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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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Children's Hosptial and Medical Center
Coordinator of this site? Confirm its status
OmahaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.