Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04993599
Other study ID # 2021-05-085-006
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2, 2021
Est. completion date January 31, 2022

Study information

Verified date July 2021
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is conducted for a mixed methods study. Subjects are 20 child patients and 20 their carers. First, Participants use and interact with a social robot. The robot is controlled by researcher with the wizard of oz. method. The interaction is video-recorded for the later analysis of the child's engagement through amount of his vocalization and sentences. After using social robot, a survey and an in-depth interview will be done. This study investigates the usability, satisfaction, emotion, and other dimensions of social robots of pediatric patients and carers and evaluate the degree of interaction with them with the recording data, survey and in-depth interview. This study is a basis for using social robots to pediatric patients in the hospital environments.


Description:

This study is conducted for a mixed methods study. Subjects are 20 child patients and 20 their carers. First, Participants use and interact with a social robot. The robot is controlled by researcher with the wizard of oz. method. And another researcher observes the participants-robot interaction. The interaction is video-recorded for the later analysis of the child's engagement through amount of his vocalization and sentences. After using social robot, a survey and an in-depth interview will be done. This study investigates the usability, satisfaction, emotion, and other dimensions of social robots of pediatric patients and carers and evaluate the degree of interaction with them with the recording data, survey and in-depth interview. This study is a basis for using social robots to pediatric patients in the hospital environments.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date January 31, 2022
Est. primary completion date January 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years and older
Eligibility <Pediatric patients> Inclusion Criteria: - Patients visiting Samsung Medical Center (Age 5~12) - A person who voluntarily agrees to participate in the study - Patients who are able to agree with a consent Exclusion Criteria: - Those who disagree with the study - Patients and carers who find it difficult to interact with the robot <Carers> Inclusion Criteria: - Caregivers of the patient participant - Adults over 19 years of age - A person who voluntarily agrees to participate in the study Exclusion Criteria: - Those who disagree with the study - Patients and carers who find it difficult to interact with the robot

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Social robot interaction
The participants interact with the social robot which is controlled by the researcher behind the scene (wizard of oz. method).

Locations

Country Name City State
Korea, Republic of Samsung Medical Centre Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration and time of robot communication with the participants Assessment of how long the duration and time of the communication between the participants ans robot is. Through study completion, an average of 1 year
Primary Number of conversations exchanged between the participant and the robot Assessment of the number of conversations exchanged between the participant and the robot Through study completion, an average of 1 year
Primary The amount of the incidence of participants' vocalization when interacting with the robot Assessment of the incidence of participants' vocalization when interacting with the robot. Through study completion, an average of 1 year
Secondary A qualitative study on user experience A qualitative study on user experience using a in-depth interview Through study completion, an average of 1 year
Secondary A quantitative study on the user experience A quantitative study on the user experience using User Experience Questionnaire. The items have the form of a semantic differential, i.e. each item is represented by two terms with opposite meanings. The items are scaled from -3 to +3. Thus, -3 represents the most negative answer, 0 a neutral answer, and +3 the most positive answer. Through study completion, an average of 1 year
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05975658 - WIReD: Wireless Interstage Remote Device Study
Completed NCT03921346 - Reducing Prehospital Medication Errors & Time to Drug Delivery by EMS During Simulated Pediatric CPR N/A
Completed NCT04301206 - Videos and Simple Text to Empower Parents to Handle Their Sick Children N/A
Not yet recruiting NCT04087070 - Blood Pressure Estimation Using Noninvasive Biosignals During Pediatric Anesthesia
Recruiting NCT06273228 - Parenting Young Children in Pediatrics N/A
Recruiting NCT05480930 - Improving Nighttime Access to Care and Treatment; Part 4-Haiti N/A
Not yet recruiting NCT05815563 - Validation of Peripheral Perfusion Index in Predicting Successful Supraclavicular Brachial Plexus Block in Pediatrics
Recruiting NCT02556541 - Ultrasound-guided Peripheral Vascular Access in Children N/A
Recruiting NCT02908113 - Visual Perception in Preterm Infants N/A
Not yet recruiting NCT01678066 - A Prospective Study to Bilaterally Compare a Non-Invasive Cardiac Output Monitor N/A
Completed NCT05537168 - Bayesian Networks in Pediatric Cardiac Surgery
Completed NCT01603628 - BOTOX® Treatment in Pediatric Lower Limb Spasticity Phase 3
Completed NCT01603615 - BOTOX® Open-Label Treatment in Pediatric Upper Limb Spasticity Phase 3
Completed NCT06098105 - Laparoscopic vs Ultrasound-Guided Transversus Abdominis Plane Block vs Laparoscopic Intraperitoneal Instillation of Local Anesthetic in Pediatrics N/A
Completed NCT01418846 - Determination of Voriconazole Levels in Saliva - Validation in Specific Subsets of Patients N/A
Completed NCT01460329 - Comparing Cardiac Output Measurements in Critically Ill Children Using USCOM and Transthoracic ECHO N/A
Withdrawn NCT00666393 - An Evaluation of Safety of the Fentanyl Transdermal System for Management of Acute Post-Operative Pain in Pediatric Patients Phase 3
Recruiting NCT03337581 - Pharmacodynamics and Pharmacokinetics of Dexmedetomidine in Pediatric Phase 4
Recruiting NCT05275881 - Impact of Virtual Reality in Pediatric Hematology and Oncology N/A
Recruiting NCT06146465 - Mobile Health Applications in Pediatric Patient Management: Clinicians' Perceptions, Expectations and Experiences