NCT06924801

Brief Summary

Emerging technologies that utilize motion capture integrated with engaging software offer new methods for increasing engagement and movement in patients admitted to the hospital. Hospitalized patients are often limited to sedentary activities, spending the majority of their time in bed, which can contribute to deconditioning and functional mobility deficits. This study seeks to explore the feasibility of a tool designed to promote movement through engaging gameplay that is acceptable to both clinicians and families.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
5mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress63%
Oct 2025Sep 2026

First Submitted

Initial submission to the registry

April 4, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 11, 2025

Completed
6 months until next milestone

Study Start

First participant enrolled

October 15, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Last Updated

December 18, 2025

Status Verified

December 1, 2025

Enrollment Period

12 months

First QC Date

April 4, 2025

Last Update Submit

December 11, 2025

Conditions

Keywords

motion capture technologyTotal translational movement

Outcome Measures

Primary Outcomes (1)

  • Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS)

    10-item questionnaire with a scale from 1- 5, 1 being strongly disagree to 5 being strongly agree on a five-point Likert scale to measure usability.

    Post-simulation (5 minutes)]

Secondary Outcomes (7)

  • Acceptability of Intervention Measure (AIM) survey

    immediately after the intervention

  • Intervention Appropriateness Measure (IAM) survey

    immediately after the intervention

  • Feasibility of Intervention Measure (FIM) survey

    immediately after the intervention

  • ISO 9241-400

    immediately after intervention

  • Setup time required for system use

    Before intervention

  • +2 more secondary outcomes

Study Arms (1)

Pediatric patient

EXPERIMENTAL

Pediatric patient will engage with engagement-focused software platform (Snipperfingers) and movement will be analysed by the real-time motion capture system (the OptiTrack system).

Behavioral: Snipperfingers

Interventions

SnipperfingersBEHAVIORAL

Snipperfinger is a self developed engagement focused software platform designed to encourage participation in pediatric physical therapy.

Pediatric patient

Eligibility Criteria

Age6 Years - 17 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Pediatric patients aged 6-17 years.
  • Receiving physical therapy at Stanford Children's Hospital.
  • Medically cleared for standing and upper-body movement.
  • Ability to follow simple instructions and engage in standing gameplay

You may not qualify if:

  • Orthopedic or medical conditions contraindicating physical activity.
  • Legal guardian not present to obtain consent
  • Child with a significant neurological condition or major developmental disability
  • Child with active infection of the face or hand
  • A history of severe motion sickness A history of seizures caused by flashing light Major surgery within the last 48 hours

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Lucile Packard Children's Hospital Stanford

Palo Alto, California, 94304, United States

RECRUITING

Central Study Contacts

Thomas Caruso, MD, PhD

CONTACT

Man Yee Suen, MMedSc

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Professor

Study Record Dates

First Submitted

April 4, 2025

First Posted

April 11, 2025

Study Start

October 15, 2025

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

September 30, 2026

Last Updated

December 18, 2025

Record last verified: 2025-12

Locations