Digital Stimulation and Anxiety and Sleep Quality in Intensive Care Unit Patients
The Effect of Digital Visual and Auditory Stimulation on Anxiety and Sleep Quality in Patients Hospitalized in the Intensive Care Unit: A Randomized Controlled Trial
The aim of this study is to examine the effect of digital visual and auditory stimulation on anxiety and sleep quality in patients hospitalized in the intensive care unit (ICU).
The questions to be answered within the scope of the research are:
Does the application of digital visual and auditory stimulation to patients in intensive care units have a significant effect on anxiety levels? Does the application of digital visual and auditory stimulation to patients in intensive care units have a significant effect on sleep quality? Does the application of digital visual and auditory stimulation to patients in intensive care units have a combined effect on anxiety levels and sleep quality?
Participants will:
The patients will be divided into two groups: an intervention group and a control group. The intervention group will receive visual and auditory stimuli once a day, every morning for three days. Sleep quality and anxiety levels will be measured after the digital visual and auditory stimuli.
The control group will continue with routine intensive care unit follow-up treatments.
調査の概要
詳細な説明
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Esra Başer Akın
- 電話番号:+90 538 478 06 60
- メール:esra_baser568@hotmail.com
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- 18 years and above
- Conscious [Glasgow Coma Scale(GCS)] ≥ 14)
- Not connected to mechanical ventilation or receiving non-invasive support
- Hearing and visual functions are sufficient
- No communication problems
- Able to answer questions correctly
- Not under sedation
- Expected to stay in the ICU for at least 48 hours
Exclusion Criteria:
- Having a hearing or visual impairment
- Being under sedation
- Having impaired consciousness
- Refusing to participate in the study
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:ヘルスサービス研究
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Intervention Group: Digital Visual and Auditory Stimulation
Patients in the intervention group will receive visual and auditory stimuli once a day, every morning for three days.
Visually, they will be shown landscape images on a tablet.
Simultaneously, they will listen to classical music (60-80 bpm) through headphones.
As a pre-test, patients in the intervention group will complete a questionnaire, the Richards-Campbell Sleep Scale, and the Hospital Anxiety and Depression Scale.
These scales will also be administered as a post-test on the third day.
|
Visually, they will be shown landscape images on a tablet.
Simultaneously, they will listen to classical music (60-80 bpm) through headphones.
|
|
介入なし:Control Group: Usual Care
Patients in the control group will also be administered the Richards-Campbell Sleep Scale (RCSQ) and the Hospital Anxiety and Depression Scale (HADS) at the beginning of the data collection process, at the same time as the intervention group.
Patients in the control group will not receive any intervention during the study; their routine intensive care treatment and care will continue.
The scales will be administered simultaneously with the intervention group at the end of the third day.
|
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 |
|---|---|---|
|
Richards-Campbell Sleep Questionnaire (RCSQ)
時間枠:The sleep questionnaire will be administered upon admission to the intensive care unit on the first day of the study and at the end of the third day of the intervention.
|
The Richard-Campbell Sleep Scale (RCSS) is a scale developed by Richards in 1987 to assess the quality of nocturnal sleep in patients.
Adapted into Turkish by Özlü and Özer, and subsequently validated and its reliability studied, the scale consists of six items that evaluate the depth of nocturnal sleep, time to fall asleep, frequency of awakenings, duration of wakefulness, quality of sleep, and ambient noise level.
Each item is evaluated on a visual analog scale ranging from 0 to 100.
A score of "0-25" indicates very poor sleep, while a score of "76-100" indicates very good sleep.
As the scale score increases, the patients' sleep quality also improves.
The Cronbach's α value of the scale was determined to be 0.82.
|
The sleep questionnaire will be administered upon admission to the intensive care unit on the first day of the study and at the end of the third day of the intervention.
|
|
Hospital Anxiety and Depression Scale (HADS)
時間枠:The scale will be administered as a first test during the initial interview at the beginning of the study and as a final test during the final interview at the end of the third day.
|
Developed by Zigmond and Snaith (1983) to determine a patient's risk of anxiety and depression, and to measure their level and severity, the scale's validity and reliability in Turkish were established by Aydemir et al. (1997).
The scale contains 14 questions in total, with odd numbers measuring anxiety and even numbers measuring depression.
The scale consists of two subscales: Anxiety (HAD-A) and Depression (HAD-D).
In the validity and reliability study, the cutoff score for HAD-A was found to be 10/11, and for HAD-D, 7/8.
Accordingly, scores above these points are considered at risk.
The scale is a four-point Likert type, with a total score ranging from 0 to 42.
|
The scale will be administered as a first test during the initial interview at the beginning of the study and as a final test during the final interview at the end of the third day.
|
協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
便利なリンク
- Karaman Özlü, Z., & Özer, N. (2015). Richard-Campbell Uyku Ölçeği geçerlilik ve güvenirlik çalışması. Türk Uyku Tıbbı Dergisi, 2(2), 29-32
- Aydemir, Ö., Güvenir, T., Küey, L., & Kültür, S. (1997). Hastane Anksiyete ve Depresyon Ölçeği Türkçe formunun geçerlilik ve güvenilirliği. Türk Psikiyatri Dergisi, 8(4), 280-287.
研究記録日
主要日程の研究
研究開始 (推定)
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
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。