Spiritual Care in Improving Quality of Life of Patients, Caregivers, and Hospital Staff
Archstone Spiritual Care Demonstration Project: Outcomes for Patients, Families, and Staff
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
OBJECTIVES:
I. To improve the quality of spiritual care provided by palliative care teams. II. To measure the effectiveness of integrating spiritual care recommendations in palliative care at City of Hope (COH) and the impact it has on cancer patients, families, and hospital staff.
OUTLINE:
The expanded psychosocial/spiritual assessment administered by social workers includes a spiritual history and a spiritual needs screening. Social worker knowledge and competence is surveyed at baseline, immediately after the course, and after a bedside chaplain-mentoring process. Inpatient cancer patients' and their caregivers' perceptions about spiritual care is surveyed at baseline prior to the social work curriculum and after the course has been completed and the new psychosocial/spiritual assessment has been implemented. Data collected from patients, family members, and staff includes number of unduplicated palliative care patients screened for spiritual concerns, spiritual history, number and type of spiritual issues, number of referrals to the chaplain, number seen by the chaplain, number of unduplicated palliative care patients with documented spiritual care plan, number of staff development sessions offered and topics, attendance per topic, advance directives, and referrals to hospice.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
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California
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Duarte, California, Stati Uniti, 91010
- City of Hope Medical Center
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-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Admitted during the study quarter
- Admitted >= 5 days
- English speaking
- Alert and able to answer questions
Exclusion Criteria:
- Non-cancer diagnosis
- Previously accrued to study
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Supportive care (spiritual care)
See Detailed Description.
|
Studi accessori
Studi accessori
Undergo palliative spiritual care
Altri nomi:
Undergo palliative spiritual care
Altri nomi:
Undergo palliative spiritual care
Undergo palliative spiritual care
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Change over time in number of unduplicated palliative care patients screened for spiritual concerns and spiritual history
Lasso di tempo: At baseline and quarterly for one year
|
Nonparametric Mann-Whitney University test will be used to test for differences between cohorts of patients and of families at the two different measurement points.
The Wilcoxon paired nonparametric test will be used to test for change over time for staff survey results.
|
At baseline and quarterly for one year
|
|
Change over time in number and type of spiritual issues
Lasso di tempo: At baseline and quarterly for one year
|
Nonparametric Mann-Whitney University test will be used to test for differences between cohorts of patients and of families at the two different measurement points.
The Wilcoxon paired nonparametric test will be used to test for change over time for staff survey results.
|
At baseline and quarterly for one year
|
|
Change over time in number of referrals to the chaplain and number seen by the chaplain
Lasso di tempo: At baseline and quarterly for one year
|
Nonparametric Mann-Whitney University test will be used to test for differences between cohorts of patients and of families at the two different measurement points.
The Wilcoxon paired nonparametric test will be used to test for change over time for staff survey results.
|
At baseline and quarterly for one year
|
|
Change over time in number of unduplicated palliative care patients with documented spiritual care plan
Lasso di tempo: At baseline and quarterly for one year
|
Nonparametric Mann-Whitney University test will be used to test for differences between cohorts of patients and of families at the two different measurement points.
The Wilcoxon paired nonparametric test will be used to test for change over time for staff survey results.
|
At baseline and quarterly for one year
|
|
Change over time in number of staff development sessions offered and topics, attendance per topic, advance directives, and referrals to hospice
Lasso di tempo: At baseline and quarterly for one year
|
Nonparametric Mann-Whitney University test will be used to test for differences between cohorts of patients and of families at the two different measurement points.
The Wilcoxon paired nonparametric test will be used to test for change over time for staff survey results.
|
At baseline and quarterly for one year
|
|
Identification of common themes and patterns that answer the key evaluation questions
Lasso di tempo: At baseline and quarterly for one year
|
Analyzed using Atlas.ti.
coding and analysis.
Qualitative data, e.g., open ended questions, included narrative responses by staff summarized for reporting purposes.
|
At baseline and quarterly for one year
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Jay Thomas, City of Hope Medical Center
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 11110 (DAIDS ES Registry Number)
- NCI-2011-02730 (Identificatore di registro: CTRP (Clinical Trial Reporting Program))
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