Music Listenıng And Training Before Coronary Angıography
20 de abril de 2022 atualizado 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.
Visão geral do estudo
Status
Concluído
Condições
Intervenção / Tratamento
Descrição detalhada
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 estudo
Intervencional
Inscrição (Real)
102
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
-
-
Merkez
-
Bolu, Merkez, Peru, 14100_
- Abant Izzet Baysal University
-
-
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
18 anos e mais velhos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Sim
Gêneros Elegíveis para o Estudo
Tudo
Descrição
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.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Cuidados de suporte
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
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.
|
The music selected by the participants was played to the music listening group.
|
|
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.
|
Individual training group was trained on coronary angiography.
|
|
Sem intervenção: 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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
means of subjective anxiety scores
Prazo: up to 45 minutes
|
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.
|
up to 45 minutes
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
means of subjective pain scores
Prazo: 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.
|
up to 45 minutes
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
means of blood pressure (mmHg)
Prazo: up to 45 minutes
|
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.
|
up to 45 minutes
|
|
means of heart rate (/min)
Prazo: 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.
|
up to 45 minutes
|
|
means of respiratory rate (/min)
Prazo: up to 45 minutes
|
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.
|
up to 45 minutes
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
1 de abril de 2018
Conclusão Primária (Real)
1 de abril de 2019
Conclusão do estudo (Real)
1 de abril de 2019
Datas de inscrição no estudo
Enviado pela primeira vez
26 de junho de 2020
Enviado pela primeira vez que atendeu aos critérios de CQ
25 de novembro de 2020
Primeira postagem (Real)
3 de dezembro de 2020
Atualizações de registro de estudo
Última Atualização Postada (Real)
21 de abril de 2022
Última atualização enviada que atendeu aos critérios de controle de qualidade
20 de abril de 2022
Última verificação
1 de abril de 2022
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- AIBU-HSF-AYN-01
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .