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Animal-assisted or Robot-assisted Interventions in Health Promotion for Elderly With Dementia

Not Applicable
Completed
Conditions
Dementia
Registration Number
NCT01998490
Lead Sponsor
Norwegian University of Life Sciences
Brief Summary

The overall research aim of this study is to investigate changes in measures related to the risk of falls among elderly with dementia participating in animal-assisted or robot-assisted interventions. In addition the study will investigate how knowledge transfer occurs among involved health personnel, and how knowledge is refined and transformed as practical competence. The design will be a prospective and cluster randomized multicenter trial, but mixed-methods will be used to target different outcomes. The study population will be elderly (age above 65) at nursing homes diagnosed with dementia, or having a cognitive deficit. The intervention will consist of 30 minutes sessions with animal-assisted activity or robot-assisted activity two times a week for 12 weeks in groups of 4-6 participants. Control groups will receive treatment as usual. Research questions:

1. Is there an effect in use of ordinary and optional medication among elderly persons with dementia at nursing homes participating in animal-assisted or robot-assisted interventions compared to a control group?

2. Is there an effect on agitation, restlessness and depression among elderly persons with dementia at nursing homes participating in animal-assisted or robot-assisted interventions compared to a control group?

3. Is there an effect on social interaction, activeness and wellbeing among elderly persons with dementia at nursing homes participating in animal-assisted or robot-assisted interventions compared to a control group?

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
88
Inclusion Criteria
  • Diagnosis of dementia or having a cognitive deficit measured as a score less than 25 on Mini-Mental State Examination.
Exclusion Criteria
  • Fear of dogs
  • Dog allergy
  • Need of wheel chair

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in Norwegian version of The Brief Agitation Rating ScaleSecond last or last week before the intervention starts, after 4 and 8 weeks of the intervention, and first or second week after end of intervention. A follow-up measure 3 months after end of the intervention
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (15)

Pålsetunet bo- og servicesenter

🇳🇴

Fet, Norway

Solliheimen Sykehjem

🇳🇴

Fredrikstad, Norway

Solheimen senter

🇳🇴

Halden, Norway

Frida Sykehjem

🇳🇴

Larvik, Norway

Lørenskog Sykehjem, avd. Losbyveien

🇳🇴

Lørenskog, Norway

Løreskog sykhjem, avd Krydderhagen

🇳🇴

Lørenskog, Norway

Orkerød Sykehjem

🇳🇴

Moss, Norway

Ryggeheimen

🇳🇴

Moss, Norway

Gipø Sykehjem

🇳🇴

Nøtterøy, Norway

Greverud Sykehjem

🇳🇴

Oppegård, Norway

Scroll for more (5 remaining)
Pålsetunet bo- og servicesenter
🇳🇴Fet, Norway

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