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Effects of Neuromuscular Electrostimulation (NMES) on physical function and skeletal muscle mass in acutely ill hospitalized geriatric patients with sarcopenia admiitted to an acute care geriatric hospital ward

NMES in sarcopenic acutely ill hospitalized geriatric patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23883
Enrollment
60
Registered
2020-03-11
Start date
2020-03-22
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Sarcopenia should be present. Patients are however admitted to the geriatric ward because of multiple problems mostly acute

Interventions

The patients in the control group (CG) will get usual care with daily physical therapy and the patients in the intervention group (IG) will get on top NMES during 5 days on working weekdays during 60

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a patient must meet all of the following criteria: aged 70 years and older, being frail according the Groningen Frailty Indicator (GFI score >3) and they should be sarcopenic according the European Working Group On Sarcopenia-2 criteria (EWGSOP-2) based on handgrip strength (men < 27kg and women < 16kg)), appendicular skeletal muscle mass (men < 7.0 kg/l2 and women < 7.0 kg/l2) and physical function below cut-off values (Short Physical Performance Battery <9). In a study done by Sipers et all in this population 92% of the men and 67% of the women were sarcopenic.3 Inclusion and first measurement should be done within the first three days after hospitalization.

Exclusion criteria

Exclusion criteria: A potential patient will be excluded from participation in this study if he/she meets any of the following criteria: Inability to walk prior index disease or problem before hospitalization. If a patient has a terminal condition e.g. due to metastatic cancer with a limited survival time (less than 3 month). Inability to walk due to pain or palsy during hospital stay. If a patient is not instruct able. If a patient has an implantable cardioverter defibrillator (ICD) or no informed consent.

Design outcomes

Primary

MeasureTime frame
To study the effects of NMES on top of exercise training on physical function and skeletal muscle mass in acutely ill sarcopenic hospitalized geriatric patients. Effects will be measured with the timed Chair Stand Test (t-CST), knee extension force (KEF) assessed with a handheld dynamometer ( MicroFet-2) and skeletal muscle mass of the upper leg (ul-SMM) with multifrequency bio-impedance analysis (mf-BIA). The difference in percentage of patients with changes on these parameters (t-CST, KEF and ul-SMM) in the IG compared to the patients in the CG.

Secondary

MeasureTime frame
To study the effect of NMES on improvement of mobility assessed with the short physical performance battery (SPPB) and the occurrence of possible adverse events. The difference in percentage of patients with changes on these parameters in the IG compared to the patients in the CG.

Contacts

Public ContactWalther Sipers

Zuyderland Medisch Centrum

w.sipers@zuyderland.nl06-20807691

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)