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A Thematic Analysis of Compassion Rounds

5. mai 2021 oppdatert av: 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.

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Observasjonsmessig

Registrering (Faktiske)

30

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Florida
      • Orlando, Florida, Forente stater, 32804
        • AdventHealth Orlando

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

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

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
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

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Validated Thematic Framework to Explain the Effects of Compassion Rounding
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Compendium of Evidence-Based Best Practices for the Implementation of Compassion Rounding
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Etterforskere

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

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. oktober 2018

Primær fullføring (Faktiske)

31. juli 2019

Studiet fullført (Faktiske)

28. august 2019

Datoer for studieregistrering

Først innsendt

15. august 2018

Først innsendt som oppfylte QC-kriteriene

23. august 2018

Først lagt ut (Faktiske)

28. august 2018

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. mai 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

5. mai 2021

Sist bekreftet

1. mai 2021

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 1320386

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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