Spiritual Care in Improving Quality of Life of Patients, Caregivers, and Hospital Staff
Archstone Spiritual Care Demonstration Project: Outcomes for Patients, Families, and Staff
Przegląd badań
Status
Warunki
Szczegółowy opis
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.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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California
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Duarte, California, Stany Zjednoczone, 91010
- City of Hope Medical Center
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
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
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: Supportive care (spiritual care)
See Detailed Description.
|
Badania pomocnicze
Badania pomocnicze
Undergo palliative spiritual care
Inne nazwy:
Undergo palliative spiritual care
Inne nazwy:
Undergo palliative spiritual care
Undergo palliative spiritual care
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change over time in number of unduplicated palliative care patients screened for spiritual concerns and spiritual history
Ramy czasowe: 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.
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At baseline and quarterly for one year
|
|
Change over time in number and type of spiritual issues
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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.
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At baseline and quarterly for one year
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Główny śledczy: Jay Thomas, City of Hope Medical Center
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 11110 (DAIDS ES Registry Number)
- NCI-2011-02730 (Identyfikator rejestru: CTRP (Clinical Trial Reporting Program))
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