Integration of Real-Time Motion Tracking and Pediatric Rehabilitation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Snipperfingers.
- Who it may be relevant to
- Registry conditions: Rehabilitation. Basic parameters: 6 years — 17 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluating the Feasibility, Usability, and Integration of the OptiTrack Motion Capture System in Inpatient Physical Therapy
Overview
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.
Interventions
- Behavioral Snipperfingers
Snipperfinger is a self developed engagement focused software platform designed to encourage participation in pediatric physical therapy.
Primary outcome measures
- Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS) [Time frame: Post-simulation (5 minutes)]]
Secondary outcome measures (7)
- Acceptability of Intervention Measure (AIM) survey [Time frame: immediately after the intervention]
- Intervention Appropriateness Measure (IAM) survey [Time frame: immediately after the intervention]
- Feasibility of Intervention Measure (FIM) survey [Time frame: immediately after the intervention]
- ISO 9241-400 [Time frame: immediately after intervention]
- Setup time required for system use [Time frame: Before intervention]
- Duration of gameplay-driven physical activity [Time frame: immediately at the start of intervention, immediately after intervention]
- Evaluation parent's perception of patient's engagement. [Time frame: immediately after intervention]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- Lucile Packard Children's Hospital Stanford — Palo Alto
Identifiers
NCT: NCT06924801 · 80334