- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03648866
A Thematic Analysis of Compassion Rounds
A Thematic Analysis of the Effects of Compassion Rounds on Clinicians and the Families of NICU Patients
Aperçu de l'étude
Description détaillée
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.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
-
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Florida
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Orlando, Florida, États-Unis, 32804
- AdventHealth Orlando
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- 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
- Over the age of 18
- Able to provide informed consent
- Must speak and understand English
- Willing and able to provide a contact phone number
Exclusion Criteria:
1. Discernible cognitive impairment
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
---|---|
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 |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Validated Thematic Framework to Explain the Effects of Compassion Rounding
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Compendium of Evidence-Based Best Practices for the Implementation of Compassion Rounding
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Kim McManus, Ph.D., FH Center for CREATION Health Research
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 1320386
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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