Video Extradition of Continuous Positive Airway Pressure - Influence on Compliance
調査の概要
詳細な説明
Due to increasing age, BMI and increased focus on obstructive sleep apnea syndrome (OSAS) in the background population, an increasing number of obstructive sleep apnea (OSA) patients are expected to occur in the coming years. This is accompanied by a need for multiple deliveries of CPAP equipment, which is the recommended treatment. A large proportion of patients are young and healthy with their OSA. There is an increased focus on telemedicine and much of the control of patients has been transferred to ambuflex, where treatment effect or treatment problems can be more easily detected. Socioeconomically, the deliveries, together with the medical examination, are resource-intensive and they also take up a lot of the patient's time and often at distant times. The quality of disclosure and information varies greatly in both time and amount of information. The large amount of information can be difficult to remember for patients and relatives. Most investigations require more visits to the hospital and therefore potentially provide several days away from work.
A similar trial has never been made, but randomized studies have been made in the past where the delivery of CPAP or low compliance patients has been supported by a motivational video or teaching with good effect. Studies have also been conducted that have attempted to identify CPAP dropout and compliance based on gender, age, educational level and personality, with unemployment being the only contributing prognostic factor in the negative direction. It is well-studied that if patients suffer from insomnia, the onset of CPAP can be difficult and this patient group should be monitored more closely and possibly. have additional help for startup.
The video in this study provides a brief review of illness and treatment, instruction on assembling and adapting equipment, and answers to the most frequently asked questions. Both groups are given the same telephone numbers as usual, for questions and here it will be included in the study if there is a difference in the amount of contacts to the ambulatory. The video has been tested in the relevant setting before starting the project. M Gaglianos made in 1988 is a literature review showing that video teaching is good and more effective than traditional teaching methods, with effects on short-term but not long-term memory.
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
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:
- candidate to CPAP
- over age of 18
Exclusion Criteria:
- Language issues
- sight or hearing handicap
- kognitive issues
- if drivers license is confiscated
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:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- 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 |
|---|---|
|
介入なし:nurse instruction of CPAP
Normal extradition.
45 minutes face to face with a nurse.
|
|
|
実験的:Video extradition
Access to 7 min video - explaining how to start CPAP and how to adjust the mask.
|
No drugs used.
The only difference in the to arms is the way the extradition is.
|
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 |
|---|---|---|
|
compliance in percentage
時間枠:one month.
|
Compliance at one month follow up.
Minimum 0 % maximum 100 % compliance.
|
one month.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Depression
時間枠:one month.
|
Depression measured by major depression index (MDI) questionnaire.MDI total score < 20 being normal and not depressed.
MDI total score > 29 indicating severe depression.
|
one month.
|
|
Influencer
時間枠:one month.
|
Education level registered by ISCED 2011 levels of education.
Level 0-8.
8 being doctoral or equivalent.
0 being Early childhood Education (01 Early childhood educational development)
|
one month.
|
|
Insomnia
時間枠:One month .
|
Insomnia measured by insomnia severity index (questionnaire).
0-12 points.
0 being no problems facing a sleep.
12 having lots og trouble falling a sleep.
|
One month .
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Jesper Bille, MD、University Aarhus
研究記録日
主要日程の研究
研究開始 (予想される)
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
本研究に関する用語
その他の研究ID番号
- 15022020
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?
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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