A Preliminary Study on the Application of Family-type Robot (LOVOT) in Medical and Clinical Practice

A Preliminary Study on the Application of Family-type Robot (LOVOT) in Medical and Clinical Practice - A Preliminary Study on the Application of Family-type Robot (LOVOT) in Medical and Clinical Practice

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000046098

Enrollment

Registered

2021-11-17

Start date

2020-11-20

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Pediatric patients, rehabilitation patients, oncology-related patients(obstetrics and gynecology, breast surgery, medical oncology), nurses

Interventions

Rehabilitation patients will be monitored for a total of two weeks, one week each with and without LOVOT. All other patients and health care providers will be assessed for one week with LOVOT. Rehabi

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The patients were selected by the attending physician based on their disease and condition.

Exclusion criteria

Exclusion criteria: The patients who are unsuitable by attending physician in consideration of their disease and condition.

Design outcomes

Primary

Measure	Time frame
To evaluate the change in the state of mind before and after the introduction of LOVOT to patients and their parents or medical staff. To evaluate behavioral changes on the video for rehabilitation patients.	—

Countries

Japan

Contacts

Public ContactYasuyuki Kobayashi

St. Marianna University School of Medicine Medical Information and Communication Technology Research

yasukoba@marianna-u.ac.jp044-977-8111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026