Use of the Mask and Current Pandemic (Mask)
Population Impact on the Continued Use of the Mask Due to the Avoidance of COVID-19
調査の概要
状態
条件
詳細な説明
Introduction
Due to the continued use of the mask in order to prevent the spread of COVID-19, an impact on people is observed in different areas. The objective of our study was to collect impact aspects related to the continued use of the mask that may affect the quality of life of the population.
Material and methods
Diseny. For this, an observational study has been carried out that includes an interview with aspects related to headaches, problems in the temporomandibular joint, headache impact and quality of life.
Participants. Subjects of all ages from 18 years old will be recruited who use a mask daily for the avoidance of COVID-19 and with the ability to answer the questions and complete the questionnaires. The study will be carried out at the Faculty of Physiotherapy of the University of Valencia. The participants will sign an informed consent guaranteeing the confidentiality of the data. The study is approved by the ethics committee of our institution.
Outcomes. The sociodemographic characteristics and the use of the mask will be collected. Subsequently, the evaluation instruments without the use of a mask and with the use of the same in: Headache and the impact on headaches, pain related to temporomandibular joint and quality of life.
All data will be coded in a database and analyzed later.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
-
-
Valencia、スペイン、46010
- Gemma Victoria Espí-López
-
-
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
説明
Inclusion Criteria:
- from 18 years old will be recruited who use a mask daily for the avoidance of COVID-19.
- that they use the face mask at least 2 hours a day
- with the ability to answer the questions and complete the questionnaires.
Exclusion Criteria:
- I do not use the mask
- institutionalized subjects
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
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 |
|---|---|---|
|
Headache
時間枠：1 day
|
An ad hoc questionnaire will be carried out that includes a question about the existence of headache before and after the use of the mask with a dichotomous response (Yes, No) and another about the frequency of headache with the options of daily, weekly or monthly.
|
1 day
|
|
Pain Temporomandibular Joint
時間枠：1 day
|
The ad hoc questionnaire will include two questions about the existence of joint discomfort in the TMJ before and after the use of the mask with a dichotomous response (Yes, No) and pain when chewing evaluated using the Visual Analog Scale (VAS).
|
1 day
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Headache Impact
時間枠：1 day
|
Headache Impact Test-6 (HIT-6).To measure the impact of headache.
The score is calculated as follows: never (6 points), few times (8 points), sometimes (10 points), very often (11 points) and always (13 points).
With a total of 49 or less points is considered "little or no impact", between 50-55 "some impact", between 56-59 "significant impact" and 60 or more "very severe impact".
|
1 day
|
|
Influence on quality of life
時間枠：1 day
|
Will be measured by Cantril Ladder of Life Scale (LADER).
The Cantril Staircase (Cantril 1965), measures satisfaction with life.
The subject is asked to imagine his life in the best possible way and to describe his hopes and wishes.
You are then asked to imagine your future in the worst possible light, your fears and concerns associated with this outcome.
Subsequently, the respondent is presented with an image consisting of a ladder numbered from zero to ten, where the top of the ladder represents the best possible life for the subject = 10 and the bottom of the ladder represents the worst possible life = 0.
|
1 day
|
協力者と研究者
スポンサー
捜査官
- 主任研究者：Gemma V Espí-López、fisiotherapy
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
キーワード
その他の研究ID番号
- ID0031
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
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。