- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01432431
Spiritual Care in Improving Quality of Life of Patients, Caregivers, and Hospital Staff
Archstone Spiritual Care Demonstration Project: Outcomes for Patients, Families, and Staff
Studieoversikt
Status
Forhold
Detaljert beskrivelse
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.
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
California
-
Duarte, California, Forente stater, 91010
- City of Hope Medical Center
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: Supportive care (spiritual care)
See Detailed Description.
|
Hjelpestudier
Hjelpestudier
Undergo palliative spiritual care
Andre navn:
Undergo palliative spiritual care
Andre navn:
Undergo palliative spiritual care
Undergo palliative spiritual care
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change over time in number of unduplicated palliative care patients screened for spiritual concerns and spiritual history
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Jay Thomas, City of Hope Medical Center
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 11110 (DAIDS ES Registry Number)
- NCI-2011-02730 (Registeridentifikator: CTRP (Clinical Trial Reporting Program))
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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