Integration of Real-Time Motion Tracking and Pediatric Rehabilitation

Not Applicable

Not yet recruiting

• Conditions: Rehabilitation

• Registration Number: NCT06924801
• Lead Sponsor: Stanford University

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-04-04
• Study First Submitted QC: 2025-04-04
• Study First Posted: 2025-04-11
• Status Verified: 2025-05
• Last Update Submitted: 2025-05-22
• Last Update Posted: 2025-05-29
• Study Start: 2025-06-15
• Primary Completion: 2026-05-14
• Study Completion: 2026-05-14

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• 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

Exclusion Criteria

• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS)	Post-simulation (5 minutes)]	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.

Secondary Outcome Measures

Name	Time	Method
Acceptability of Intervention Measure (AIM) survey	immediately after the intervention	This questionnaire consists of 4 items. Measures are to be graded using a 1-5 scale, from 1=completely disagree, to 5= completely agree
Intervention Appropriateness Measure (IAM) survey	immediately after the intervention	This questionnaire consists of 4 items. Measures are to be graded using a 1-5 scale, from 1=completely disagree, to 5= completely agree
Feasibility of Intervention Measure (FIM) survey	immediately after the intervention	This questionnaire consists of 4 items. Measures are to be graded using a 1-5 scale, from 1=completely disagree, to 5= completely agree
ISO 9241-400	immediately after intervention	6-item ergonomic questionnaire with a scale from 1- 5, 1 being strongly disagree to 5 being strongly agree on a five-point Likert scale.
Setup time required for system use	Before intervention	Time required to set up the system, defined as the duration from participant arrival in the gym to the start of the physical activity.
Duration of gameplay-driven physical activity	immediately at the start of intervention, immediately after intervention	Time from first recorded movement in response to gameplay to last movement as recorded by OptiTrack motion capture or clinician observation
Evaluation parent's perception of patient's engagement.	immediately after intervention	Parent acceptance of the system will be evaluated by self developed questionnaire. The questionnaire contains 10 items with scale from 1-5, 1 being strongly disagree to 5 being strongly agree on a five-point Likert scale.

Trial Locations

Locations (1)

Lucile Packard Children's Hospital Stanford; 🇺🇸 Palo Alto, California, United States