Effects and Costs of a Day Care Centre Program Designed for People With Dementia
- Conditions
- Dementia
- Interventions
- Behavioral: Day care for patients with dementia
- Registration Number
- NCT01943071
- Lead Sponsor
- Norwegian Centre for Ageing and Health
- Brief Summary
Attending day care centres with programs specifically designed for patients with dementia is believed to postpone admittance to nursing home as well as increase quality of life and well-being for both patients and their family caregivers. We aim to investigate to what degree attendance in day care centres with programs for people with dementia is effective for patient and their caregivers whilst also cost efficient for society. The study consists of a quasi-experimental trial with comparison group. 400 patients with dementia, along with a family caregiver, will be included in the trial. Effects will be measured at baseline, after one and two years. Data collection will be made at three levels; at patient level with measures of cognition, depression, quality of life, functioning in activities in daily living, neuropsychiatric symptoms and death; at caregiver level with measures of depression, level of burden and quality of life; and at societal level with measures of nursing home admittance, hospital stays and use of other health resources. Additionally,a qualitative interview study will include 20 dyads from the main trial. The main focus will be on how attending day care centre programs for patients with dementia affect the lives of both patients and caregivers. Five of these dyads will be followed closely throughout the participation period to be used as case examples.
- Detailed Description
A quasi experimental trial with a comparison group will be performed to evaluate the effect of the day care centre programs by comparing results from municipalities with (intervention group) and without (comparison group) a day care centre program designed for people with dementia using standardized assessment tools. Furthermore, a survey will be used to explore the communication and co-operation between the professional staff at the day care centre, the patients and the family carers by administering questionnaires to all three parties. Only patients with mild degree of dementia will be asked to participate in the questionnaire. Finally, qualitative interviews will be made with 20 dyads of patients and family carers to collect their in depth experience with the day care centre program. Five of these patients and their family carers will be followed closely as case examples for two years.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 261
- Age of 65 years or more and living at home
- Patients in the day care centre group must have attended the centre for at least four weeks and have been there no longer than nine months
- Dementia of either Alzheimer's type, vascular dementia, dementia with Lewy bodies/Parkinson's disease or a mixture of these types of dementias
- Capacity to give informed consent as judged by the professional caregivers
- A Mini Mental Status Examination (MMSE) score of ≥15
- Having a family carer willing to participate, who see the patients personally at least once a week
- Attending the day care centre program at least twice a week
- Having applied for nursing home placement
- Suffering from a serious co-morbid physical disorder with life expectancy less than six months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Day care for patients with dementia Day care for patients with dementia Day care for patients with dementia
- Primary Outcome Measures
Name Time Method Admittance to nursing home care 24 months The number of patients admitted to nursing home care during a period of 24 months will be the primary outcome for the effect and the cost-consequence analysis
- Secondary Outcome Measures
Name Time Method Change in family carers depressive symptoms 12 and 24 months The MADRS will be used to assess depressive symptoms in family carers
Differences in the use of health resources between the intervention group and the control group 12 and 24 months The use of health resources will be measured using the resource Utilization in Dementia scale (RUD)
Differences in quality adjusted life years between the intervention group and the control group 12 and 24 months A generic instrument, the EuroQol (EQ-5D) will be used to measure quality adjusted life years
Change in depressive symptoms in patients 12 and 24 months The change in depressive symptoms will be assessed by Montgomery Asberg Depression Rating Scale (MADRS)by interviews with both patient and family carer and the Cornell Scale for Depression in Dementia (CSDD) by interviews with family carers and a professional caregiver
Change in patient's cognition 12 and 24 months Patient's cognition will be assessed using the Mini Mental State Examination (MMSE) the Clock Drawing Test (CDT), the Trail Making Test A (TMT-A)and the 10 word test of the Consortium to Establish a Registry in Alzheimer's Disease (CERAD)
Change in quality of life for family carers 12 and 24 months QoL-AD will be used to assess quality of life in family carers
Change in neuropsychiatric symptoms in patients 12 and 24 months The change in Neuropsychiatric symptoms will be assessed using Neuropsychiatric Inventory Questionnaire (NPI-Q)
Change in the patient's functioning of daily living 12 and 24 months The Physical self-Maintenance Scale and Instrumental Activities of Daily Living Scale will be used to assess change in the patient's function of daily living
Patients death 24 months Number of patients that have died during 24 months will be registered
Change in level of burden in family carers 12 and 24 months Level of burden for family carers will be assessed by using the Relative's Stress Scale (RSS)
Change in Quality of life for patients 12 and 24 months The quality of life for patients as measured by Quality of Life - Alzheimer's Disease (QoL-AD)
Trial Locations
- Locations (1)
Norwegian centre of Ageing and Health
🇳🇴Tønsberg, Norway