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Grip op probleemgedrag bij jonge mensen met een dementie: de Beyond-II studie

Grip on neuropsychiatric symptoms in young-onset dementia: the Beyond-II study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21079
Enrollment
200
Registered
2015-02-20
Start date
2015-09-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Neuropsychiatric symptoms in young-onset dementia

Interventions

In this intervention study, the adapted Grip on challenging behavior care program will be implemented at ten YOD SCU's. A stepped wedge design will be used in which eventually all special care units w

Sponsors

Radboud University Medical Center (RadboudUMC), Nijmegen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Residents of young-onset dementia special care units (YOD SCU’s) of the Dutch young-onset dementia Knowledge Centre (DKC) with an established dementia diagnosis according to regular criteria will be included in the study. Residents with a symptom onset before the age of 65 are included in the study, thus residents can be over the age of 65. Prerequisite for inclusion will be informed consent of the resident and/or his legal representative. Deceased and discharged residents are replaced by newly admitted residents.

Exclusion criteria

Exclusion criteria: Residents with symptom onset after the age of 65 or residents with a history of other neurological disorders (i.e. head injury, stroke, Korsakoff’s syndrome, multiple sclerosis) will be excluded.

Design outcomes

Primary

MeasureTime frame
Agitation and Aggression as measured with the Dutch version of the Cohen-Mansfield Agitation Inventory (CMAI-D) Neuropsychiatric Symptoms measured with the Dutch version of the Neuropsychiatric Inventory-NH version (NPI-NH)

Secondary

MeasureTime frame
Resident related outcomes: Quality of life of the resident measured with the Quality of Life in Dementia (Qualidem) Psychotropic drug use (PDU) will be derived from medical files and classified using the Anatomical Therapeutical Chemical Classification. Nursing staff related outcomes: Workload measured with the Utrecht Burnout Scale-C (UBOS-C) Job satisfaction and work/time pressure is assessed with two subscales of the Leiden Quality of Work Questionnaire Absence rate will be retrieved from periodical registrations done by the personnel departments of participating nursing homes. Other outcomes: Sociodemographic variables Length of stay in the nursing home Dementia Type will be classified with the DSM-IV-TR Dementia severity with the Global Detoriation Scale (GDS) Environmental factors of the dementia care unit will be assessed with the Therapeutic Environment Screening Survey for nursing homes (TESS-NH) Nursing staff attitude will be measured with the Approaches to Dementia Questionnaire (ADQ)

Contacts

Public ContactChristian Bakker
Christian.Bakker@radboudumc.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)