A Culturally Specific End-of-life Communication Skills Training

Sponsor
The Hong Kong Polytechnic University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05888480
Collaborator
(none)
148
2
5

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to evaluate the effectiveness of culturally specific end-of-life communication skills training (CST) among Chinese oncology nurses.

The main question it aims to answer is: What is the effectiveness of culturally specific end-of-life CST among Chinese oncology nurses? Participants will receive an 8-week communication skills training. Researchers will compare the intervention group and the wait-list group to see if skills, self-efficacy, and outcome expectancy beliefs will be improved.

Condition or Disease Intervention/Treatment Phase
  • Other: The end-of-life communication skills training
  • Other: Routine training activity
N/A

Detailed Description

Objectives: The study aims to evaluate the effectiveness of culturally specific end-of-life CST among Chinese oncology nurses.

Design and participants: It is designed as a single-blind, pre-post randomized controlled trial (RCT). Registered nurses who work with advanced cancer patients in hospital settings will be recruited. The participants will be randomly assigned to either the intervention group (IG) or the control group (CG). The IG will receive the end-of-life CST between the two measurement points, and the CG will be a waitlist group and receive the training after the end of data collection.

Data analysis: Demographic information about the participants will be summarised in descriptive statistics. Independent t-tests and chi-square tests are used to investigate the comparability of groups in terms of the demographics generated by randomization. The primary and secondary outcome variables will be examined using covariate-adjusted linear mixed models. This approach enables the consideration of missing data. For non-repeated continuous measurements, ordinary linear regression and logistic models will be adopted. The intention-to-treat (ITT) analysis and post hoc analyses of contaminated data will be performed.

Expected results: Nurses' skills, self-efficacy, and outcome expectancy beliefs will improve after the CST.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
148 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Intervention Model Description:
The IG will receive the end-of-life CST between the two measurement points, and the CG will be a waitlist group and receive the training after the end of data collection.The IG will receive the end-of-life CST between the two measurement points, and the CG will be a waitlist group and receive the training after the end of data collection.
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Effects of a Culturally Specific End-of-life Communication Skills Training for Chinese Oncology Nurses
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group (IG)

The IG will receive the end-of-life CST between the two measurement points

Other: The end-of-life communication skills training
Training methods include lectures, video demonstrations, and simulation in small groups (4-5 trainees per group with multidisciplinary roles). Written and audiovisual learning materials will be offered. Each session will be 150 minutes, including lectures and video demonstration (90 min/session) and simulation and feedback (60 min/session). One session will be conducted in two weeks. Totally there will be four sessions completed in 8 weeks.

Other: Control group (CG)

The CG will be a waitlist group and receive the training after the end of data collection.

Other: Routine training activity
Routine training activities arranged by relevant departments in hospitals

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline Skills at 3 months [up to 3 months]

    Measured by Nurses' Clinic Communication Competency Scale, a 58-item self-reported scale which measures six dimensions. A 5-point Likert scale from (1) very poor to (5) very good is used. Higher scores mean a better outcome.

Secondary Outcome Measures

  1. Change from Baseline Self-efficacy at 3 months [up to 3 months]

    Measured by Hospice Care Self-efficacy Scale on nurses, a 12 items with a 5-point Likert scale from (1) very diffident to (5) very confident. Higher scores mean a better outcome.

  2. Change from Baseline Outcome expectancy beliefs 3 months [up to 3 months]

    Measured by The Communication Outcomes Questionnaire, a 23-item self-report questionnaire with a 9-point Likert scale from 1 = very likely and 9 = very unlikely. Higher scores mean a worse outcome.

Other Outcome Measures

  1. Acceptance and satisfaction [up to 3 months]

    Self-developed items and open questions anout the training experience

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Registered nurses who work with advanced cancer patients in hospital settings

  • Consent to participate in the study

Exclusion Criteria:
  • Nurses working temporarily in the two hospitals as scholars or trainees from other hospitals

  • Specialized nurses in palliative care

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • The Hong Kong Polytechnic University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr Joyce Chung, Assistant Professor, School of Nursing, The Hong Kong Polytechnic University
ClinicalTrials.gov Identifier:
NCT05888480
Other Study ID Numbers:
  • HSEARS20230525002
First Posted:
Jun 5, 2023
Last Update Posted:
Jun 5, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr Joyce Chung, Assistant Professor, School of Nursing, The Hong Kong Polytechnic University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 5, 2023