Low-volume Cycling Training in Older People With Multimorbidity
Frailty, Morbidity, Multiple
About this trial
This is an interventional treatment trial for Frailty focused on measuring physical exercise, body composition, physical functionality, blood pressure, individualized training, morbidity
Eligibility Criteria
Inclusion criteria:
- men and women aged 65 and older
- users of a care setting-daycare patients or nursing home residents
- a score < 5 in the Global Deterioration Scale (GDS), from no cognitive decline to moderate cognitive decline.
Exclusion criteria:
- physical limitations or musculoskeletal injuries that could affect cycling training performance; physical exercise contraindicated by the physiotherapist and verified by the medical doctor according to the medical register of each participant
- heart failure with a functional class according to the New York Heart Association (NYHA) Classification of NYHA III and IV
- the presence of acute pain that does not allow exercise training
- recent acute myocardial infarction (in last 6 months) or unstable angina
- uncontrolled hypotension
- uncontrolled arterial hypertension (>180/100 mmHg)
- active cancer treatment with chemotherapy
- patients with an active pacemaker and/or uncontrolled block
- diabetes mellitus with acute decompensation or uncontrolled hypoglycemia
- any other circumstance that precludes individuals from completing the training intervention.
Sites / Locations
- Universidade da Coruña
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Experimental: Motorized cycle ergometer
Control group
The exercise group cycles 20 minutes per session on the MOTOmed Muvi 3 days per week for 6 weeks at an intensity guided by the perception of effort. A cycling cadence is fixed between 25 and 30 rpm for all sessions since that cadence is comfortable for every participant. Researchers adjust resistance on the motorized cycle to increase the external load until it reached the level required to reach the intensity of effort programmed by the OMNI-RPE. The six weeks are programmed in the form of two intensity-differentiated training phases of three weeks. In the first training phase (i.e., the first three weeks), participants are requested to cycle simultaneously with the upper and lower limbs at an intensity equivalent to a perception of 3 (i.e., easy to somewhat moderate) on the OMNI-RPE (0-10).
Participants are evaluated the week before and the week after the experimental group finishes the training period (pre- vs. postintervention) to facilitate an examination of the changes in body composition, functional performance, and resting cardiovascular state.