Inforcing Spiritual Care: Enhancing Well-Being and Competency in Psychiatric Nurses

February 3, 2025 updated by: Port Said University

In Forcing Spiritual Care: Enhancing Well-Being and Competency in Psychiatric Nurses

This study was done to evaluate the effectiveness of spiritual care education program in enhancing the well-being and competency of psychiatric nurses.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

After explaining the aim of the study, an official permission from the aforementioned psychiatric institutions will acquired to carry out the study. In order to prevent conflicts with regular hospital nursing shifts, the study team had arranged the instructional sessions with the head of nurses. Nursing who fulfilled the qualifying requirements and gave their verbal, informed consent was taken by the researchers. Nurses completed the self-administered data collection sheet. The self-administered questionnaire was completed in 15-20 minutes on average. The pre-test questionnaire was first given to both groups prior to the start of the educational session in order to gather data. The post-test was administered using the same pretest questionnaire.

Intervention of spiritual care education/training program For eight weeks, the intervention group participated in a spiritual care education program that aimed to improve their ability to provide spiritual care. Program orientation, an introduction to spiritual care, the concepts of spiritual care, the significance of spiritual care, the theoretical underpinnings of spirituality in mental health, practical strategies for integrating spiritual care in psychiatric nursing, reflective practice, and self-care for enhancing personal spirituality were all covered in the program's weekly two-hour sessions. Throughout the study period, the control group received no intervention and carried on with their regular nursing practice without any further instruction.

The baseline (pre-intervention) questionnaire was given simultaneously to the intervention and control groups in order to gather data at two different times. A questionnaire measuring spiritual well-being and spiritual care competency was filled out by both groups. The filled surveys were gathered by the study team. Both the intervention and control groups received the immediately post-intervention questionnaire simultaneously, right after the educational program concluded.

Study Type

Interventional

Enrollment (Estimated)

98

Phase

  • Not Applicable

Contacts and Locations

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

Study Contact

Study Locations

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

The participants of this study were 98 psychiatric nurses working in previously mentioned psychiatric settings and who fulfilled the following inclusion criteria as both male and female, had one year of experience in psychiatric care, willingness to participate in the study and provide informed consent and did not enroll in any ongoing spiritual care-related training.

Exclusion Criteria:

Nurses refused to participate Nurses not on the full duty

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

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
The control group will not receive the spiritual care education program
Experimental: Intervention
For eight weeks, the intervention group will participate in a spiritual care education program that aimed to improve their ability to provide spiritual care.
The spiritual care education program to improve nurses ability to provide spiritual care. Education includes; Program orientation, an introduction to spiritual care, the concepts of spiritual care, the significance of spiritual care, the theoretical underpinnings of spirituality in mental health, practical strategies for integrating spiritual care in psychiatric nursing, reflective practice, and self-care for enhancing personal spirituality were all covered in the program's weekly two-hour sessions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Spiritual Care Competence
Time Frame: 8 weeks

The scale was used to evaluate spiritual care competencies. The scale was created and validated in English by Van Leeuwen, Tiesinga, Middel, Post, and Jochemsen (2009). It consists of 27 items total, with six subscales. The scale assesses the following six spiritual-care competencies: communication (2 items), professionalization and improving the quality of care (6 items), personal support and counselling of patients (6 items), referral to other professionals (3 items), attitudes towards patients' spirituality (4 items), and assessment and implementation of SC (6 items).

There are five points ratings on the Likert scale: strongly disagree, disagree, neutral, agree, and strongly agree. Higher scores indicate higher levels of competence; the total score goes from 27 to 135. The subscales demonstrated good homogeneity with average inter-item correlations >0·25 and strong test-retest reliability. Cronbach's α values for the subdimensions of SC assessment and implementation, professiona

8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Spiritual Well-Being
Time Frame: 8 weeks

The Spiritual Well-Being Scale (SWBS) used to measure self-perceived spiritual health. The scale was developed by Ellison and Paloutzian in 1982. The 20-item scale was split into two subscales: existential well-being (EWB), which focused on life satisfaction without necessarily being connected to religion, and had 10 items. Religious well-being (RWB), which reflected a sense of fulfilment and connection with God or a higher power and had 10 items.

The scale is a 6-point Likert scale with 9 negatively worded items to reduce response biases, ranging from Strongly Disagree to Strongly Agree. Higher scores indicate better spiritual well-being; the scale's total scores range from 20 to 120. Three levels have been established for the SWBS scores: low (20 to 40), moderate (41 to 99), and high (100 to 120). High levels of test-retest reliability and internal consistency were demonstrated by the scale. Cronbach's alpha α = 0.87, 0.78, and 0.89 for the RWB, EWB, and SWBS, respectively, indicat

8 weeks

Collaborators and Investigators

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

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 (Estimated)

February 10, 2025

Primary Completion (Estimated)

February 28, 2025

Study Completion (Estimated)

March 1, 2025

Study Registration Dates

First Submitted

February 3, 2025

First Submitted That Met QC Criteria

February 3, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 3, 2025

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Du Rec no 46

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

product manufactured in and exported from the U.S.

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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