NCT05275543Completed
Robot Rehab: AAI With Robot During Inpatient Pediatric Rehab
Robot Rehab: Animal Assisted Interactions With a Robotic Baby Harp Seal During Inpatient Pediatric Rehabilitation
Source: ClinicalTrials.gov · Last updated 28 Oct 2026
Brief summary (registry, in English)
The purpose of this study is to: Aim 1: Evaluate the feasibility \[consent and refusal rates, attrition rates, length, and number of completed therapy sessions\], and acceptability \[interviews with children and guardians, overall patient and guardian satisfaction\] during inpatient physical therapy (PT) and occupational therapy (OT) sessions. Hypothesis: Animal-assisted interaction (AAI) with Paro, a robotic baby harp seal, during pediatric inpatient PT/OT sessions will be feasible and acceptable. Aim 2: Assess preliminary efficacy of AAI during PT/OT sessions with Paro on behavior (anxiety and affect) and motivation to participate in rehabilitation in hospitalized children. Hypothesis: Children who use Paro will demonstrate less anxiety, more positive affect, and greater motivation to participate in therapy than those who do not use Paro. Aim 3: Test the stress, anxiety, and depression levels of parents/guardians of children who use Paro inpatient physical and occupational therapy sessions. Hypothesis: In addition, parents and guardians of children that use Paro will report less stress, anxiety, and depression compared to parents/guardians of children that do not use Paro.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 51 (actual)
- First submitted
- 25 Feb 2022
- Start date
- 1 Apr 2022
- Primary completion date
- 3 Jan 2025
- Lead sponsor
- University of Nebraska
- NCT number
- NCT05275543
What you commit to
- Study type: Interventional
- Participants enrolled: 51
- From 1 Apr 2022 to the primary completion date, 3 Jan 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Have a pacemaker
- have airborne, enteric, or enhanced contact precautions
- wounds without a covering dressing or a dressing that is visibly soiled
- known adverse psychological reactions to animals
- excessive secretions via nose or mouth
- report feeling nauseated
- shows signs of acute agitation (yelling, screaming, moaning, or is otherwise inconsolable).
Who the study is looking for
- Age 5-18
- admitted to any of the five inpatient units at Children's Hospital and Medical Center, Omaha, NE
- have an available parent or guardian
- have an active consult request for PT or OT
- awake, alert, able to follow commands
- not delirious
- able to understand English
- free from significant vision or hearing deficits
- able to verbalize.
Age in the registry: 5 years to 18 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Children's Hosptial and Medical Center Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.