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Community Based Exercise Program for Well Cancer Survivors (CanWell)

This study has been completed.
Sponsor:
Collaborator:
McMaster University
Information provided by (Responsible Party):
Oren Cheifetz, Hamilton Health Sciences Corporation
ClinicalTrials.gov Identifier:
NCT00798200
First received: November 25, 2008
Last updated: March 2, 2016
Last verified: March 2016

November 25, 2008
March 2, 2016
March 2009
December 2015   (final data collection date for primary outcome measure)
  • Endurance measure (STEEP treadmill test) [ Time Frame: Within one week before initiating the exercise program ] [ Designated as safety issue: No ]
  • Endurance measure (STEEP treadmill test) [ Time Frame: Administered at 6 weeks of the exercise program ] [ Designated as safety issue: No ]
  • Endurance measure (STEEP treadmill test) [ Time Frame: Administered at 12 weeks (end of) the exercise program ] [ Designated as safety issue: No ]
Endurance measure (STEEP treadmill test) [ Time Frame: Pre and Post 12 week exercise program ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00798200 on ClinicalTrials.gov Archive Site
Not Provided
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Community Based Exercise Program for Well Cancer Survivors
CanWell: YMCA Based Exercise Program for Well Cancer Survivors
This project will create a community based exercise program for well cancer survivors. The goal is that the YMCA will gain the competence to work with this unique population in a safe and productive manner.
All well, adult, cancer survivors are eligible to participate.
Interventional
Phase 1
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Supportive Care
Cancer
Other: Exercise program
All exercise programs will include endurance and strength exercises.
Exercise
All participants will take part in a supervised, structured, exercise program
Intervention: Other: Exercise program

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
200
January 2016
December 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • All well cancer survivors who are medically stable.

Exclusion Criteria:

  • Children are not eligible for this project.
Both
16 Years and older   (Child, Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00798200
WorkForceOntario 001
No
Not Provided
Not Provided
Oren Cheifetz, Hamilton Health Sciences Corporation
Hamilton Health Sciences Corporation
McMaster University
Not Provided
McMaster University
March 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP