The objective of this research is reviewing the effectiveness of a methodology which aimes at giving content to demand-oriented care for people with dementia and caregivers and at being a useful tool for professional carers to provide demand-…
ID
Source
Brief title
Condition
- Dementia and amnestic conditions
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
People with dementia:
1. experienced degree of demand-oriented care
2. experienced quality of life
3. experienced quality of care
Caregivers:
1. experienced degree of demand-oriented care
2. experienced quality of life
3. experienced quality of care
4. the quantity met needs
5. the quantity unmet needs
6. experienced burden
7. feeling of competence
Care providers:
1. experienced competenties to be able to offer demand-oriented care
Secondary outcome
People with dementia:
4. the quantity met needs
5. the quantity unmet needs
Caregivers:
4. the quantity met needs
5. the quantity unmet needs
6. experienced burden
7. feeling of competence
Background summary
By the government policy, new legislation, and the rise of customer
organisations within the health care in the Netherlands, the last years the
emphasis has come to lie more and more on the active role of the customer in
the care attribution. Instead of offering 'supply-oriented care', institutions
try to offer 'demand-oriented' and sometimes 'demand-driven' health care. The
client perspective becomes normative for the aid offer and the organisation of
the health care. Among other things, care programmes are designed to realize
the 'demand-oriented' health care (Van Baalen, 2002).
In the region s-Hertogenbosch several care providers (nursing homes, home care
institution, general hospital and GGz) have taken the initiative to develop a
regional care programme for people with dementia. In a regional care programme
stands the whole care offer of the region for a specific target group in an
univocal manner defined. The basis for a care programme form the wishes and
needs of this specific target group. For this reason it is important to
inventory what the wishes and expectations are with respect to (quality of)
care of people with dementia and caregivers. This inventory forms the basis of
a PhD project. In this protocol the second phase of this project is described.
The first phase of the project has been performed in 2005-2006 and
implementation of it was approved by the Medical Ethical Testcommission for
institutions in the mental health care (METiGG, protocol 5,120) the results of
the first phase of the research (in which the term ' quality of care' from the
perspective of people with dementia at an early stage at issue was) has been
described in a separate report (Van Baalen, 2007).
At this second stage of the project the central objectives beside 'quality of
care' are 'needs' and 'quality of life'. In a concept model 'demand-oriented
care' these objectives are connected with each other. The idea has arisen that
a methodology which explores in a structured manner the needs of people with
dementia at an early stage and caregivers and the important aspects around
quality of care from the customer perspective can make a contribution to
forming demand-oriented care. Using this methodology ('Client Centred
Care-Dementia'- work name 'CCC-DEM') the care provider can clarify the care
needs of the customer and his caregiver in a systematic manner and it can be
useful in providing the care that qualitatively connects with what the customer
finds important.
Study objective
The objective of this research is reviewing the effectiveness of a methodology
which aimes at giving content to demand-oriented care for people with dementia
and caregivers and at being a useful tool for professional carers to provide
demand-oriented care.
Study design
This research has a quasi-experimental design. It does not meet all the
requirements of experimental research because complete blindness of the
intervention (use methodology) is not possible. The intervention is
single-blind applied (only the one who applies the intervention applies knows
this, the test person not). There will be an experimental and a control group
which will be composed by means of randomisation. One pretest and two posttest
measures will be done.
The design shows schematically as follows:
Time t 0 t1 t 2
R Group I O X C M O experimental group
R Group II O Xa M O control group
O *observation*: data are collected
X experimental intervention (use methodology)
Xa regular care
t 0,1,2 time 0 (pretest), time 1 (6 weeks after t0) and time 2 (3 months after
t 0)
C measurement of compliance
M care that results from the outcome of the methodology or regular care
R randomisation, by randomisation respondents are assigned to the experimental
or control group
Intervention
In the experimental group case managers the use a methodology with which the
needs of people with dementia and their caregivers can be clarified in a
systematic manner and it can be useful in providing the care that qualitatively
fits with what these people find important.
The control group receives regular care.
Study burden and risks
People with dementia at an early stage are asked to answer questions concerning
their perspective on the experienced quality of life, on the degree of
demand-oriented care, (un)met needs and the experienced quality of care. These
questions are conducted at 3 different times with people what will confiscate
in sum approximately 2.5 hour time (2x 1 hours and 1x 1/2 hours). The research
doesn't withhold any risks.
Postbus 70058
5201 DZ 's-Hertogenbosch
NL
Postbus 70058
5201 DZ 's-Hertogenbosch
NL
Listed location countries
Age
Inclusion criteria
People with dementia:
- diagnosis 'dementia' (GDS nivo 3-5; MMSE over 12 and under 24)
- client is capable to provide informed informed consent according to the casemanager involved
- client speaks Dutch language
- client is capable to concentrate in a conversation up to one hour
- client's ability to understand, hear and see is sufficient enough for the conversation according to the professional caregiver
- client has a central caregiver who wants to join the research project;Caregivers:
- caregiver provides care for a person with dementia who has agreed to take part in the research project
- caregiver is capable to provide informed consent
- caregiver speaks Dutch language
- caregiver is capable to fill in some questionnaires (duration about 1/2 uur)
Exclusion criteria
- diagnosis Mild Cognitive Impairment (MCI)
- suffering from severe behavioural problems
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 | NL24662.097.08 |