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Vibrational-proprioceptive Resistance Exercise Training Versus Neuromuscular Electrical Stimulation Training in Elderly People With Muscle Weakness

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01679977
Acronym
MOBIL
Enrollment
150
Registered
2012-09-06
Start date
2008-06-30
Completion date
2015-03-31
Last updated
2016-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Weakness Condition, Therapy Effect

Brief summary

Study the structural behaviours of weak muscle of elderly and evaluate the efficiency of two different types of training.

Interventions

DEVICEVibrational-proprioceptive Resistance Exercise Training
DEVICENeuromuscular Electrical Stimulation Training

Sponsors

European Union
CollaboratorOTHER
Ministry of Science and Research, Austria
CollaboratorUNKNOWN
Medical University of Vienna
CollaboratorOTHER
Comenius University
CollaboratorOTHER
Ludwig Boltzmann Institute of Electrical Stimulation and Physical Rehabilitation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* age related muscle weakness * age between 65-85 years * all inclusion criterias must be fullfilled

Exclusion criteria

* recent hip or knee endp-prosthesis (within last 2 years), longstanding immobility * body mass index greater than 40 * acute thrombosis in lower extremity (within last 3 weeks) * severe articular effusion * acute infection * known myopathy * relevant neurological diseases with gait disorders (e.g. poly neuropathy, Parkinson's disease) * dementia, impaired cognitive abilities * diseases of the vestibular system causing vertigo or impairing balance * symptomatic cardio pulmonal diseases within the last 6 months * not or insufficient treated hypertonia * rheumatic diseases * other relevant functional impairment of the musculo-skeletal system caused by surgery, trauma or degenerative diseases * pain in the lower extremity (VAS \> 5) * if one of the above criteria applies the subject will be excluded from the study

Design outcomes

Primary

MeasureTime frame
Maximum voluntary knee extension torquepre Training, post Training, 3 months post training

Countries

Austria, Slovakia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026