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A Thematic Analysis of Compassion Rounds

5 de maio de 2021 atualizado por: AdventHealth

A Thematic Analysis of the Effects of Compassion Rounds on Clinicians and the Families of NICU Patients

The primary objective of this thematic analysis is to understand the experience of "Compassion Rounds" for patients, families, friends, and clinicians. The secondary objective of this study is to evaluate and interpret data to determine best practice recommendations for standardization and scalability.

Visão geral do estudo

Status

Concluído

Condições

Intervenção / Tratamento

Descrição detalhada

This research will be conducted as a Thematic Analysis. Participants will be recruited from those who take part in compassion rounds, including patients, their loved ones, physicians, chaplains, social workers, nurses, and other care providers.

Qualitative data on participants' experiences throughout the intervention will be collected and analyzed using thematic methodology. The data will be used to explain the psychosocial processes that influence participant experience and reported outcomes.

Qualitative methodology does not seek to verify hypotheses based on logical assumptions, as quantitative measures do, instead it is used to derive salient constructs directly from the data. This methodology allows inductive understanding of participants' social reality and perceptions of the treatment, resulting in explanations of how the treatment leads to outcomes and the identification of variables that may then be quantified for more generalizable study.

Semi-structured Interviews

Through semi-structured interviews, which will be recorded and transcribed, the researcher asks participants open-ended questions intended to elicit perspectives on their experience of compassion rounds, without limiting responses to pre-determined categories of interest. The following are examples:

"What/who do you remember most vividly?" "How would you describe your experience to a friend?" "What was most meaningful to you? "What made you feel uncomfortable?" "Would you do it again? Why or why not?" "What, if anything, changed after compassion rounding?"

Coding

The researcher codes and documents throughout data collection and analysis to lend transparency to the coding process and to keep a record of ideas to inform thematic exposition. The researcher assigns categorical codes (labels or concepts) to the transcribed responses line-by-line, analyzing patterns of relationships and using a constant comparison technique to identify similarities and differences throughout the data. The following coding techniques will be used to analyze transcriptions:

  • open coding: the researcher segments the data into preliminary categories, based on similarity
  • axial coding: the researcher groups the categories into themes that provide new ways of seeing and understanding the phenomenon under study
  • selective coding: the researcher integrates the categories and themes to articulate a coherent theory of the phenomenon of study.

Theoretical Sampling Grounded theory research uses "theoretical sampling" to identify participants for interviews. Purposive samples are identified to initiate data collection and analysis, and to select participants who are likely to clarify, verify, or contradict data as it is collected. Sampling concludes when the data is "saturated," which occurs when coded categories are well-defined and no new significant insights are emerging from interviews.

Thematic Development and Validation

The researcher develops thematic explanations that stem from rendering participants' experiences throughout the practice of compassion rounding.

Themes are evaluated for fit and relevance and employee participants may be asked to validate the researcher's findings in follow-up interviews and focus groups.

Observation The researcher will also observe compassion rounding to collect data that will provide further insight to participants' experiences. Observations of interactions and reactions in real time will be documented and the data will be coded and analyzed using the techniques described above. Observational data will not be integrated into interview data, but will be used to confirm or contrast reported data.

Tipo de estudo

Observacional

Inscrição (Real)

30

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

    • Florida
      • Orlando, Florida, Estados Unidos, 32804
        • AdventHealth Orlando

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

Não

Gêneros Elegíveis para o Estudo

Tudo

Método de amostragem

Amostra Não Probabilística

População do estudo

Participants will be recruited from participants in compassion rounding, including patients, their loved ones, physicians, chaplains, social workers, nurses, and other care providers.

Descrição

Inclusion Criteria:

  1. An employee of Florida Hospital or Adventist Health System, or a physician with privileges there, or a patient, or a family or friend who has participated in compassion rounding at a Florida Hospital critical care unit
  2. Over the age of 18
  3. Able to provide informed consent
  4. Must speak and understand English
  5. Willing and able to provide a contact phone number

Exclusion Criteria:

1. Discernible cognitive impairment

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

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
Physicians
interview physicians who have conducted compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Chaplains
interview chaplains who have conducted compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Other Healthcare Providers
interview other healthcare providers who have conducted compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Patients
interview patients who have participated in compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

Patient family members/friends
interview patient's loved ones who have participated with the patient in compassion rounds

Initial interview and potential follow-up interviews and focus group with Florida Hospital employees.

Interview participants in compassion rounds

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Validated Thematic Framework to Explain the Effects of Compassion Rounding
Prazo: five months
Analysis of data collected throughout the study will result in a validated theoretical framework to understand and explain the psychosocial processes that influence participant experience and reported outcomes.
five months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Compendium of Evidence-Based Best Practices for the Implementation of Compassion Rounding
Prazo: five months
Analysis of data collected throughout the study will result in an evidence-based compendium of best practices for the implementation of compassion rounding.
five months

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Kim McManus, Ph.D., FH Center for CREATION Health Research

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 outubro de 2018

Conclusão Primária (Real)

31 de julho de 2019

Conclusão do estudo (Real)

28 de agosto de 2019

Datas de inscrição no estudo

Enviado pela primeira vez

15 de agosto de 2018

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de agosto de 2018

Primeira postagem (Real)

28 de agosto de 2018

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de maio de 2021

Última atualização enviada que atendeu aos critérios de controle de qualidade

5 de maio de 2021

Última verificação

1 de maio de 2021

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 1320386

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 .

Ensaios clínicos em interview

3
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