assess muscle power in older people. Exp Gerontol 112, 38-43 (2018).
    Vital functional capacity
    The vital functional capacity will be evaluated through cardiorespiratory function using an indirect test adapted to the age range (field tests, which allow obtaining an estimated value of maximum oxygen consumption, the best integral marker of the physiological reserve of an individual, namely 6minute walking test or the 2 min-version which is highly correlated.
    Level of physical activity during the daily life
    Measured by accelerometry for 1 week in evaluation timepoints.

    Secondary Outcome Measures

    The quality of life (QoL)
    EQ-5D which measures health-related QoL through physical, psychological and social dimensions.
    Subjective health-status level
    SF-36 questionnaire which measures the subjective health-status level.
    Cognitive Function - Mini-mental state examination (MMSE)
    The mini-mental test is a simple test that allows detecting the presence of cognitive impairment, that is, of dementia. It can be normal in people with mild cognitive impairment or with incipient forms of Alzheimer's requiring, in these cases, studies with more sophisticated tests.
    Cognitive Function - The Montreal cognitive assessment test (MoCA)
    The Montreal cognitive assessment test (MoCA) is a brief instrument with which, in a specific way, mild cognitive impairment is detected, as well as dementia.
    Mood State - Geriatric Depression Scale (GDS)
    The Geriatric Depression Scale (GDS) is a self-report measure of depression in older adults. Users respond in a "Yes/No" format. The GDS was originally developed as a 30-item instrument. Since this version proved both time-consuming and difficult for some patients to complete, a 15-item version was developed.
    Nutritional profile measurements - Mediterranean Diet Adherence Screener index
    1. MEDAS (Mediterranean Diet Adherence Screener index). Scale of adherence to the Mediterranean diet of 14 items.
    Degree of frailty - Fried criteria
    The Fried frailty phenotype (FP) assesses physical frailty through five criteria: unintentional weight loss; weakness or poor handgrip strength; self-reported exhaustion; slow walking speed; and low physical activity.
    Body composition - Bioimpedance
    The body composition will be evaluated by means of bioimpedance.
    Body composition - body mass index (BMI)
    Weight and height will be combined to report BMI in kg/m^2
    Body composition - height
    Height measure in meter
    Body composition - weight
    Weight measure in kilograms
    Musculoskeletal ultrasound architecture
    All ultrasound images will be acquired by the same operator with the same ultrasound device throughout the whole study using a linear 40 mm transducer and a phased array transductor, and images will be analysed through the ACSAuto script to semi-automatically evaluate ultrasound pictures. The vastus lateralis architecture will be analysed through the Simple Muscle Architecture Analysis tool for Fiji. These procedures will be done according to Rodriguez-López et al. Rodriguez-Lopez, C. et al. Effects of Power-Oriented Resistance Training With Heavy vs. Light Loads on Muscle-Tendon Function in Older Adults: A Study Protocol for a Randomized Controlled Trial. Front Physiol 12, (2021).
    Depressive Symptoms
    The depressive symptoms will be assessed with the Geriatric Depression scale to assess psychology status of the participants.

    Full Information

    First Posted
    February 22, 2023
    Last Updated
    March 6, 2023
    Sponsor
    University of Cadiz
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05772910
    Brief Title
    Viability of an Educational Program for Lifestyle Changes and an Algorithm for the Derivation of Exercise Programs in Older People at Risk of Dependency at Primary Care.
    Acronym
    PRICA-POWFRAIL
    Official Title
    Viability of an Educational Program for Lifestyle Changes and an Algorithm for the Derivation of Exercise Programs in Older People at Risk of Dependency at Primary Care.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2023 (Anticipated)
    Primary Completion Date
    December 1, 2025 (Anticipated)
    Study Completion Date
    February 1, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Cadiz

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    According to the INE in 2021, more than 9 million people are currently over 65 years of age. This means that more than 1 million are frail and almost 4 million are pre-fragile only in Spain. Frailty is the prelude to disability and dependency, but unlike these, it is treatable and preventable. Currently, it is known that the best treatment for frailty is physical exercise and physical activity. The problem arises from the need that exists in the health system to prescribe individualized and patient-centered exercise, with the use of scarce resources (time, personnel, tools) and in a simple way in clinical practice. Additionally, the system needs tools that help us know (and predict) if this exercise prescription is efficient. Furthermore, frailty is a multidimensional syndrome, for which a comprehensive approach is necessary. The combined study of blood and digital biomarkers, as well as the plethora of dimensions evaluated (muscle and physical activity, cognitive, lifestyle, clinical, body composition, social, sleep), constitute an optimal approach that would provide a unique opportunity to understand prevention and treatment of unsuccessful aging and frailty. The PRICA-POWFRAIL project aims to examine the feasibility of an educational intervention to change lifestyle habits as well as the effect of a referral algorithm to an exercise program and lifestyle changes focused on treating specific deficits of low muscle power, powerful predictor of adverse health events. The subsequent referral will be implemented in a supervised exercise program at the functional, cognitive muscle level and in older people at risk of dependence. Secondarily, the effect of this intervention on blood biomarkers (at a genetic, epigenetic and metabolomic level), physical health (functional capacity, blood pressure, body composition) and mental health (quality of life and depression), as well as on other risk factors (genetic and biological) for the development of frailty. A total of 110 people older than 70 years of age in previous stages of dependency will be randomly distributed among the group of an educational program, the intervention group with supervised physical exercise, a intervention group with both previous educational and exercise programs and the control group. The design will include a 10- week intervention with pre and post-intervention measurement phases and a third measurement (retest) 12 months after completion. The supervised physical exercise program will be of a multi-component type including cardiovascular, muscular, coordinative and balance work, and a progression will be established in the different load parameters (frequency, volume, intensity, density). This will allow us to understand from a very complete perspective the causes and mechanisms underlying this response. The PRICA-POWFRAIL project Will mean a significant increase in scientific knowledge about the response and response rate to ultra-individualized exercise programs directed as a therapeutic measure in people at risk of dependency from a multidimensional perspective. In addition, the project will have a relevant impact at the social and economic level by transferring the findings of the study to the social and health field through the agents and means provided in it.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Frailty, Disability Physical, Old Age; Atrophy
    Keywords
    Education, Physical Exercise, Aging, Frailty, Dependency, Biomarkers, Older Adults, Machine Learning

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomized Control Trial
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    110 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    EDUcation
    Arm Type
    Experimental
    Arm Description
    The EDU group will assist to an individualized educative program based on intrinsic capacity optimization through lifestyle changes.
    Arm Title
    EXERcise
    Arm Type
    Experimental
    Arm Description
    The EXER group will follow a program focused on the specific deficit of muscular power from a simple clinical test such as the STS and, in addition, they will be evaluated to be able to prescribe training individually (evaluation of training)
    Arm Title
    EDU-EXER
    Arm Type
    Experimental
    Arm Description
    EDU-EXER group subject develops both interventions together.
    Arm Title
    CONtrol
    Arm Type
    Active Comparator
    Arm Description
    CON group will continue the usual clinical treatment and their normal life.
    Intervention Type
    Behavioral
    Intervention Name(s)
    EDUcation
    Other Intervention Name(s)
    EDU
    Intervention Description
    The education intervention will consist of an individualized educative program based on intrinsic capacity optimization through lifestyle changes. To develop the program, the program creation team will be multidisciplinary (psychologists, medical doctor, dietitian…) and will discuss goal setting, the education strategy, and retention of motivation. The experts are required to create the education program such that the participants can manage their health by themselves. The goal will be self-management of dietary habits and increases in physical activity levels for each individual case. The education program will be in Spanish or in English; as it will consist in personal counselling, even with a low level of the language the communication will be possible. The nutritional education program will be conducted every 2 weeks for 10 consecutive weeks, with 20-min counselling sessions by an expert.
    Intervention Type
    Other
    Intervention Name(s)
    EXERcise
    Other Intervention Name(s)
    EXER
    Intervention Description
    The intervention period will have 10 weeks, in which the EXER group will carry out 2-3 sessions a week (total of 20-30 sessions). In this concurrent program, exercises of the lower extremities (leg press, abduction and plantar flexion) will be performed mainly on weight training machines. Intensity in each exercise will be individualized for each participant through a test to determine muscle power. In addition, in the last part of each session the participants will perform an endurance training type high insensitive interval training on a cycle ergometer (60-80 rpm). The intensity will be individualized to each patient through an incremental stress test until volitional exhaustion, and the subjects will alternate intervals of 30 seconds at 90% of the maximum workload, with intervals of 90 seconds at 40% of the maximum. Each session is estimated to have a total duration of 30-50 minutes.
    Intervention Type
    Other
    Intervention Name(s)
    EDU-EXER
    Intervention Description
    This group will carry out the same two previous interventions together.
    Intervention Type
    Other
    Intervention Name(s)
    CONtrol
    Intervention Description
    CONtrol group will continue the usual clinical treatment and their normal life
    Primary Outcome Measure Information:
    Title
    Relative lower limbs muscle power
    Description
    The STS muscle power test was used to assess mechanical power. Participants were instructed to perform 5 timed STS repetitions after the cue "ready, set, go!", as fast as possible, on a standardized armless chair (height = 0.43 m) with arms crossed over the chest. Importantly, from the sitting position, they had to fully extend their knees and hips to the standing position, and descend to the sitting position until at least touching the chair with their buttocks. The test was repeated when any of these instructions was broken. The time (±0.01 s) needed to perform 5 STS repetitions was recorded using a stopwatch. Absolute STS muscle power (W) was calculated using an equation where body mass is indicated in kg, body height and chair height in m, and five STS time in s (Alcazar et al. 2018). Alcazar, J. et al. The sit-to-stand muscle power test: An easy, inexpensive and portable procedure to assess muscle power in older people. Exp Gerontol 112, 38-43 (2018).
    Time Frame
    Change from Baseline STS muscle power at 12 weeks
    Title
    Vital functional capacity
    Description
    The vital functional capacity will be evaluated through cardiorespiratory function using an indirect test adapted to the age range (field tests, which allow obtaining an estimated value of maximum oxygen consumption, the best integral marker of the physiological reserve of an individual, namely 6minute walking test or the 2 min-version which is highly correlated.
    Time Frame
    Change from Baseline Vital functional capacity at 12 weeks
    Title
    Level of physical activity during the daily life
    Description
    Measured by accelerometry for 1 week in evaluation timepoints.
    Time Frame
    Change from Baseline Level of physical activity at 12 weeks
    Secondary Outcome Measure Information:
    Title
    The quality of life (QoL)
    Description
    EQ-5D which measures health-related QoL through physical, psychological and social dimensions.
    Time Frame
    Change from Baseline the quality of life at 12 weeks
    Title
    Subjective health-status level
    Description
    SF-36 questionnaire which measures the subjective health-status level.
    Time Frame
    Change from Baseline the health status level at 12 weeks
    Title
    Cognitive Function - Mini-mental state examination (MMSE)
    Description
    The mini-mental test is a simple test that allows detecting the presence of cognitive impairment, that is, of dementia. It can be normal in people with mild cognitive impairment or with incipient forms of Alzheimer's requiring, in these cases, studies with more sophisticated tests.
    Time Frame
    Change from Baseline MMSE at 12 weeks
    Title
    Cognitive Function - The Montreal cognitive assessment test (MoCA)
    Description
    The Montreal cognitive assessment test (MoCA) is a brief instrument with which, in a specific way, mild cognitive impairment is detected, as well as dementia.
    Time Frame
    Change from Baseline MoCA at 12 weeks
    Title
    Mood State - Geriatric Depression Scale (GDS)
    Description
    The Geriatric Depression Scale (GDS) is a self-report measure of depression in older adults. Users respond in a "Yes/No" format. The GDS was originally developed as a 30-item instrument. Since this version proved both time-consuming and difficult for some patients to complete, a 15-item version was developed.
    Time Frame
    Change from Baseline Geriatric Depression Scale (GDS) at 12 weeks
    Title
    Nutritional profile measurements - Mediterranean Diet Adherence Screener index
    Description
    1. MEDAS (Mediterranean Diet Adherence Screener index). Scale of adherence to the Mediterranean diet of 14 items.
    Time Frame
    Change from Baseline Nutritional profile at 12 weeks
    Title
    Degree of frailty - Fried criteria
    Description
    The Fried frailty phenotype (FP) assesses physical frailty through five criteria: unintentional weight loss; weakness or poor handgrip strength; self-reported exhaustion; slow walking speed; and low physical activity.
    Time Frame
    Change from Baseline frailty degree at 12 weeks
    Title
    Body composition - Bioimpedance
    Description
    The body composition will be evaluated by means of bioimpedance.
    Time Frame
    Change from Baseline Bioimpedance composition at 12 weeks
    Title
    Body composition - body mass index (BMI)
    Description
    Weight and height will be combined to report BMI in kg/m^2
    Time Frame
    Change from Baseline body mass index (BMI) at 12 weeks
    Title
    Body composition - height
    Description
    Height measure in meter
    Time Frame
    Change from Baseline height at 12 weeks
    Title
    Body composition - weight
    Description
    Weight measure in kilograms
    Time Frame
    Change from Baseline weight at 12 weeks
    Title
    Musculoskeletal ultrasound architecture
    Description
    All ultrasound images will be acquired by the same operator with the same ultrasound device throughout the whole study using a linear 40 mm transducer and a phased array transductor, and images will be analysed through the ACSAuto script to semi-automatically evaluate ultrasound pictures. The vastus lateralis architecture will be analysed through the Simple Muscle Architecture Analysis tool for Fiji. These procedures will be done according to Rodriguez-López et al. Rodriguez-Lopez, C. et al. Effects of Power-Oriented Resistance Training With Heavy vs. Light Loads on Muscle-Tendon Function in Older Adults: A Study Protocol for a Randomized Controlled Trial. Front Physiol 12, (2021).
    Time Frame
    Change from Baseline Musculoskeletal ultrasound architecture at 12 weeks
    Title
    Depressive Symptoms
    Description
    The depressive symptoms will be assessed with the Geriatric Depression scale to assess psychology status of the participants.
    Time Frame
    Change from Baseline Depressive Symptoms at 12 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    70 Years
    Maximum Age & Unit of Time
    99 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Following the 2014 Consensus Document on the prevention of frailty and falls in the elderly patient we will recruit individuals I) > 70 years of age II) with a Barthel Index score > 75 III) meeting at least one of the following two criteria: a score ≤9 in the short physical performance battery (SPPB) or FRAIL questionnaire with values 1 or 2. Exclusion Criteria: I) Inability to go to the Primary Care Health Centre for any reason. II) Moderate to severe cognitive impairment (Mini-Mental State Examination< 20 points III) Severe pathology for which physical activity is contraindicated at the physician's discretion including but not limited to: recent acute myocardial infarction (6 months), uncontrolled cardiac arrhythmia, severe cardiac valve disease, non-controlled hypertension (> 180/100mmHg), non-controlled/severe heart failure, severe respiratory insufficiency disease, and diabetes mellitus with acute decompensation/frequent hypoglycaemia.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Alejandro Galan-Mercant, PhD
    Phone
    0034 667972031
    Email
    alejandro.galan@uca.es
    First Name & Middle Initial & Last Name or Official Title & Degree
    Daniel Velazquez-Diaz, PhD
    Phone
    0034 610035133
    Email
    daniel.velazquez@uca.es
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Alejandro Galan-Mercant, PhD
    Organizational Affiliation
    University of Cádiz
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    All data will be available in an open repository. RODIN is the Repository of Teaching and Research Objects of the University of Cádiz. It contributes to increased visibility of work developed, increases the impact and ensures the preservation of said production. All ethics aspects will be considered to ensure confidentiality of the data as detailed. The University of Cadiz has a new "hybrid cloud" infrastructure, made up of the University of Cadiz's own cloud, combined with others external providers. This service provides secure, efficient and reliable storage, which safeguards the necessary guarantees for autonomy, security and control over the data. Each researcher has an internal space of 500 GB, and an external cloud space of 250 GB. As for backup systems, the one offered by the UCA includes full copies of the space 3 times a week, while external providers have their own backup system, which allows restoring any accidentally deleted information up to 20 days after the incident.
    IPD Sharing URL
    https://rodin.uca.es/handle/10498/6086
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    Viability of an Educational Program for Lifestyle Changes and an Algorithm for the Derivation of Exercise Programs in Older People at Risk of Dependency at Primary Care.

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