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Effect of Innovative Thinking Development Program on Some Approaches of Nursing Students

1 de abril de 2021 atualizado por: Ilknur Aydin Avci, Ondokuz Mayıs University

Effect of The Innovatıve Thınkıng Development Program on The Innovatıve Approaches, Crıtıcal Thınkıng and Perceıved Competence of Nursıng Students

Background: This study was conducted to determine the effect of the Innovative Thinking Development Program (ITDP) on the innovative approaches, critical thinking and perceived competence of nursing students.The study has a non-randomized, control group pre-test-post-test experimental research design. The study population consisted of senior students in the Nursing Department of two similar faculties in the academic calendar 2019-2020 (n=164). In the study, the ITDB developed by the researcher was applied to the students in the experimental group. The research data were collected online using a 'Personal Information Form', 'Individual Innovativeness Scale', 'Marmara Critical Thinking Trends Scale', 'Self-Efficacy Scale' and 'Success Test 'developed by the researcher. Independent samples t test, Kruskal Wallis, Wilcoxon, ANOVA tests were used in the analysis of the data. Institutional permissions and ethics committee approval was obtained for the research.

Hypothesis:

H0: The innovative approaches, critical thinking tendencies and competence perceptions of nursing students included in ITDP do not change.

H1: Individual innovativeness, critical thinking disposition and self-efficacy scale scores of nursing students in the experimental group will change after ITDP.

Visão geral do estudo

Descrição detalhada

This study was conducted to determine the effect of the ITDP on the innovative approaches, critical thinking and perceived competence of nursing students.The non randomized clinical trial was based on the guidelines proposed by the Consolidated standard of Reporting Trials- CONSORT 2010. The data of the research were collected in Giresun and Ordu University Health Science Faculty between April 2020- October 2020.

In this study, there is a non-randomized experimental group and two control groups (total 164 nursing students). Experimental and control groups were determined by lots. Data collected through online forms.

The developed educational program was implemented to students in the experimental group through an online platform. The trainings lasted 6 weeks and different applications were made with themes appropriate to the content. In addition, a whatsapp group was opened and posts about innovation thinking exercises were made.

The research data were collected a 'Personal Information Form', 'Individual Innovativeness Scale', 'Marmara Critical Thinking Trends Scale' and 'Self-Efficacy Scale' in pre test and post tests.The efficiency of the program was determined by applying an 'Success Test' to the experimental group.

Personal Information Form: The twenty-one question 'Personal Information Form' consists of sociodemographic questions and questions related to innovation.

Individual Innovation Scale (IIS): The scale was developed in 1977. The scale was adapted to Turkish in 2014. The scale adapted to nursing is 5-point Likert type. It consists of three sub-dimensions and a total of 18 questions. These sub dimensions are; resistance to change sub-dimension, opinion leadership sub-dimension and risk-taking sub-dimension. According to the score obtained from the scale; Scores of 57 and below are classified as 'traditionalist', those who score between 58-65 as 'skeptical', those who score between 66 and 74 as 'questioning', those who score between 75 and 82 as 'pioneer', and those who score 82 and above as 'innovative'. Scale Cronbach Alpha value is 0.82. The Cronbach Alpha value of the scale for this study is 0.94.

Marmara Critical Thinking Trends Scale (MCTTS): The scale was developed in 2018. The scale consists of 28 items and 6 sub-dimensions. The scale is in 5-point Likert type. Scale sub-dimensions; reasoning, reaching judgment, searching for evidence, searching for truth, open-mindedness and systematicity. The high score obtained from each sub-dimension of the scale indicates that the individual has the feature in the relevant sub-dimension. Scale Cronbach Alpha value is 0.91. The Cronbach Alpha value of the scale for this study is 0.93.

Self-Efficacy Scale (SES):The scale was developed in 1983.The scale was adapted to Turkish in 1999. It is a 5-point Likert type consisting of 23 items. The 4 sub-dimensions of the scale are starting behavior, maintaining behavior, completing behavior and struggling with obstacles. The high total score obtained from the scale indicates that the general efficacy perception is high, and the low general efficacy perception is low. Scale Cronbach Alpha value is 0.81. The Cronbach Alpha value of the scale for this study is 0.88.

Evaluation of Data SPSS 23.0 statistical package program was used for statistical analysis and evaluation of the data. Whether the data showed normal distribution was checked with the Kolmogorov-Smirnov test. Independent samples t test and Mann Whitney U test were used to compare data between groups according to normality test. Paired samples t test and Wilcoxon test were used to compare the pre-test and post-test values within the group. The Chi-square test and two ratio tests were used to analyze categorical data. Significance level was taken as p <0.05.

Information:

No budget was received from any institution for the research. Ethics committee approval was obtained and verbal consent was obtained from the participants.

There is no conflict of interest.

Tipo de estudo

Intervencional

Inscrição (Real)

164

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

    • Atakum
      • Samsun, Atakum, Peru, 55200
        • Ondokuz Mayıs 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

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Volunteering to participate in the study,
  • Being open to communication,
  • Being a fourth year nursing student,
  • Not to be an innovation and entrepreneurship course in the curriculum,
  • Students have online access opportunities.

Exclusion Criteria:

  • Not being willing to participate in the study,
  • Not being open to communication,
  • Not being a fourth year nursing student,
  • To come by undergraduate transfer and to have taken innovation and entrepreneurship course at the faculty he came from,
  • Students do not have online access facilities.

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: Outro
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Intervention Group
After determining the experimental and control groups, pre-tests were performed.The program was applied to students in the experimental group.The program was implemented for six weeks based on the theme of innovative thinking.The program developed a training program based on the Tyler Taba model. This model, which is often used in developing educational programs, includes all the necessary steps to teach and accept a new concept. In the ITDP training program, an interactive educational content has been created in which knowledge will be transformed into behavior.In the training, subjects were taught in units, workshops were held, seminars were given. Post-tests were applied at the end of the training.
With the implementation of the program, nursing students are expected to develop innovative thinking skills.
Sem intervenção: Control Group I
Pre-test and post-tests were applied to the non-intervention group
Sem intervenção: Control Group II
Pre-test and post-tests were applied to the non-intervention group

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Individual Innovativeness Scale
Prazo: 3 months
The scale measures individual innovativeness level. The lowest 18 points on the scale and 90 points are the highest. Based on the score obtained from the scale; 57 points and six fields 'traditionalist', 58-65 points to the areas between the 'skeptic', 66-74 score between 'questioner', 75-82 score between 'pioneer', those who scored above 82 points and 'innovative' are classified as.The increase in the scores obtained from the scale shows that the people are innovative.
3 months
Critical Thinking Trends Scale
Prazo: 3 months
The scale measures people's tendency to think critically. A high score taken from each sub-dimension indicates that the individual has a characteristic of the corresponding sub-dimension, and a total critical thinking trends score is obtained from the scale. The higher the score, the higher the critical thinking disposition.The highest score on the scale is 140.
3 months
Self-Efficacy Scale
Prazo: 3 months
This scale is used to measure people's perceptions of competence. Scores between 23 and 115 can be obtained from the scale. A high overall score on the scale indicates that people's overall perception of competence is high, and a low overall perception of competence is low.
3 months
Success Test
Prazo: 3 months
The test, developed in accordance with innovative thinking skills, consists of 20 questions.The highest 20 points and the lowest 0 points are taken from this test. The higher the score, the higher the innovative thinking.This test was developed to test the effectiveness of the training program on innovative thinking and to evaluate students' success on this subject. Pre-test was applied to the experimental group as post-test.
3 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Diretor de estudo: İlknur Aydın Avcı, Prof, Ondokuz Mayıs University

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)

15 de dezembro de 2019

Conclusão Primária (Real)

15 de dezembro de 2020

Conclusão do estudo (Real)

1 de fevereiro de 2021

Datas de inscrição no estudo

Enviado pela primeira vez

3 de fevereiro de 2021

Enviado pela primeira vez que atendeu aos critérios de CQ

3 de fevereiro de 2021

Primeira postagem (Real)

8 de fevereiro de 2021

Atualizações de registro de estudo

Última Atualização Postada (Real)

5 de abril de 2021

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de abril de 2021

Última verificação

1 de abril de 2021

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2019/340

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

The data are not publicly available due to their containing information that could compromise the privacy of research. However, authors on the subject can be reached.

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 .

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