リアルタイムモーショントラッキングと小児リハビリテーションの統合：前向きコホート研究 (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.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究場所
-
-
California
-
Palo Alto、California、アメリカ、94304
- Lucile Packard Children's Hospital Stanford
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：支持療法
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：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. |
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS)
時間枠：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. |
Post-simulation (5 minutes)]
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Acceptability of Intervention Measure (AIM) survey
時間枠：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
|
|
Intervention Appropriateness Measure (IAM) survey
時間枠：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
|
|
Feasibility of Intervention Measure (FIM) survey
時間枠：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
|
|
ISO 9241-400
時間枠：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. |
immediately after intervention
|
|
Setup time required for system use
時間枠：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. |
Before intervention
|
|
Duration of gameplay-driven physical activity
時間枠：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 |
immediately at the start of intervention, immediately after intervention
|
|
Evaluation parent's perception of patient's engagement.
時間枠：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. |
immediately after intervention
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- 80334
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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