Reducing Falls With RENEW in Older Adults Who Have Fallen
Muscle Atrophy, Physical Deconditioning
About this trial
This is an interventional prevention trial for Muscle Atrophy focused on measuring Falling risk, muscle conditioning, muscle size, isometric strength, Incidence in falls
Eligibility Criteria
Inclusion Criteria:
- male or a female at least 65 years of age or older with 2 or more self-reported co-morbid conditions.
- experienced at least 1 fall (defined for this study as unintentionally coming to rest on the ground, floor, or other lower level) in the previous 12 months
- ambulatory, community dwelling with gait speed ranging from of 25m/min to 80m/min
- medically cleared by their physician to participate in a 60 minute (with rests) MCERFP
- capable of performing RENEW on the ergometer (see below)
- recall of all 3 items (or 1-2 items with a normal clock drawing test) on the Mini-Cog instrument for dementia
Exclusion Criteria:
- progressive diagnosed neurologic disease (e.g., Parkinson's, multiple sclerosis, Guillain-Barre, Alzheimers)
- any dystrophies or rheumatologic conditions that primarily affects muscle (muscular dystrophy, PMR)
- having already participated in a MCEFRP
- regular (3x/week) aerobic or resistance exercise performed over the past 12 months; "aerobic" defined as hiking, fast-walking, jogging, running swimming or cycling; "resistance" defined as weight training with bands, cable, free-weights or weight-machines
- Any of the following list of absolute contraindications for MRI:
- Cardiac Pacemakers (except in rare, controlled environments)
- Cochlear (inner ear) implants
- Swan-Ganz catheters with thermodilution tips
- Ferromagnetic or unidentifiable aneurysm clips of the brain
- Implanted neuro stimulators
- Metal or unidentifiable foreign bodies in the eyes
- Shrapnel near a vital organ
- Extreme claustrophobia
Sites / Locations
- Department of Physical Therapy, University of Utah
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
RENEW
TRADITIONAL
RENEW will occur on a recumbent ergometer that appears like a normal stepper ergometer. While resisting the foot pedal movement the participant experiences eccentric muscle contractions about the knee and hip while performing negative work. The progression of the 3 x/week (every other day), 12 week RENEW program will be determined as a function of the rating of perceived exertion (RPE) using a "target" workload on the monitor. RENEW will be increased very slowly over the first 3 weeks and, subsequently, to maintain an 11-13 perceived exertion. During the formal RENEW training regimen the participants become fully acclimated to the device (week 3-4) the total RENEW load will increase weekly with no increase in their RPE.
The TRAD group will perform their lower extremity resistance exercise for 15 minutes per session with isotonic weight machines and cuff weights as part of their multicomponent exercise fall reduction program (MCERFP). The progression of the 3 x/week, 12 week TRAD program will be determined as a relative function of their 1 repetition maximum (1RM) weight that can be lifted in a safe and successful manner. The 1RM will be measured before the 12 week training program and every 2 weeks thereafter. A "target" resistance workload (i.e., weight level) commensurate with 60-70% of the 1RM of the knee and hip extensors will be calculated bi-monthly and 3 sets of 15 repetitions of 3-4 different knee and hip exercises will be used over a 15 minute time period.