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A Thematic Analysis of Compassion Rounds

2021年5月5日 更新者: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.

調査の概要

状態

完了

介入・治療

詳細な説明

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.

研究の種類

観察的

入学 (実際)

30

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Florida
      • Orlando、Florida、アメリカ、32804
        • AdventHealth Orlando

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

サンプリング方法

非確率サンプル

調査対象母集団

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

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
介入・治療
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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Validated Thematic Framework to Explain the Effects of Compassion Rounding
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Compendium of Evidence-Based Best Practices for the Implementation of Compassion Rounding
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Kim McManus, Ph.D.、FH Center for CREATION Health Research

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2018年10月1日

一次修了 (実際)

2019年7月31日

研究の完了 (実際)

2019年8月28日

試験登録日

最初に提出

2018年8月15日

QC基準を満たした最初の提出物

2018年8月23日

最初の投稿 (実際)

2018年8月28日

学習記録の更新

投稿された最後の更新 (実際)

2021年5月6日

QC基準を満たした最後の更新が送信されました

2021年5月5日

最終確認日

2021年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 1320386

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

interviewの臨床試験

3
購読する