Using Social Robots in Children With Rare Diseases and Their Parents: A Feasibility Study
Using Social Robots to Improve the Relationship and Alleviate Anxiety and Stress in Children With Rare Diseases and Their Parents: A Feasibility Study
National Yang Ming Chiao Tung University
21 participants
Jul 12, 2024
INTERVENTIONAL
Conditions
Summary
The goals of this clinical trial are to (a) evaluate the feasibility and acceptability of a social robot intervention for providing family-based care for rare diseases families and (b) explore the effectiveness of the social robot intervention in improving the parent-child relationships and alleviating stress and anxiety for rare diseases patients and their parents. The main questions are: * Is the social robot intervention suitable for and acceptable to rare disease patients and parents? * Does the social robot intervention improve the parent-child relationship of rare disease patients and their parents? * Does the social robot intervention alleviate the stress and anxiety of rare disease patients and their parents? Patients and their parents will interact with the social robot PARO separately and together in each 30-minute course every two weeks for four courses.
Eligibility
Inclusion Criteria6
- \[Patients\]
- Aged 8 to 19 years.
- Diagnosed with a rare disease.
- Be Able to communicate in Chinese. \[Parents\]
- A father or a mother of a child with a rare disease.
- Be Able to communicate in Chinese.
Exclusion Criteria10
- \[Patients\]
- Have a pacemaker.
- Have open wounds.
- Being infected with infectious diseases.
- Be unable to participate in social activities due to severe psychological disorder or cognitive dysfunction.
- \[Parents\]
- Have a pacemaker.
- Have open wounds.
- Being infected with infectious diseases.
- Be unable to participate in social activities due to severe psychological disorder or cognitive dysfunction.
Interventions
In the first and second courses, the patients and their parents freely interact with the social robot PARO for 30 minutes. In the third course, patients and their parents interact with PARO for 30 minutes using a worksheet that includes naming and recording characteristics of PARO. In the last course, patients and their parents interact with PARO for 30 minutes using a worksheet that freely recorded their observations about PARO and say goodbye to it.
Locations(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06466109