실시간 모션 추적 및 소아 재활의 통합 : 전향 적 코호트 연구 (Snipperfinger)
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.
연구 개요
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 장소
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California
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Palo Alto, California, 미국, 94304
- Lucile Packard Children's Hospital Stanford
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 지지 요법
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Pediatric patient
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). |
Snipperfinger is a self developed engagement focused software platform designed to encourage participation in pediatric physical therapy. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS)
기간: Post-simulation (5 minutes)]
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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)]
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Acceptability of Intervention Measure (AIM) survey
기간: immediately after the intervention
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This questionnaire consists of 4 items. Measures are to be graded using a 1-5 scale, from 1=completely disagree, to 5= completely agree |
immediately after the intervention
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Intervention Appropriateness Measure (IAM) survey
기간: 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 |
immediately after the intervention
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Feasibility of Intervention Measure (FIM) survey
기간: 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 |
immediately after the intervention
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ISO 9241-400
기간: immediately after intervention
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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. |
immediately after intervention
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Setup time required for system use
기간: Before intervention
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Time required to set up the system, defined as the duration from participant arrival in the gym to the start of the physical activity. |
Before intervention
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Duration of gameplay-driven physical activity
기간: immediately at the start of intervention, immediately after intervention
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Time from first recorded movement in response to gameplay to last movement as recorded by OptiTrack motion capture or clinician observation |
immediately at the start of intervention, immediately after intervention
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Evaluation parent's perception of patient's engagement.
기간: immediately after intervention
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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. |
immediately after intervention
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .