Clinical Trial: Re-evaluation of the Feasibility and Acceptability of a Web-based Educational Program to Improve Nurses' Ability to Assess Cancer Cachexia (Japan)

Tokyo, July 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061519) titled 'Re-evaluation of the Feasibility and Acceptability of a Web-based Educational Program to Improve Nurses' Ability to Assess Cancer Cachexia' on June 30.

Study Type: Interventional

Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - St. Luke's International University

Condition: Condition - Nurses involved in the care of patients with advanced cancer who are undergoing cancer drug therapy. Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The purpose of this study is to reevaluate the feasibility and acceptability of a nursing education program that provides basic knowledge of cancer cachexia and strategies for comprehensive assessment of cancer cachexia. Basic objectives2 - Safety

Intervention: Interventions/Control_1 - The participants will take the cancer cachexia nursing education program (e-learning) in two weeks.

Eligibility: Age-lower limit - 18 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - 1) Nurses working at designated cancer care hospitals in Japan. 2) Nurses involved in the care of patients with advanced cancer who are undergoing cancer drug therapy. 3) Nurses with 10 years or less of clinical experience as a nurse. 4) Individuals with sufficient ability to understand written Japanese. 5) Individuals aged 18 years or older at the time of consent. 6) Individuals who provide informed consent to participate in this study via Google Forms. Key exclusion criteria - 1) Individuals who participated in previous studies: A Web-based Educational Program to Improve Nurses' Ability to Assess Cancer Cachexia: A Pilot Randomized Controlled Trial. 2) Individuals in managerial positions who are not directly involved in patient care. 3) Individuals judged by the principal investigator or co-investigators to be unsuitable for participation in this study. Target Size - 10

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 05 Month 11 Day Anticipated trial start date - 2026 Year 07 Month 01 Day Last follow-up date - 2026 Year 09 Month 30 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070393

Disclaimer: Curated by HT Syndication.