Exploration the Effect of Walking Program in Patients With Colorectal Cancer
Exploration the Effect of Individualized Home-based Walking Program on Muscle Strength and Fatigue in Patients With Colorectal Cancer Both During and After Treatment
1 other identifier
interventional
237
1 country
1
Brief Summary
The aims of this four-year study are to
- 1.explore the relationships between fatigue and muscle strength (i.e., upper limbs and lower legs)
- 2.comparison with the effects of 8-week, 12-week moderate intensity of walking program on muscle strength and fatigue.
- 3.develop a clinical guidelines of home-based walking program for patients with colorectal cancer receiving active treatment and survivors in Taiwan.
- 4.explore the relationships among the self-report fatigue intensity and metabolism.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable colorectal-cancer
Started Oct 2011
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2011
CompletedFirst Submitted
Initial submission to the registry
April 4, 2012
CompletedFirst Posted
Study publicly available on registry
May 10, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2013
CompletedOctober 15, 2014
October 1, 2014
1.3 years
April 4, 2012
October 13, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Exploration the Effect of Walking Program in Patients With Colorectal Cancer.
change of walking program on muscle strength and fatigue
five-year study
Study Arms (2)
walking group
EXPERIMENTALusual care
NO INTERVENTIONInterventions
Eligibility Criteria
You may qualify if:
- Patients with colorectal cancer in receiving active treatment or completed treatment within 5years.
- Patients in Different Stages.
- Aged above 18.
You may not qualify if:
- KPS\<60
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Taiwan University Hospital
Taipei, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Shiow-Ching Shun, PhD
National Taiwan University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 4, 2012
First Posted
May 10, 2012
Study Start
October 1, 2011
Primary Completion
February 1, 2013
Study Completion
February 1, 2013
Last Updated
October 15, 2014
Record last verified: 2014-10