MedPath

A study on the Effects of Socially Assistive Robots (SAR) in Intramural Elderly Health Care * A Quasi Experimental Trial.

Completed
Conditions
Alzheimer
dementia
10012272
Registration Number
NL-OMON37472
Lead Sponsor
Zuyd University of Applied Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

1. Dementia
2. Undesirable psychological / psychosocial unrest or mood
3. Experienced difficulties in provision of daily care

Exclusion Criteria

1. No written consent
2. Medical (somatic or psychiatric) objections against participation formulated by the Multidisciplinary team (MDO).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary objective of this study is to assess the effectiveness of Paro on<br /><br>individually (per subject) and short-term (during and after treatment) defined<br /><br>goals.<br /><br>The goals can be categorized into two main groups:<br /><br>1. For therapeutic purposes, involving psychological functioning, psychosocial<br /><br>well-being, social behavior and reactivation.<br /><br>2. To facilitate daily care activities.<br /><br><br /><br>During each of the 4 periods (A, B, A, B) the behavior of the participants is<br /><br>measured 5 times by a Goal Attainment Scale i.e. the IPPA-score (Individually<br /><br>Prioritized Problems Assessment).</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>1. Psychological and psychosocial functioning during treatment (facilitating<br /><br>daily care activities).<br /><br>The psychological and psychosocial functioning of the participant is measured<br /><br>based on a mood scale. The frequency of the measurements is equal to the<br /><br>measurements of the primary objective.<br /><br><br /><br>2. Experienced practical issues by care providers: semi structured<br /><br>questionnaires.<br /><br>During the interventions (i.e. periods A en B) a questionnaire will be<br /><br>conducted with the involved care providers, per participant, by the observer or<br /><br>the investigator(s), at the end of each period. Resulting in 4 questionnaires<br /><br>per participant</p><br>
© Copyright 2025. All Rights Reserved by MedPath