Actively Recruiting
Exercise Intervention to Improve Quality of Life in Patients With Colorectal Cancer
Led by National Taiwan University Hospital Hsin-Chu Branch · Updated on 2024-03-19
106
Participants Needed
1
Research Sites
305 weeks
Total Duration
On this page
Sponsors
N
National Taiwan University Hospital Hsin-Chu Branch
Lead Sponsor
N
National Taipei University of Nursing and Health Sciences
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Exercise Intervention to Improve Quality of Life in Patients With Colorectal Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
A. Inclusion criteria
- Above the age of 20, with colorectal cancer pathological stage in situ, I, II, and III.
- Coherent, with no mental abnormalities.
- Able to read Mandarin or communicate in Mandarin and Taiwanese to complete the questionnaire.
- Provided informed consent.
- No physical disabilities.
B. Exclusion criteria
- Acute inflammation of the limbs and joints.
- Previous abdominal surgery within 3 months.
- Symptomatic cardiovascular events.
- Long-term anti-depressant drug use.
- Unilateral restrictions of the upper or lower limbs.
- History of medium- or high-intensity exercise for more than half a year.
- Having colostoma or ileostoma.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
NTU Hsin-Chu Hospital
Hsinchu, Taiwan, 300
Actively Recruiting
Research Team
Z
Zih-Yun Deng, BSN
CONTACT
H
Hui-Mei Chen, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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