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Evaluation of emotion-oriented care versus usual care for elderly persons with dementia in the nursing home

Integrated emotion-oriented care versus usual care for elderly persons with dementia in the nursing home: a clinical experimental study into the effects and costs

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15609358
Enrollment
271
Registered
2009-08-27
Start date
1996-04-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Dementia, psychogeriatrics Mental and Behavioural Disorders Unspecified dementia

Interventions

Intervention: Dutch Model Care plan and integrated emotion-oriented care, partly based on the validation approach, partly based on elements of other psychosocial care strategies/approaches in dementia
n = 32 caregivers per ward of 30 residents) and some of them also an advanced course (7 days
one out of 4 caregivers who passed the basic course). The pre-experimental period was 6 months, the intervention period (actual implementation of integrated emotion-oriented care) was 7 months. Pre-

Sponsors

The Dutch Health Care Insurance Board (CVZ) (Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients: 1.1. Persons older than 65 years of age, either sex 1.2. Probable diagnosis of dementia of the alzheimer-type (DAT), mixed diagnosis of DAT and vascular dementia, amnestic syndrome and dementia syndrome not otherwise specified 1.3. In need of assistance or care 1.4. Living in nursing homes for at least one month before the start of the baseline measurement 2. Professional caregivers in the experimental group: 2.1. Certified nursing assistants that followed the course Validation-worker 2.2. First responsible nurse assistants 3. Professional caregivers in the control group: 3.1. Nurse assistants that were matched with the experimental group on education, age and work experience 3.2. Did not participate in any course of Validation-worker 4. Relatives: frequence of visiting the resident with dementia at least ones a month

Exclusion criteria

Exclusion criteria: 1. Patients: refusal to participate in the study 2. People who did not fullfil the inclusion criteria 3. People with severe physical disabilities (such as total blindness or muteness), that made adequate data collection for the effect study impossible 4. Professional caregivers: 4.1. Did not fulfil the inclusion criteria 4.2. Were not prepared to participate in the study

Design outcomes

Primary

MeasureTime frame
1. Behaviour and mood problems as symptoms of difficulties with the cognitive, emotional and social adaptation to the consequences of the disease and nursing home admittance 2. Positive behaviour, affect and institutionalisation All measurements of this implementation effectiveness study took place at baseline and after 7 months.

Secondary

MeasureTime frame
General health of professional caregivers: 1. Stress experience 2. Stress reactions 3. Illness 4. Sense of competence All measurements of this implementation effectiveness study took place at baseline and after 7 months.

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026