Big Data Analysis of OSA Patients on Positive Airway Pressure (PAP) Treatment: Real-life Monitoring (TeleVAL)
Big Data Analysis of OSA Patients on Positive Airway Pressure (PAP) Treatment: Real-life Monitoring: TeleVAL Study
The present study aims to determine to what extent remote monitoring of PAP related to patients' clinical parameters is able to provide relevant data on predictors of compliance, subgroups of patients who may benefit from this technological tool, variations in AHI over time, occurrence of central events at the start of therapy and, in short, to shed new light on this disease and its treatment, all within the application of continuous positive pressure therapy in the real world.
Among the intended objectives is the identification of phenotypes involved in the use and efficacy of PAP therapy: development of a predictive model, as well as the evaluation of the impact of long-term telemonitoring of patients with Obstructive Sleep Apnea (OSA).
The study initially arose from the need to diagnose, treat and follow up patients with suspected OSA in compliance with the social distancing rules imposed by the COVID-19 pandemic.
It is an ambispective cohort study, with retrospective data collection from the start date of the pandemic (March 2020) to December 2021, and prospective data collection from the approval of the protocol to December 2022.
調査の概要
研究の種類
入学 (予想される)
連絡先と場所
研究連絡先
- 名前：monica Gonzalez
- 電話番号：+34942203389
- メール：monica.gonzalezm@scsalud.es
研究連絡先のバックアップ
- 名前：Lucía Lavin
- 電話番号：+34942203389
- メール：eclinicos5@idival.org
研究場所
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Cantabria
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Santander、Cantabria、スペイン、39008
- 募集
- Hospital Universitario Marques de Valdecilla
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コンタクト：
- Monica Gonzalez
- メール：monica.gonzalezm@scsalud.es
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参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
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
説明
Inclusion Criteria:
- All patients diagnosed with OSA since March 2020 with indication for treatment with PAP have been telemonitored on an ongoing basis since initiation of therapy continuing to be telemonitored at the current time.
Exclusion Criteria:
- Undiagnosed OSA patients
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 |
|---|---|
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Registry of patients
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All patients diagnosed with OSA since March 2020 with an indication for treatment with PAP have been telemonitored permanently since the start of therapy and continue to be telemonitored at the present time.
Data are sent remotely daily to the telemonitoring platform.
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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 |
|---|---|---|
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Characterize the phenotypes involved
時間枠：pandemic start date March 2020 until December 2022.
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Determine the emergent CSA appearance in relation to PAP treatment.
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pandemic start date March 2020 until December 2022.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Establish the percentage of patients who at the first connection to the TM achieved the optimal therapeutic pressure
時間枠：pandemic start date March 2020 until December 2022.
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According to Built in software (BIS) of the equipment
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pandemic start date March 2020 until December 2022.
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Establish the Profile of patients who at the first connection to the TM achieved the optimal therapeutic pressure
時間枠：pandemic start date March 2020 until December 2022.
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According to Built in software (BIS) of the equipment
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pandemic start date March 2020 until December 2022.
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Variations in AHI during the first year of follow-up and their relationship with patient characteristics.
時間枠：pandemic start date March 2020 until December 2022.
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pandemic start date March 2020 until December 2022.
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Time to achieve the optimal therapeutic pressure described after the first connection
時間枠：pandemic start date March 2020 until December 2022.
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Number of modifications required and their relationship with patient subgroups.
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pandemic start date March 2020 until December 2022.
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Evaluation of the impact of long-term telemonitoring of patients with OSA
時間枠：pandemic start date March 2020 until December 2022.
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Number of acesses and interventions made to the telemonitoring platform/year and time invested
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pandemic start date March 2020 until December 2022.
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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 (予想される)
研究の完了 (予想される)
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
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。