3D Telemedicine: A Clinician Feedback Study
3D Telemedicine: Communication During Covid 19. A Clinician Feedback Study
調査の概要
詳細な説明
Aims The aim of this study is to assess 3D telemedicine and 2D telemedicine from the clinician's perspective, to optimise the system prior to clinical trials with patients. This will provide baseline validated outcome data on areas such as usability, presence (the realism or immersion of a system), mental effort and task load. "Keep, Lose and Change" prompts will be used to aid improvements in the 3D Telemedicine system prior to clinical trials.
Participants This will be a clinician feedback based study on 2D telemedicine and 3D telemedicine. Clinicians will include nurses, doctors and physiotherapists from Canniesburn Plastic Surgery Unit, Glasgow, UK.
Consent Clinicians will consent in writing to participate
Method Clinicians will use both 3D and 2D Telemedicine systems to examine a member of the research team who will act as a "patient". There will be a single clinician (consultant, nurse specialist or physiotherapist) examining the patient during the clinic.They will use each system for 10 minutes each. No randomisation will take place. This will be followed by a questionnaire which will be filled in once per patient by the clinician in the clinic.
Outcome measures No primary or secondary measures are specified as this is an observational feedback study, not an interventional clinical trial.
Satisfaction - Visual Analogue Scale 0-100 Mental Effort Rating Scale - single instrument Likert scale (Paas 1996) System Usability Scale - 10 item industry standard technology scale Presence Questionnaire - 29 item scale - assessment of presence in the system/virtual environment (PQ, Witmer 2005).
Semi Structured exit interview - will discuss with participant their views on the telemedicine system, using "Keep, Lose and Change" prompts to aid system improvements.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
-
Scotland
-
Glasgow、Scotland、イギリス、G4 0SF
- Canniesburn Regional Plastic Surgery and Burns Unit
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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
サンプリング方法
調査対象母集団
The study population will consist of a mix of clinicians from Canniesburn Plastic Surgery Unit including:
- doctors
- nurses
- physiotherapists These clinicians will be at varying levels of seniority, age and will be gender balanced, to provide generalisability of the results
説明
Inclusion Criteria:
- clinicians in Canniesburn Plastic Surgery Unit
- doctors
- nurses
- physiotherapists
Exclusion Criteria:
- visual problems whereby participant is legally blind
- cannot consent
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
コホートと介入
グループ/コホート |
介入・治療 |
---|---|
3D Telemedicine
Clinical consultation conducted with 3D Telemedicine
|
3D Telemedicine system
|
2D Telemedicine
Clinical consultation conducted with 2D Telemedicine
|
2D Telemedicine system
|
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 |
---|---|---|
Clinical Satisfaction
時間枠:1 day (Single time point post study)
|
Satisfaction measured on a Visual Analogue Scale between 0-100.
Higher is better (Voutilainen et al. 2016).
|
1 day (Single time point post study)
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
---|---|---|
System Usability Scale
時間枠:1 day (Single time point post study)
|
10 item industry standard technology scale, scores converted to a 0-100 scale.
Higher is better
|
1 day (Single time point post study)
|
Presence Questionnaire
時間枠:1 day (Single time point post study)
|
29 item scale - assessment of presence in the system/virtual environment.
Score 0-203, Higher is better (PQ, Witmer 2005).
|
1 day (Single time point post study)
|
Mental Effort Rating Scale
時間枠:1 day (Single time point post study)
|
Single instrument Likert scale rated 1-9.
Lower is better (Paas 1996)
|
1 day (Single time point post study)
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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
その他の研究ID番号
- GN20HS181
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
3D Telemedicineの臨床試験
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Washington University School of MedicineAllergan完了
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Guy's and St Thomas' NHS Foundation TrustKing's College Londonまだ募集していません
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First Affiliated Hospital Xi'an Jiaotong Universityわからない
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Olympus Corporation of the AmericasInternational Urogynecology Associates完了
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Cairo Universityわからない