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Exercise Program for Maintaining Physical Function and Frailty on Dwelling Older Adults (FragiCare)

Primary Purpose

Frailty

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Exercise
Recommendations for active lifestyle
Sponsored by
University of the Basque Country (UPV/EHU)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Frailty focused on measuring exercise, physical activity, funcionality, elderly, dwelling, socio-sanitary management

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: 70 years or older. Home care users managed by the municipal social network. In a stable situation (no worsening, no convalescence, no hospital discharge). Frail or pre-frail individuals. Exclusion Criteria: At the end of life. <60 on the Barthel Index. Cognitive impairment that affects their decision-making ability (Mini Mental State Examination, MMSE <24). Subjects that, on Home Care Service's assistant's criteria, do not meet the conditions to be included in the study.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Experimental

    Arm Label

    Control Group

    Intervention Group

    Arm Description

    The control group will receive general recommendations for maintaining physically active and reducing sedentary behaviors. This will be done verbally and through written material.

    The intervention group will receive the same recommendations as the control group. In addition, they will participate in a 6-month multicomponent physical exercise program consisting of a) 1 face-to-face weekly multicomponent session (Rodriguez-Larrad et al. BMC Geriatrics (2017) 17:60), and b) 2 autonomous sessions at home following the Vivifrail program (https://vivifrail.com/es/inicio/). Face-to-face supervised sessions will last 1 hour and include strength, balance, and flexibility exercises (50%-75% of the 1 repetition maximum for strength exercises). The volume, intensity and difficulty of the exercises will be individualized based on the initial performance of each participant, and will progress as the participants' physical capacity evolves. At-home training will follow the Vivifrail program.

    Outcomes

    Primary Outcome Measures

    Change from baseline Short Physical Performance Battery (SPPB) total score at 6 months
    The SPPB consists of three tasks that evaluate the lower extremities' function: balance, walking speed and sit-to-stand 5 times from a chair. In each task 0 to 4 points can be scored, to obtain a total score between 0 and 12 points. Higher values indicate better function.

    Secondary Outcome Measures

    Change from baseline Fried's frailty phenotype score at 6 months
    Frailty will be analyzed with the 5 criteria suggested by Fried: unintentional weight loss, weakness or poor handgrip strength, self-reported exhaustion, slow walking speed, and low physical activity. The presence of each criterion will be scored with one point, the total score ranging between 0-5 points. A higher score indicates higher frailty.
    Change from baseline height at 6 months
    Height will be measured and reported in meters, following ISAK's criteria.
    Change from baseline weight at 6 months
    Weight will be measured and reported in kilograms, following ISAK's criteria.
    Change from baseline hand grip at 6 months
    The grip strength of each hand will be measured with a manual dynamometer. This variable is related to the general strength of the subject, where higher values indicate greater strength.
    Change from baseline Eight Foot up and Go (8-FUG) at 6 months
    The test measures the time the subject needs to stand from a chair, walk 8 feet (2,5 meters), turn around, get back to the chair, and sit. The longer the time to complete the test, the worse the performance. Leaning on the thighs or the chair is allowed to stand.
    Change from baseline Nutritional state at 6 months
    The nutritional state will be evaluated using the short form (SF) of the Mini-Nutritional Assessment (MNA). The score of SF-MNA oscillates between 0 and 14. The nutritional state can be classified as normal nutrition (12 to 14 points), potential risk of malnutrition (8 to 11 points), and malnutrition (<7 points).
    Change from baseline Cognition at 6 months
    The Montreal Cognitive Assessment will be used to evaluate the cognitive function of participants. It analyzes the following abilities: attention, concentration, executive functions (including abstraction ability), memory, language, visual-construction-related abilities, calculus, and orientation. The maximum score is 30 points; a score of 26 or higher is considered normal.
    Change from baseline Anxiety and Depression at 6 months
    Anxiety and Depression Goldberg Scale. The scale is formed of two subscales with nine questions each: the anxiety subscale and the depression subscale. The total score in both subscales goes from 0 to 9, since each question scores 1 point if the answer is affirmative, and 0 points if it is not. In the anxiety subscale, the cut-off point which determines that the participant has a risk of suffering anxiety is 4 points or more, and the depression risk is 2 points or more. In both subscales the higher the score, the higher the risk.
    Change from baseline health-related quality of life at 6 months
    European Quality of Life-5 Dimensions (EQ-5D) questionnaire. Participants will self-rate their health on a vertical visual analogue scale (score range: 0-100), where the endpoints are labeled 'The worst health you can imagine' and 'The best health you can imagine'. Higher values indicate better quality of life.
    Change from baseline Meaning in Life Questionnaire score at 6 months
    The Spanish version of the Meaning in Life Questionnaire will be used. It contains 10 questions that evaluate the meaning of life. The questionnaire has Likert-type options which go from "absolutely false", which scores 1 point, to "absolutely true", which scores 7 points. The total score goes from 10 to 70 points. Higher scores indicate better values.
    Change from baseline Satisfaction With Life Scale score at 6 months
    It is a 5-question scale with Likert-type answers of 5 categories that examines de global grade of satisfaction with life. Possible answers go from absolutely untrue (1) to absolutely true (5). A score of 5 to 25 points can be obtained. Higher values indicate better satisfaction with life.
    Change from baseline Subjective Happiness Scale score at 6 months
    The scale consists of 4 questions. The first three questions include 7 possible Likert-type answers, where the minimum score is 1 (little happy) and the maximum is 7 (totally happy). In the last question, the Likert scale is modified, where the minimum score is 1 (not at all) and the maximum is 7 (a great deal). The maximum score possible is 28 points. Higher values indicate a better score.
    Sociodemographic information
    Date of birth, sex, place of residence, cohabitation model and social network. Any change in those circumstances will be recorded from baseline assessment up to 6 months.
    Number of falls
    The number of falls each participant will suffer during the program will be recorded on a self-reported basis and from Home Care Service's registers. It will also include the number of falls in the last 6 months from the Home Care Service's registers. This will be prospectively recorded from the date of baseline assessment until the date of the first documented fall, assessed up to 6 months.
    Attendance to the face-to-face exercise sessions
    The number of face-to-face sessions carried out by each participant will be prospectively collected by the trainer in each session.
    Attendance to the autonomous sessions at home
    The number of completed autonomous sessions at home will be self-reported. Participants will prospectively register them on a sheet, which will be delivered weekly to the trainer during the program.
    Alarms to the social and health care services
    Professionals in charge of the home care service provided to the dwelling older adults will collect data in a digital platform regarding the health and social conditions of the person they care for. In the event of a significant change in the conditions that affect the older adults (fall, reduction in functional level, modification of the nutritional pattern, change in the social network, ...), the platform generates a series of alarms. These alarms are then referred to the older adult health and/or social care professionals. We will assess the number of alarms referred to the health and/or social care professionals of the participants.

    Full Information

    First Posted
    January 25, 2023
    Last Updated
    March 19, 2023
    Sponsor
    University of the Basque Country (UPV/EHU)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05726214
    Brief Title
    Exercise Program for Maintaining Physical Function and Frailty on Dwelling Older Adults
    Acronym
    FragiCare
    Official Title
    Effectiveness of the Fragicare Exercise Program on Functional and Socio-sanitary Management Parameters
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    March 2023 (Anticipated)
    Primary Completion Date
    December 2023 (Anticipated)
    Study Completion Date
    March 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of the Basque Country (UPV/EHU)

    4. Oversight

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

    5. Study Description

    Brief Summary
    Older people living in their homes and receiving social assistance are at a high risk of suffering functional loss, hospitalization and/or developing disability. This condition is known as frailty. Exercise programs including strength, balance and flexibility training have demonstrated to prevent, delay or even treat frailty. However, participation in this type of exercise programs is very limited in the group of older adults mentioned above. The present study seeks to evaluate the effects of an exercise program designed to maintain or improve physical function and frailty. The hypothesis is that people who participate in the physical exercise program will maintain or improve their physical capacity, their frailty and psycho-affective status, their quality of life, and generate a lower demand for social and health services compared to those people who do not exercise.
    Detailed Description
    Frailty is recognized as a syndrome that encompasses a high risk of suffering functional loss, hospitalization and/or developing dependency, among other adverse health events. It is considered a modifiable factor, capable of being reversed if intervention is made in the early stages of its development. The implementation of multicomponent physical exercise programs has been proven to prevent, delay or even treat frailty. However, participation in this type of exercise programs is very limited in older people living in their homes and receiving social assistance. Social assistance in Spain is recognized as a care and preventive nature service intended to help older adults in a situation of dependency, or risk of dependency, to remain at their homes, offering them the required domestic and personalized assistance that enables their development in their own homes and their integration into the community environment, avoiding situations of isolation. Older people living in their homes and receiving social assistance population is characterized by being particularly vulnerable, since it presents high rates of frail people that are in the initial stages of dependency, which makes them a target to significantly benefit from the effects of exercise. The approach to tackling frailty has become a Public Health priority at a European, state and regional level, as it affects both the health and social systems in an increasingly aging society. Nevertheless, there are currently no frailty management models in an integrated manner between health and social service systems. In this context arises the FRAGICARE project, which aspires to develop a model of shared health and social management, sustainable in the long term, which promotes the permanence of the older adults in their usual social environment, respecting their lifestyles and preferences. This model is supported by a digital platform uploaded in the cellular, fed by the data collected by the professionals who are in charge of the home care service provided to the dwelling older adults. In the event of a significant change in the conditions that affect these older adults (fall, reduction in functional level, modification of the nutritional pattern, change in the social network, ...), the platform generates a series of alarms that are referred to their healthcare and/or social professional, who will reassess and, if necessary, adjust the care plan. These alarms have been defined by a multidisciplinary group of experts and piloted in a previous project. In this way, the model seeks to provide individualized, continuous and coordinated care between the basic social services system and the health system (primary and specialized care services). The objective of the present study is to assess the effects of a physical exercise program from a multidimensional perspective, including physical function, frailty status, psycho-affective parameters, and quality of life. In addition, we will also evaluate the effect of the program in the number of alarms generated by the digital platform to the social and health services. The hypothesis is that people who participate in the physical exercise program will maintain or improve their physical function, their frailty status, psycho-affective capacity, quality of life, and generate a lower number of social and health services alarms compared to those people who do not exercise.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Frailty
    Keywords
    exercise, physical activity, funcionality, elderly, dwelling, socio-sanitary management

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomized controlled pilot study
    Masking
    Care ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Control Group
    Arm Type
    Other
    Arm Description
    The control group will receive general recommendations for maintaining physically active and reducing sedentary behaviors. This will be done verbally and through written material.
    Arm Title
    Intervention Group
    Arm Type
    Experimental
    Arm Description
    The intervention group will receive the same recommendations as the control group. In addition, they will participate in a 6-month multicomponent physical exercise program consisting of a) 1 face-to-face weekly multicomponent session (Rodriguez-Larrad et al. BMC Geriatrics (2017) 17:60), and b) 2 autonomous sessions at home following the Vivifrail program (https://vivifrail.com/es/inicio/). Face-to-face supervised sessions will last 1 hour and include strength, balance, and flexibility exercises (50%-75% of the 1 repetition maximum for strength exercises). The volume, intensity and difficulty of the exercises will be individualized based on the initial performance of each participant, and will progress as the participants' physical capacity evolves. At-home training will follow the Vivifrail program.
    Intervention Type
    Other
    Intervention Name(s)
    Exercise
    Intervention Description
    The face-to-face multicomponent program will entail: Strength training of upper and lower limbs. Familiarization phase will include 2-3 exercises of 1-2 series and 8-12 repetitions per session. During the acquisition phase, 2-3 exercises of 2-3 series and 8-12 repetitions at a higher velocity. The resting time between sets will be of 1-3 minutes. Balance exercises will include proprioception, agility and weight transfer exercises. Difficulty will progressively increase by reducing the base of support, by including multidirectional displacements, walking on tiptoe or heels, body-weight transfer, dynamic exercises modifying the centre of gravity, and stressing postural muscles and by sensorial reductions. Flexibility exercises: Static stretching maintained during 20-30s carried out at the end of each session. The Vivifrail exercise wheel corresponding to each participant will be given according to their functional level type.
    Intervention Type
    Other
    Intervention Name(s)
    Recommendations for active lifestyle
    Intervention Description
    After the baseline assessments, all participants will receive individualized counseling for following physically active lifestyle and reducing sedentary behaviors. Participants will be encouraged to increase the physical activity time and intensity, and to hourly break the sedentary time while at home. The recommendations will be transmitted verbally and through written material.
    Primary Outcome Measure Information:
    Title
    Change from baseline Short Physical Performance Battery (SPPB) total score at 6 months
    Description
    The SPPB consists of three tasks that evaluate the lower extremities' function: balance, walking speed and sit-to-stand 5 times from a chair. In each task 0 to 4 points can be scored, to obtain a total score between 0 and 12 points. Higher values indicate better function.
    Time Frame
    Baseline and 6 months
    Secondary Outcome Measure Information:
    Title
    Change from baseline Fried's frailty phenotype score at 6 months
    Description
    Frailty will be analyzed with the 5 criteria suggested by Fried: unintentional weight loss, weakness or poor handgrip strength, self-reported exhaustion, slow walking speed, and low physical activity. The presence of each criterion will be scored with one point, the total score ranging between 0-5 points. A higher score indicates higher frailty.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline height at 6 months
    Description
    Height will be measured and reported in meters, following ISAK's criteria.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline weight at 6 months
    Description
    Weight will be measured and reported in kilograms, following ISAK's criteria.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline hand grip at 6 months
    Description
    The grip strength of each hand will be measured with a manual dynamometer. This variable is related to the general strength of the subject, where higher values indicate greater strength.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Eight Foot up and Go (8-FUG) at 6 months
    Description
    The test measures the time the subject needs to stand from a chair, walk 8 feet (2,5 meters), turn around, get back to the chair, and sit. The longer the time to complete the test, the worse the performance. Leaning on the thighs or the chair is allowed to stand.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Nutritional state at 6 months
    Description
    The nutritional state will be evaluated using the short form (SF) of the Mini-Nutritional Assessment (MNA). The score of SF-MNA oscillates between 0 and 14. The nutritional state can be classified as normal nutrition (12 to 14 points), potential risk of malnutrition (8 to 11 points), and malnutrition (<7 points).
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Cognition at 6 months
    Description
    The Montreal Cognitive Assessment will be used to evaluate the cognitive function of participants. It analyzes the following abilities: attention, concentration, executive functions (including abstraction ability), memory, language, visual-construction-related abilities, calculus, and orientation. The maximum score is 30 points; a score of 26 or higher is considered normal.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Anxiety and Depression at 6 months
    Description
    Anxiety and Depression Goldberg Scale. The scale is formed of two subscales with nine questions each: the anxiety subscale and the depression subscale. The total score in both subscales goes from 0 to 9, since each question scores 1 point if the answer is affirmative, and 0 points if it is not. In the anxiety subscale, the cut-off point which determines that the participant has a risk of suffering anxiety is 4 points or more, and the depression risk is 2 points or more. In both subscales the higher the score, the higher the risk.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline health-related quality of life at 6 months
    Description
    European Quality of Life-5 Dimensions (EQ-5D) questionnaire. Participants will self-rate their health on a vertical visual analogue scale (score range: 0-100), where the endpoints are labeled 'The worst health you can imagine' and 'The best health you can imagine'. Higher values indicate better quality of life.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Meaning in Life Questionnaire score at 6 months
    Description
    The Spanish version of the Meaning in Life Questionnaire will be used. It contains 10 questions that evaluate the meaning of life. The questionnaire has Likert-type options which go from "absolutely false", which scores 1 point, to "absolutely true", which scores 7 points. The total score goes from 10 to 70 points. Higher scores indicate better values.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Satisfaction With Life Scale score at 6 months
    Description
    It is a 5-question scale with Likert-type answers of 5 categories that examines de global grade of satisfaction with life. Possible answers go from absolutely untrue (1) to absolutely true (5). A score of 5 to 25 points can be obtained. Higher values indicate better satisfaction with life.
    Time Frame
    Baseline and 6 months
    Title
    Change from baseline Subjective Happiness Scale score at 6 months
    Description
    The scale consists of 4 questions. The first three questions include 7 possible Likert-type answers, where the minimum score is 1 (little happy) and the maximum is 7 (totally happy). In the last question, the Likert scale is modified, where the minimum score is 1 (not at all) and the maximum is 7 (a great deal). The maximum score possible is 28 points. Higher values indicate a better score.
    Time Frame
    Baseline and 6 months
    Title
    Sociodemographic information
    Description
    Date of birth, sex, place of residence, cohabitation model and social network. Any change in those circumstances will be recorded from baseline assessment up to 6 months.
    Time Frame
    Baseline and in any moment that any of them might change (place of residence, cohabitation model and social network) up to 6 months.
    Title
    Number of falls
    Description
    The number of falls each participant will suffer during the program will be recorded on a self-reported basis and from Home Care Service's registers. It will also include the number of falls in the last 6 months from the Home Care Service's registers. This will be prospectively recorded from the date of baseline assessment until the date of the first documented fall, assessed up to 6 months.
    Time Frame
    From baseline assessment up to 6 months
    Title
    Attendance to the face-to-face exercise sessions
    Description
    The number of face-to-face sessions carried out by each participant will be prospectively collected by the trainer in each session.
    Time Frame
    From the first session up to the last one during the 6 months
    Title
    Attendance to the autonomous sessions at home
    Description
    The number of completed autonomous sessions at home will be self-reported. Participants will prospectively register them on a sheet, which will be delivered weekly to the trainer during the program.
    Time Frame
    From the first session up to the last one during the 6 months
    Title
    Alarms to the social and health care services
    Description
    Professionals in charge of the home care service provided to the dwelling older adults will collect data in a digital platform regarding the health and social conditions of the person they care for. In the event of a significant change in the conditions that affect the older adults (fall, reduction in functional level, modification of the nutritional pattern, change in the social network, ...), the platform generates a series of alarms. These alarms are then referred to the older adult health and/or social care professionals. We will assess the number of alarms referred to the health and/or social care professionals of the participants.
    Time Frame
    Daily from baseline assessment up to 6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 70 years or older. Home care users managed by the municipal social network. In a stable situation (no worsening, no convalescence, no hospital discharge). Frail or pre-frail individuals. Exclusion Criteria: At the end of life. <60 on the Barthel Index. Cognitive impairment that affects their decision-making ability (Mini Mental State Examination, MMSE <24). Subjects that, on Home Care Service's assistant's criteria, do not meet the conditions to be included in the study.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Ana AR Rodriguez Larrad
    Phone
    +34 946 01 79 25
    Email
    ana.rodriguez@ehu.eus
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jon JI Irazusta
    Phone
    +34 946 01 2837
    Email
    jon.irazusta@ehu.eus
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ana AR Rodriguez Larrad
    Organizational Affiliation
    UPV/EHU
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    Data will be shared under reasonable demand
    IPD Sharing Time Frame
    When data will be collected and analyzed
    IPD Sharing Access Criteria
    Data will be shared under reasonable demand to the principal investigator
    Citations:
    PubMed Identifier
    11253156
    Citation
    Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, Seeman T, Tracy R, Kop WJ, Burke G, McBurnie MA; Cardiovascular Health Study Collaborative Research Group. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. 2001 Mar;56(3):M146-56. doi: 10.1093/gerona/56.3.m146.
    Results Reference
    background
    Citation
    Stewart A, Marfell-Jones M, International Society for Advancement of Kinanthropometry. International Standards for Anthropometric Assessment. ISAK, 2011
    Results Reference
    background
    Citation
    Mayordomo MM. Análisis Dinamométrico de la Mano: Valores Normativos en la Población Española. Madrid: Universidad Complutense de Madrid, Servicio de Publicaciones,; 2011
    Results Reference
    background
    Citation
    Rikli, R.E., Jones, C.J., 2001. Senior Fitness Test. Champaign: Human Kinetics. (ISBN 0-7360-3356-3364
    Results Reference
    background
    PubMed Identifier
    19812868
    Citation
    Kaiser MJ, Bauer JM, Ramsch C, Uter W, Guigoz Y, Cederholm T, Thomas DR, Anthony P, Charlton KE, Maggio M, Tsai AC, Grathwohl D, Vellas B, Sieber CC; MNA-International Group. Validation of the Mini Nutritional Assessment short-form (MNA-SF): a practical tool for identification of nutritional status. J Nutr Health Aging. 2009 Nov;13(9):782-8. doi: 10.1007/s12603-009-0214-7.
    Results Reference
    background
    PubMed Identifier
    15817019
    Citation
    Nasreddine ZS, Phillips NA, Bedirian V, Charbonneau S, Whitehead V, Collin I, Cummings JL, Chertkow H. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005 Apr;53(4):695-9. doi: 10.1111/j.1532-5415.2005.53221.x. Erratum In: J Am Geriatr Soc. 2019 Sep;67(9):1991.
    Results Reference
    background
    PubMed Identifier
    3140969
    Citation
    Goldberg D, Bridges K, Duncan-Jones P, Grayson D. Detecting anxiety and depression in general medical settings. BMJ. 1988 Oct 8;297(6653):897-9. doi: 10.1136/bmj.297.6653.897.
    Results Reference
    background
    Citation
    Steger MF, Frazier P, Kaler M, Oishi S. The meaning in life questionnaire: Assessing the presence of and search for meaning in life. J Couns Psychol. 2006;53(1):80-93
    Results Reference
    background
    PubMed Identifier
    16367493
    Citation
    Diener E, Emmons RA, Larsen RJ, Griffin S. The Satisfaction With Life Scale. J Pers Assess. 1985 Feb;49(1):71-5. doi: 10.1207/s15327752jpa4901_13.
    Results Reference
    background
    Citation
    Extremera N, Fernández-Berrocal P. The Subjective Happiness Scale: Translation and Preliminary Psychometric Evaluation of a Spanish Version. Soc Indic Res. 2014;119:473-481.
    Results Reference
    background

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    Exercise Program for Maintaining Physical Function and Frailty on Dwelling Older Adults

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