Music Listenıng And Training Before Coronary Angıography
20 avril 2022 mis à jour par: Abant Izzet Baysal University
Effects On Physıological Parameters And Anxiety Of Related Musıc And Informatıon Training Before Coronary Angiography
The aim of this study was to investigate the effects of education and music listening on the anxiety and physiological parameters experienced by individuals undergoing elective coronary angiography.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
The aim of this study was to investigate the effects of education and music listening on the anxiety and physiological parameters experienced by individuals undergoing elective coronary angiography.
The population of the study consisted of individuals undergoing elective coronary angiography in the Cardiology Department of Abant İzzet Baysal University İzzet Baysal Training and Research Hospital. The study was conducted in a randomized controlled manner with three groups: 34 individuals in music listening group (M1), 34 individuals in information training group (M2) and 34 subjects in control group. In order to collect data, CAG (Coronary angiography) Procedure Training Form, Patient Identification Form, Physiological Parameters Form and Visual Analogue Scale and Spielberg State and Trait Anxiety Scale were used. Data were collected by face to face interview technique. Descriptive statistics, Independet Simple test, Paired sample t test, Kruskall Wallis, Mann Whitney U test and Wilcoxon signed rank test were used in the analysis of the data and the significance level was accepted as p <0.05.
Type d'étude
Interventionnel
Inscription (Réel)
102
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Merkez
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Bolu, Merkez, Turquie, 14100_
- Abant Izzet Baysal University
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
Applying femoral CAG electively,
- The first time CAG will be held,
- Performing the CAG procedure for diagnostic purposes,
- Not trained on the CAG process,
- Volunteering to participate in the study,
- No problem in verbal communication,
- No hearing loss,
- Being able to read and write,
- Has not been diagnosed with psychiatric illness,
- Being conscious,
- Being 18 or older.
Exclusion Criteria:
Radial application of CAG,
- Previously performing coronary angiography,
- Performing the CAG procedure for therapeutic purposes (stent, balloon, etc.),
- Having received training on the KAG process,
- Does not want to participate in the study
- Problems in verbal communication,
- Hearing loss,
- Psychiatric illness is found.
- Consciousness is closed.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: music theraphy
One of the 4 music genres (Turkish Folk, Classical, Turkish Art and Sufi Music), which was determined by the researcher by scanning the literature 30 minutes before the CAG procedure, and the expert opinion was taken to the participants in this group was played with a 5-minute headset.
The musical genres were arranged in instrumental, nonverbal, 70 decibels in terms of rhythm and duration and played according to the individual's choice.
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The music selected by the participants was played to the music listening group.
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Expérimental: information education
Participants in this group were trained to inform them about CAG in visual, audio and written form.
Information training was provided by the researcher 30 minutes before the CAG procedure after the outpatient clinic controls of the patient.
Information education prepared by the researcher by scanning the literature and getting expert opinion; It includes 7 minutes of video explanation about the CAG process, discussion after video watching, question and answer, and the delivery of a training book prepared in written form.
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Individual training group was trained on coronary angiography.
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Aucune intervention: nursing care
Individuals in this group received routine nursing care and no intervention was made by the researcher.
In routine nursing care for individuals who will receive CAG procedure in the clinic; Preparation for the CAG procedure, which involves opening the vascular access and dressing the surgical gown, is included in the pre-and post-procedure routine once and more frequently when there are deviations from normal, and if the patient asks questions about the procedure, measurement of blood pressure, heart rate and oxygen saturation.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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means of subjective anxiety scores
Délai: up to 45 minutes
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Spielberg State- Trait Anxiety Scale.
The total score between 0-19 obtained from the state anxiety scale shows that there is no anxiety, the total score between 20-39 indicates mild, the average score between 40-59 indicates moderate, and the total score between 60-79 indicates severe anxiety, and over 60 points are needed for professional help.
The scores obtained from the trait anxiety scale vary between 20 and 80.
A high score means a high and a low level means anxiety.
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up to 45 minutes
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
means of subjective pain scores
Délai: up to 45 minutes
|
visual analog scale.
It consists of a straight line with endpoints that define end limits such as "no pain" and "pain as bad as possible".
The patient is asked to mark the level of pain on the line between the two endpoints.
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up to 45 minutes
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Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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means of blood pressure (mmHg)
Délai: up to 45 minutes
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In the study, a digital sphygmomanometer, which has been calibrated in comparison with the mercury sphygmomanometer, is used in order to prevent individual differences in the measurement of blood pressure.
For accurate results, the sphygmomanometer sleeve is sized for adult individuals (width = about 20 cm, length = about 40 cm).
In order for the blood pressure not to be affected by the conditions during the measurement, it is taken into account that the individual did not drink tea or coffee, take caffeine, and preferably did not eat during the 30 minutes prior to measurement.
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up to 45 minutes
|
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means of heart rate (/min)
Délai: up to 45 minutes
|
The heart rate is the pressure of the left ventricle on the vascular wall of the blood that it throws into the aorta during systole from the skin surface.In the research, radial heart rate is measured as manuel.
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up to 45 minutes
|
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means of respiratory rate (/min)
Délai: up to 45 minutes
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The respiratory rate is the patient's breath per minute.
In this study, respiratory rate was counted by monitoring chest movements for one minute while the patient was in a sitting position.
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up to 45 minutes
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Collaborateurs et enquêteurs
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Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
1 avril 2018
Achèvement primaire (Réel)
1 avril 2019
Achèvement de l'étude (Réel)
1 avril 2019
Dates d'inscription aux études
Première soumission
26 juin 2020
Première soumission répondant aux critères de contrôle qualité
25 novembre 2020
Première publication (Réel)
3 décembre 2020
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
21 avril 2022
Dernière mise à jour soumise répondant aux critères de contrôle qualité
20 avril 2022
Dernière vérification
1 avril 2022
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- AIBU-HSF-AYN-01
Plan pour les données individuelles des participants (IPD)
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NON
Informations sur les médicaments et les dispositifs, documents d'étude
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