The main objective of this study is to investigate whether changes in nutritional status correlate to changes in frailty status, and whether these changes impact on disability as a clinical outcome in patients with chronic obstructive pulmonary…
ID
Source
Brief title
Condition
- Other condition
- Appetite and general nutritional disorders
Synonym
Health condition
ondervoeding, kwetsbaarheid en invaliditeit
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Disease-related malnutrition, frailty and disability
Secondary outcome
Dietary intake and requirement, physical activity, body composition, physical
functioning, clinical outcome
Background summary
Frailty is considered to be a clinical state in which there is an increase in
an individual*s vulnerability for developing increased dependency and/or
mortality when exposed to a stressor (Morley, Vellas et al. 2013). Frailty is a
strong predictor for the adverse clinical outcome of disability. This is an
individual problem, but also very relevant to society; people are getting older
but not necessarily in an independent and healthy way. The complex interactions
between factors of the multidimensional and dynamic concept of frailty remain
to be clarified (de Vries, Staal et al. 2011).
Since malnutrition has such an impact on physical performance, frailty and
malnutrition are suspected to correlate firmly. Knowing in what way these
conditions influence each other is extremely important in achieving to revolve
the process of becoming frail and disable.
Study objective
The main objective of this study is to investigate whether changes in
nutritional status correlate to changes in frailty status, and whether these
changes impact on disability as a clinical outcome in patients with chronic
obstructive pulmonary disease. The secondary objective is to explore adaptive
strategies for dietary challenges in chronically ill patients, and thus
predictors of dietary resilience, and dietary resiliency subsequently.
Study design
For this study (quantitative and qualitative research), an exploratory
longitudinal study design is used.
Study burden and risks
Patients will be assessed during rehabilitation at the UMCG-rehabilitation
center. In this longitudinal design, patients will be assessed 3 times during
their rehabilitation and 4 times in follow-up setting.
The following tests and questionnaires will be used: body weight, length,
accelerometer, mid upper arm circumference and triceps skinfold, bio-electrical
impedance analysis (including vector analysis), muscle ultrasound scan,
handgrip strength, gait speed, Short Physical Performance Battery, muscle tone,
PG-SGA, MNA, EFIP, GFI, Fried*s criteria, WHODAS 2.0, food diary. The burden of
these study measurements is minimal (about 70 minutes per study measurement at
the UMCG-rehabilitation center and 45 minutes in preparation). The risks of
these measurements are negligible. In the qualitative study, duration of the in
depth interviews is 60 min. at maximum.
Hanzeplein 1
Groningen 9700 RB
NL
Hanzeplein 1
Groningen 9700 RB
NL
Listed location countries
Age
Inclusion criteria
Aged 40 years or older
Able to understand and speak the Dutch language
Diagnosed with COPD by a pulmonary physician
Exclusion criteria
Wheel chair dependency
Any contra-indication for physical exercise
Severe cognitive disabilities
Skin allergy or highly sensitive skin
Palliative treatment
Pacemaker
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 |
---|---|
CCMO | NL49996.042.14 |