- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06206551
Implementing Spiritual Care in Inpatient Palliative Care (SCPC)
The goal of this observational study is to is to ascertain the spiritual needs of palliative patients in a standardized manner using the Spiritual Needs Questionnaire and to promptly address those needs by (specialized) spiritual care.
To determine whether the effort of implementing the Spiritual Needs Questionnaire on a sustainable basis on the one hand brings the expected benefit to the patients and on the other hand can be provided by the pastoral care personnel, at Muenster University Hospital (specialized) spiritual care interventions will be documented in detail and retrospectively and prospectively collected data will be compared.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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North Rhine-Westphalia
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Münster, North Rhine-Westphalia, Germany, 48149
- University hospital Muenster
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
All individual indication for general and specialised Palliative Care in clinical setting/routine (e.g.):
- Progressive, malign tumours
- Progressive, chronic obstructive pulmonary disease
- Patients with progressive disease and limited life expectancy (< ca. 12 months)
- Patients attended by Palliative Caregivers in counselling services or on palliative ward
- Life expectancy > 2 weeks
- Sufficient comprehension of German language and writing that allows an autonomous or supported completion of the questionnaire.
- Existence of an independently signed written consent.
Exclusion Criteria:
- Severe cognitive impairment
- capacity for consent lacking or impaired
- impaired comprehension of German language and writing that would not allow an autonomous or supported completion of the questionnaire.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Prospective patients
Patients who are on the palliative care ward or who are being treated by the palliative consultation service at the University Hospital Muenster.
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This questionnaire captures the spiritual needs of patients and is used in its short version (screener).This questionnaire is used as part of standard treatment for all palliative care inpatients.
|
|
Restrospective patients
Patients who were on the palliative care ward or were treated by the palliative consultation service at University Hospital Muenster during the same period in the previous year.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of standardized and evidence-based recordation and implementation of Spiritual Care in Palliative Care
Time Frame: 6 months
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Feasibility of standardized and evidence-based recordation and implementation of Spiritual Care in Palliative Care based on the number of interventions provided by general and/or specialized Spiritual Care for patients with ascertained needs detected by the validated Spiritual Needs Questionnaire in German language.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Recordation of needs for general / specialized spiritual care in palliative care
Time Frame: 6 months
|
Recordation of needs for general / specialized spiritual care in palliative care consultation service and palliative ward of a university tertiary care hospital.
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6 months
|
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Differences in use and outcomes comparing standardised and non-standardised evaluation of spiritual care needs (comparison with retrospective data).
Time Frame: 6 months
|
s. title
|
6 months
|
|
Examination of further descriptive and analysing comparisons of retrospective data and intervention group.
Time Frame: 6 months
|
s. title
|
6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Philipp Lenz, Prof. Dr. med., University hospital Muenster
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Nervous System Diseases
- Cardiovascular Diseases
- Pathologic Processes
- Heart Diseases
- Neuromuscular Diseases
- Chronic Disease
- Disease Attributes
- Respiratory Tract Diseases
- Lung Diseases
- Lung Diseases, Obstructive
- Neurodegenerative Diseases
- Pathological Conditions, Signs and Symptoms
- Neoplasms
- Heart Failure
- Pulmonary Disease, Chronic Obstructive
- Motor Neuron Disease
Other Study ID Numbers
- 2023-465-b-S
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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