- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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
Study Overview
Status
Conditions
Detailed Description
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Duarte, California, United States, 91010
- City of Hope Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Supportive care (spiritual care)
See Detailed Description.
|
Ancillary studies
Ancillary studies
Undergo palliative spiritual care
Other Names:
Undergo palliative spiritual care
Other Names:
Undergo palliative spiritual care
Undergo palliative spiritual care
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change over time in number of unduplicated palliative care patients screened for spiritual concerns and spiritual history
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: 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
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Jay Thomas, City of Hope Medical Center
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11110 (DAIDS ES Registry Number)
- NCI-2011-02730 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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