Music Listenıng And Training Before Coronary Angıography
20 de abril de 2022 actualizado por: 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.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
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.
Tipo de estudio
Intervencionista
Inscripción (Actual)
102
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Merkez
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Bolu, Merkez, Pavo, 14100_
- Abant Izzet Baysal University
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Todos
Descripción
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 de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: 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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Experimental: 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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Sin intervención: 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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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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means of subjective anxiety scores
Periodo de tiempo: 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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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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means of subjective pain scores
Periodo de tiempo: up to 45 minutes
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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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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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means of blood pressure (mmHg)
Periodo de tiempo: 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)
Periodo de tiempo: up to 45 minutes
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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)
Periodo de tiempo: 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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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
1 de abril de 2018
Finalización primaria (Actual)
1 de abril de 2019
Finalización del estudio (Actual)
1 de abril de 2019
Fechas de registro del estudio
Enviado por primera vez
26 de junio de 2020
Primero enviado que cumplió con los criterios de control de calidad
25 de noviembre de 2020
Publicado por primera vez (Actual)
3 de diciembre de 2020
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
21 de abril de 2022
Última actualización enviada que cumplió con los criterios de control de calidad
20 de abril de 2022
Última verificación
1 de abril de 2022
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- AIBU-HSF-AYN-01
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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