Ignite Creation Date:
2025-12-25 @ 5:02 AM
Ignite Modification Date:
2025-12-26 @ 4:03 AM
Study NCT ID:
NCT05224518
Status:
RECRUITING
Last Update Posted:
2024-03-19
First Post:
2021-12-12
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Exercise Intervention to Improve Quality of Life in Patients With Colorectal Cancer
Sponsor:
National Taiwan University Hospital Hsin-Chu Branch
Organization:
Study Overview
Official Title:
National Taiwan University Hospital Hsin-Chu Branch.
Status:
RECRUITING
Status Verified Date:
2024-03
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:
None
Brief Summary:
The purpose of this study was to explore the 12-week effectiveness of home exercise intervention for colorectal cancer patients in improving fatigue, sleep, muscle endurance, and quality of life.
A. Explore the effect of "12-week home exercise intervention" in improving the fatigue of colorectal cancer patients.
B. Explore the effect of "12-week home exercise intervention" in improving the sleep quality of patients with colorectal cancer.
C. Explore the effect of "12-week home exercise intervention" in improving the muscle endurance of patients with colorectal cancer.
D. Explore the effect of "12-week home exercise intervention" in improving the quality of life of colorectal cancer patients.
A. Explore the effect of "12-week home exercise intervention" in improving the fatigue of colorectal cancer patients.
B. Explore the effect of "12-week home exercise intervention" in improving the sleep quality of patients with colorectal cancer.
C. Explore the effect of "12-week home exercise intervention" in improving the muscle endurance of patients with colorectal cancer.
D. Explore the effect of "12-week home exercise intervention" in improving the quality of life of colorectal cancer patients.
Detailed Description:
The study was conducted at the colon and rectal outpatient departments. A randomized controlled trial design was adopted. The participants were divided into an interventional group and a conventional therapy control group based on block randomization in a 1:1 ratio. Data were collected when patients returned to the clinic.
Study Oversight
Has Oversight DMC:
False
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?: