Frailty Clinical Trial
Official title:
A Multicomponent Physical Exercise Program: a Tool to Maintain Autonomy, Reduce Frailty and Improve Functionality in Nursing Homes. Interventional Single Group Study
Verified date | October 2023 |
Source | University of the Basque Country (UPV/EHU) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this research study is to determine whether a physical exercise program in nursing homes will maintain autonomy in activities of daily living, decrease vulnerability and improve physical, psychological and cognitive condition. An individualized and progressive multi-component physical exercise program focused on function has been designed to achieve this objective. Participant will engage in an exercise program for 6 months in their nursing homes, in two sessions per week of 45-60 minutes
Status | Completed |
Enrollment | 207 |
Est. completion date | December 31, 2020 |
Est. primary completion date | June 30, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 70 Years to 115 Years |
Eligibility | Inclusion Criteria: - Aged =70years - Scored =50 on the Barthel index - Scored =20 on Mini Examen Cognoscitive test (MEC-35), validated and adapted Spanish version of Mini Mental State Examination - Be able to stand up from the chair and walk 10 meters with or without one person/technical assistance. Exclusion Criteria: - If the participants are clinically unstable under the clinical judgment of the medical professionals of the reference center, - If the risk of adverse effects is greater than the benefit - If the participants have severe cognitive or psychiatric disorders. |
Country | Name | City | State |
---|---|---|---|
Spain | Basque Country University | Leioa | Bizkaia |
Lead Sponsor | Collaborator |
---|---|
University of the Basque Country (UPV/EHU) |
Spain,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Barthel Index | Autonomy on daily living activities will be analyzed using the Barthel index. The Barthel index is a questionnaire with 10 items that evaluates the autonomy of the participant in the activities of daily life and it will be evaluated with the reference caregiver in nursing home. The Barthel index evaluates the following items: Feeding, Bathing, Dressing, Grooming, Bowels, Bladder, Toilette use, Transfer, Walking and Stairs. This items are scored as follows: 0 points if it is totally dependent, 5 points if needs some help and 10 points if the participant is totally autonomous | Changes from baseline to 3rd 6th and 12th month | |
Primary | Short Physical Performance Battery | Short Physical Performance Battery (SPPB) evaluates balance, gait ability, and leg strength using a single tool. The score for each part is given in categorical modality (0-4). This set of tests serves to predict falls, weakness and mortality. The best score will be 12 points and total score less than 10 points indicates frailty and high risk of disability. 1 point of change in the total score has demonstrated to be of clinical relevance. | Changes from baseline to 3rd 6th and 12th month | |
Primary | Handgrip strength | To asses upper limbs strength (kg) will be used bilateral handgrip strength test by squeezing a dynamometer with maximum isometric effort for 5 seconds. It is a strong predictor of disability, morbidity, and mortality as well as one of the components of Fried's frailty phenotype. Ranges are corrected by BMI | Changes from baseline to 3rd 6th and 12th month | |
Primary | Timed Up and Go Test | Timed Up and Go (TUG) is a simple test used to assess a person's mobility and requires both static and dynamic balance. It uses the time that a person takes to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down. The cut-off value for the TUG is 12 seconds The test score also correlates well with gait speed and the Barthel Index. | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Fried frailty index | Fried index uses 5 criteria to define frailty: weight loss, exhaustion, physical activity, walk time and grip strength. Fulfilling three of these criteria indicates clinical frailty. | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Tilburg frailty indicator | Tilburg indicator evaluates frailty through a self-reported questionnaire that includes physical, psychological and social domains. The score range is from 0 points to 15 points. High scores indicates higher frailty | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Rockwood frailty phenotype | 9 phenotype ranging from very fit to terminally ill are evaluated in Rockwood frailty scale. | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Anthropometry-Weight | Weight (kg) | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Anthropometry-Height | Height (m) | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Body Mass Index | Body Mass Index (BMI), weight and height will be combined to report BMI in kg/m^2) | Changes from baseline to 3rd 6th and 12th month | |
Secondary | Anthropometry-Circumferences | Neck circumference, mid arm circumference and calf circumference (cm) | Changes from baseline to 3rd 6th and 12th month | |
Secondary | The Goldberg Anxiety and Depression Scale | The Goldberg Anxiety and Depression Scale will be used to assess affective state of anxiety and depression that includes nine depression and nine anxiety items from the last month. The cut-off points are =4 for the anxiety scale, and =2 for the depression scale. | Changes from baseline to 6th and 12th month | |
Secondary | The Spanish Subjective Happiness scale | The Spanish Subjective Happiness scale test will be used to analyze the perceived happiness. It ranges from 0 to 28 points in four questions. Higher punctuation means higher happiness level. | Changes from baseline to 6th and 12th month | |
Secondary | Quality of Life-Alzheimer Disease | Quality of Life-Alzheimer Disease (QoL-AD) test. Self-rated quality of life for people with cognitive impairments. The QoL-AD is comprised of 13 items (physical health, energy, mood, living situation, memory, family, marriage, friends, self as a whole, ability to do chores, ability to do things for fun, money and life as a whole). Response options include 1(poor), 2(fair), 3(good) and 4 (excellent), for a total score of 13-52, with higher scores indicating better QoL. | Changes from baseline to 6th and 12th month | |
Secondary | Montreal Cognitive Assessment test (MOCA test) | The cognitive function will be assessed by MOCA test. Montreal Cognitive Assessment cover domains: attention and concentration, executive functions, memory and language skills, conceptual thinking, calculation and orientation. The MOCA is a validated test in Spanish. It ranges from 0 ( worse score ) to 30 (best score). A score less than 26 indicates suggest mild cognitive decline | Changes from baseline to 6th and 12th month | |
Secondary | Pain level | Using a score from 0 points (lowest) to 10 points (highest) the participant will be asked to say how much it hurts in different parts of the body such as shoulders, elbows, wrists, neck, back, hips, knees and ankles | Changes from baseline to 6th and 12th month | |
Secondary | Clinical outcomes-Number of falls | Number of falls will be assessed with a clinical questionnaire | The data will be collected one year and 6 months before starting the project, at intervention baseline, at 6 months and at 12 months | |
Secondary | Clinical outcomes-visits to the emergency service | Visits to the emergency service will be assessed with a clinical questionnaire | The data will be collected one year and 6 months before starting the project, at intervention baseline, at 6 months and at 12 months | |
Secondary | Clinical outcomes-hospital admissions | Hospital admissions will be assessed with a clinical questionnaire | The data will be collected one year and 6 months before starting the project, at intervention baseline, at 6 months and at 12 months | |
Secondary | Clinical outcomes-functional impairment | Functional impairment after hospitalization will be assessed with a clinical questionnaire | The data will be collected one year and 6 months before starting the project, at intervention baseline, at 6 months and at 12 months |
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