The Impact of Multimedia Psychological Support Platform and Acceptance and Commitment Therapy Workshops of Oncology Nurses

January 16, 2025 updated by: National Taiwan University Hospital

The Impact of Multimedia Psychological Support Platform and Acceptance and Commitment Therapy Workshops on the Mental and Physical State of Oncology Nurses

Based on the high levels of emotional distress, burnout, and turnover intentions among clinical oncology nursing staff, this study will provide a multimedia "Mind-Body Support" Line platform and ACT workshop courses as intervention measures for oncology nursing staff. The study aims to explore the effectiveness of these interventions in alleviating their psychological and physical distress, utilizing both qualitative and quantitative research methods to achieve the research objectives.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

100

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

  • Name: Yun-Hsiang Lee Associate Professor, PhD
  • Phone Number: +886 978082338
  • Email: yhlee338@ntu.edu.tw

Study Locations

  • Taiwan
      • Taipei, Taiwan, 802
        • Recruiting
        • National Taiwan University Hospital
        • Contact:

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

Yes

Description

Inclusion Criteria:

  • Currently working as an oncology nurse in a clinical setting

Exclusion Criteria:

  • "Unwilling or unable to participate in the full training course"

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Intervention Group
After attending a 4-hour ACT workshop, participants will utilize the remaining course time to independently access the LINE platform. The platform will feature pre-recorded guided audio files for relaxation, emotional videos, and psychological cards.
Other: Intervention Group
Attending a 4-hour ACT workshop, and after attending participants will utilize the remaining course time to independently access the LINE platform. The platform will feature pre-recorded guided audio files for relaxation, emotional videos, and psychological cards.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychological flexibility
Time Frame: Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.
We utilized the Work-related Acceptance and Action Questionnaire (WAAQ) as the primary outcome measure. This scale assesses psychological resilience in the workplace and comprises 7 items, each rated on a 7-point Likert scale. A score of 1 indicates that the described situation never applies, while a score of 7 indicates it always applies. Total scores range from 7 to 49, with higher scores indicating greater levels of work-related psychological resilience.
Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical and Physical State
Time Frame: Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.
We use the Single Item Fatigue Scale, scored on a Numerical Rating Scale (0-10), where 0 indicates no fatigue and 10 indicates extreme fatigue. This scale measures oncology nurses' subjective fatigue levels on the assessment day, with higher scores reflecting greater fatigue.
Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.
Physical and Physical State
Time Frame: Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.
We use the Depression, Anxiety, and Stress Scale - 21 Items (DASS-21) for measurement. The scale consists of 21 items, each rated on a 4-point Likert scale, where 0 indicates the symptom never applies and 3 indicates it applies most of the time or very much. Higher scores reflect greater severity of the symptoms.
Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.
Physical and Physical State
Time Frame: Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.
We use the Nurses' Intent to Resign Scale, which consists of 14 items rated on a 5-point Likert scale. A score of 1 indicates the statement never applies, while a score of 5 indicates it applies to a great extent. Higher scores reflect a greater intent to resign.
Measurements will be taken before the workshop intervention, immediately after the workshop intervention, and one month later.

Collaborators and Investigators

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

Sponsor

National Taiwan University Hospital

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 6, 2024

Primary Completion (Estimated)

July 31, 2025

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

December 5, 2024

First Submitted That Met QC Criteria

January 16, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 16, 2025

Last Verified

December 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 202411009RIND

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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