The objective of this study is to obtain insight in the characteristics of sarcopenic versus non-sarcopenic community-dwelling older people.
ID
Source
Brief title
Condition
- Muscle disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Characteristics (nutritional status, physical activity) of sarcopenic versus
non-sarcopenic community-dwelling older people.
Secondary outcome
Prevalence of sarcopenia, falls, frailty, activities of daily living, quality
of life, care use (health care costs).
Background summary
Sarcopenia is an age-related decline in muscle mass, strength and physical
performance, and is recognized as a geriatric syndrome. Sarcopenia by itself or
as a major component of frailty is associated with a risk of adverse outcomes
e.g. physical disability, increased risk of falls and fractures, poor quality
of life, loss of autonomy and independence, and death. Depending on the
diagnostic criteria, it is estimated that the prevalence of sarcopenia in
community-dwelling people above the age of 60 years varies between 10 and 50%.
As sarcopenia is relatively prevalent and because it increases the risk of
disability and the use of healthcare resources and institutionalization, the
economic burden for the healthcare system is great. Considerable evidence
suggests that sarcopenia is a partially reversible cause of disability and can
benefit from intervention, particularly at its early stages.
Study objective
The objective of this study is to obtain insight in the characteristics of
sarcopenic versus non-sarcopenic community-dwelling older people.
Study design
This study will be a cross-sectional study in the following settings:
community-dwelling persons (n=252), including people living at home without
home care, with home care, in an assisted living facility or in a home for
older people. Inclusion will last 1,5 year, or in case the preferred number of
participants is met, shorter. There is one measurement moment and measurements
will take place at the participant*s home.
During the home visit demographic data of participants will be collected. This
includes age, gender, ethnicity, living situation, presence of chronic
diseases, smoking, falls, BMI (height and weight) and cognitive function
(Mini-Mental State Examination, MMSE; Kok & Verhey, 2002). Co-morbidity will
not be an exclusion criterion per se, but participants with acute and/or
uncontrolled conditions, judged by the investigator, will be excluded.
Identification of sarcopenia will be done by measuring muscle mass, strength
and physical performance, by respectively an bioelectrical impedance analyzer ,
hand-held dynamometer and the Short Physical Performance Battery (including a
balance test, gait speed over a four meter course and by five chair stands).
Nutritional status will be assessed by a food frequency questionnaire, the Mini
Nutritional Assessment tool and a blood sample. Other questionnaires used are:
Minnesota Leisure Time Physical Activity Questionnaire (level of physical
activity), FRAIL scale and Fried criteria (physical frailty), GARS (activities
of daily living), EQ-5D-5L (quality of life) and health care use (developed in
cooperation with a professor in the field of Health Economics and HTA/economic
evaluation).
Study burden and risks
In this study, serious adverse events are unlikely, since previous studies
using the same battery of instruments have reported no or only few events
(mainly muscle soreness). Most of the individual tests are used in clinical
practice already.
Duboisdomein 30
Maastricht 6229GT
NL
Duboisdomein 30
Maastricht 6229GT
NL
Listed location countries
Age
Inclusion criteria
Subjects must meet all of the following criteria: * 65 years old, have given informed consent, understand Dutch language and are able to perform a walk test. Subjects from both sexes will be included.
Exclusion criteria
Older people living in a nursing home, older people with active rheumatoid arthritis, post stroke status with evident lingering symptoms (paralysis, loss of motor functions), diseases of the nervous system like Parkinson and MS, active angina pectoris, dementia, older people in a wheelchair, with ICD or pacemaker and subjects unable to perform the tests, as judged by the investigator.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
ClinicalTrials.gov | NCT01820988 |
CCMO | NL42626.068.13 |