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Can the companion robot Paro improve quality of life in a residential care facility: A randomised controlled trial

Can the companion robot Paro improve quality of life in a residential care facility: A randomised controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000469819
Enrollment
40
Registered
2012-04-30
Start date
2012-04-16
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

To evaluate the benefits of the companion robot Paro for use at an residential care facility. By randomly assigning residents to a control group or an intervention group where participant use Paro over 12 weeks the benefits of the robot on well being can be assessed over this period. It is expected that the robot will improve quality of life, reduce depression and loneliness over this time in comparison to residents who have no contact with the robot

Interventions

Paro is a robotic fluffy seal designed to act like an animal. Paro was designed to be used in a similar way to live animals during animal therapy in elder care facilities. The intervention group has two 1 hour group sessions run by a caregiver with Paro each week for 12 weeks where each resident has the chance to interact with Paro and discuss the robot with others in the group. Caregivers have also been trained to use Paro with those in the group outside of activity sessions if a resident is

Paro is a robotic fluffy seal designed to act like an animal. Paro was designed to be used in a similar way to live animals during animal therapy in elder care facilities. The intervention group has two 1 hour group sessions run by a caregiver with Paro each week for 12 weeks where each resident has the chance to interact with Paro and discuss the robot with others in the group. Caregivers have also been trained to use Paro with those in the group outside of activity sessions if a resident is upset

Sponsors

University of Auckland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No

Inclusion criteria

Residents living in the resthome or the hospital at Selwyn Heights Residential Care Facility in Auckland, New Zealand and identified by the management care staff as suitable participants

Exclusion criteria

None

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026