Investigating My Active and Healthy Aging (my-AHA)
Frail Elderly Syndrome, Cognitive Impairment, Physical Dependence
About this trial
This is an interventional prevention trial for Frail Elderly Syndrome focused on measuring Frailty, Physical impairment, Cognitive decline, ICT
Eligibility Criteria
INCLUSION CRITERIA for pre-screening
- Age: over 60 yrs
- Able to stand and walk unassisted
- Free of significant cognitive impairment (age-corrected Mini Mental State Examination Test ≥ 24)
- Free of clinically significant mood disturbance (HADS-Anxiety <15; HADS-depression < 15)
- Free of any acute or unstable medical conditions
- Able to understand directions and participate in the protocol
- Able to sign informed consent
Subjects will be enrolled in the study if they meet one or two of the Fried et al. (2001) criteria for Frailty (Pre-Frailty status).
1. Shrinking, evidenced by weight loss (unintentional) ≥ 4.5 kg unintentional in prior 12 months; or at follow-up assessment ≥ 5% of body weight in prior 12 months.
2, Weakness. Grip strength in lowest 20% at baseline adjusted for gender and BMI.
3. Poor endurance and energy. Self-report of exhaustion as indicated by responses to 2 questions on Center for Epidemiologic Studies Depression (CES-D) scale.
4. Slowness .Time to walk 15ft (4.57m) ≤ slowest 20% adjusted for gender and standing height.
5. Low physical activity level. Lowest quintile (25%) by gender for weighted kcal expenditure per week at baseline.
EXCLUSION CRITERIA
Participant excluded if meets 1 or more of below:
Mobility problems
- cannot stand and ambulate unassisted
- painful arthritis, spinal stenosis, amputation, or painful foot lesions that limits balance and mobility,
Concurrent chronic disease independently contributing to frailty
suffers from a significant neurodegenerative disorder, e.g.
- Alzheimer's disease
- Lewy body dementia
- Frontotemporal Lobar Degeneration, Fronto-Temporal Dementia
- Parkinson's disease
- multiple sclerosis
- progressive supranuclear palsy
- amyotrophic lateral sclerosis
- hydrocephalus
- Huntington's disease
- prion diseases
affected by severe peripheral nervous system and/or neuromuscular disorders, e.g.
- chronic inflammatory demyelinating polyneuropathy
- myasthenia gravis
- multiple sclerosis
- polymyositis
Concomitant injury or disease known
- clinical evidence or history of stroke (within 2 yrs) to impact independently cognitive,
- clinical evidence or history of transient ischemic attack (within 6 months) psychological or physical function
- significant head injury with associated loss of consciousness, skull fracture or persisting cognitive impairment (2 years)
- epilepsy (a single prior seizure is considered acceptable)
if meet Diagnostic and Statistical Manual 5 (DSM-5) criteria for:
- major depressive disorder (current)
- schizophrenia or other psychotic disorders (lifetime)
- bipolar disorder (within the past 5 years
- substance (including alcohol) related disorders (within the past 2 years)
Presence of cognitive, sensory or
- have language deficits that impair testing perceptual deficits that interfere with assessment tasks
- have significant visual impairment
- have a significant hearing loss
Presence of other conditions or diseases that will compromise ability to undertake interventions (especially physical)
have clinically significant cardiovascular disease, i.e:
- hospitalization for acute coronary syndrome (acute myocardial infarction or unstable, angina)
- symptoms consistent with angina pectoris, within the 12 months
- signs or symptoms of clinical heart failure within the 12 months
- evidence of uncontrolled atrial fibrillation
- a cardiac pacemaker
preexisting or current signs or symptoms of respiratory failure, e.g.
- chronic obstructive pulmonary disease
- bronchial asthma
- lung fibrosis
- other respiratory disease
- untreated hypertension
- metastatic cancer or immunosuppressive therapy
- concurrent acute or chronic clinically significant immunologic, hepatic (such as presence of encephalopathy or ascites), or endocrine disease (not adequately treated).
Unacceptable Test/Laboratory Values
1. Postural hypotension (fall in systolic blood pressure of greater than 30 mmHg or fall in diastolic blood pressure of greater than 20 mmHg on standing compared to sitting) at the time of screening. Subjects who present at the time of screening with postural hypotension yet have no known history of postural hypotension, nor underlying medical condition related to hypotension, may be rescreened
Sites / Locations
- Aging Brain and Memory Clinic, Department of Neuroscience, University of TorinoRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Cases
Controls
Pre-frail subjects will use an ICT platform (my-AHA platform) embedded in a mobile phone and a fit-band that will continuously monitor physical and cognitive activities. Interventions regarding physical, cognitive, psychological and social domains will be prescribed and monitored through the my-AHA platform. In addition, sleep and dietary habits will be investigated and tailored interventions will be suggested.
Pre-frail subjects will be followed according to "best standard of care" protocols. Interventions regarding physical, cognitive, psychological and social domains will be prescribed. In addition, sleep and dietary habits will be investigated and tailored interventions will be suggested.