Viewing Study NCT06366685



Ignite Creation Date: 2024-05-06 @ 8:24 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06366685
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-16
First Post: 2024-04-06

Brief Title: Development and Initial Application of a Combined Exercise and Psychological Intervention Program for Patients After Esophagectomy
Sponsor: Mengmeng Yuan
Organization: Anhui Medical University

Study Overview

Official Title: Development and Initial Application of a Combined Exercise and Psychological Intervention Program for Patients After Esophagectomy
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: Recovery
Brief Summary: Esophageal cancer imposes a significant burden in China accounting for over 60 of the global disease burden While surgery remains a common and highly effective treatment for esophageal cancer patients often experience multiple physical and psychological symptoms postoperatively severely affecting their recovery outcomes and quality of life Although existing exercise or psychological intervention programs have shown some effectiveness issues such as relatively singular intervention content imprecise intervention timing and vague intervention details persist

This project based on previous research foundations including the development of symptom measurement tools and the identification of key recovery periods is guided by symptom management theory and knowledge translation models Taking a perspective of the synergistic impact of physical and psychological symptoms the study focuses on patients undergoing esophageal cancer surgery Initially evidence-based literature review focus group interviews and expert consultations were conducted to develop a combined exercise and psychological intervention program integrating subjective CSCA_EC and objective 6MWT measurement indicators named Recovery For EC Subsequently the program was preliminarily applied in clinical settings using a mixed-methods approach combining quantitative quasi-experimental design 108 cases and qualitative interviews to assess its acceptability The final clinical trial version of the Recovery For EC program was developed to provide patients with a tool for self-monitoring recovery outcomes and offer clinical healthcare professionals guidance for implementing precise and personalized rehabilitation management
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None