Implementing Spiritual Care in Inpatient Palliative Care (SCPC)

February 9, 2026 updated by: University Hospital Muenster

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

Study Type

Observational

Enrollment (Actual)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North Rhine-Westphalia
      • Münster, North Rhine-Westphalia, Germany, 48149
        • University hospital Muenster

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The study population consists of patients assigned to general and specialized Palliative Care due to justifying indications like progressive malign and non-malign diseases that need inpatient treatment provided by either counselling services or on palliative ward.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
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
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.
6 months
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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Philipp Lenz, Prof. Dr. med., University hospital Muenster

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2023

Primary Completion (Actual)

May 31, 2024

Study Completion (Actual)

December 31, 2024

Study Registration Dates

First Submitted

January 4, 2024

First Submitted That Met QC Criteria

January 4, 2024

First Posted (Actual)

January 16, 2024

Study Record Updates

Last Update Posted (Actual)

February 12, 2026

Last Update Submitted That Met QC Criteria

February 9, 2026

Last Verified

November 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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