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UW WELL-FIT Exercise Program for Cancer Patients

Not Applicable
Active, not recruiting
Conditions
Cancer
Interventions
Behavioral: Exercise
Registration Number
NCT02734394
Lead Sponsor
University of Waterloo
Brief Summary

The purpose of this project is to help to manage the many cancer treatment side effects through cardiovascular and resistance exercise, and education with the goal of using program outcomes to contribute to current research.

Detailed Description

This study is a single group pre-test post-test design.There are 4 optional measures that will be presented to participants from which they can choose to participate or not. These are presented with check boxes in the consent form. After completion of the University of Waterloo (UW) WELL-FIT program, participants will be given an option to continue with an exercise program; they will be offered the Graduate Program. Following consent of Graduate Program, repeated measures would be taken annually. At the time of consent, they will have the option to have their data used in research. At any point in their involvement of the exercise based programs, they can indicate "they no longer want to participate in the program or the data collection". Their medical care or participation in the UW WELL-FIT program will not be affected.

Procedures

1. UW WELL-FIT advertisement for Grand River Regional Cancer Centre

2. UW WELL-FIT brochure

3. Referral Form

4. Participants initial consultation and assessment

5. Obtain consent for UW WELL-FIT

6. Obtain Participant Information

7. Completion of FACIT-F survey

8. Metabolism \& Body Composition - Information sheet for optional measures

9. Physical Activity Survey- Godin Questionnaire

10. Provide 3-Day food diary and Nutritional Assessment

11. Fitness assessment, exercise programming and data entry:

1. Submaximal cardiovascular cycle ergometer or treadmill graded exercise test

2. Muscular strength using force transducer

3. Body composition:

* Height, weight and waist girth

* Bioelectrical Impedance Analysis (BIA)

* Dual Energy X-ray Absorption (Optional)

4. Range of motion using a goniometer

5. Blood sampling (Optional)

6. Design Individualized exercise program

12. UW WELL-FIT - Commencement of participant in 12 week exercise program (2 x 60 minute classes)

13. Post assessment (repeated pre-test assessments)

14. Pre and post data are entered into database

15. Summary and Feedback Report

16. Graduate Program: participant selects to attend UW WELL-FIT Graduate Program

17. Participants have annual reassessments in the Graduate Program

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • previously diagnosed with cancer and will currently be receiving some form of treatment (chemotherapy, radiation therapy or hormonal therapy)
Exclusion Criteria
  • Physical / health factors that prohibit exercise or lack of medical clearance from physician

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Cardiovascular and strength training exerciseExercise24 sessions (\~12 weeks) exercise
Primary Outcome Measures
NameTimeMethod
Maximal Exercise Test24 sessions (12 weeks)

Pre and post maximum workload using an electronic cycle ergometer in Watts

Percent Body Fat24 sessions (12 weeks)

Pre and Post percent body fat (units: %)

Upper and Lower Limb Strength24 sessions (12 weeks)

pre and post strength in upper and lower limb muscles using a linear differential variable transducer (LVDT) measured in Newton.meters

Body Mass Index24 sessions (12 weeks)

Pre and post body mass index (kg/m2)

Secondary Outcome Measures
NameTimeMethod
Glucose24 sessions (12 weeks)

measurement of blood glucose in mM

Lipids24 sessions (12 weeks)

measurement of total cholesterol, low density lipoprotein,high density lipoprotein ( millimole per liter (mM/L)

Trial Locations

Locations (1)

University of Waterloo

🇨🇦

Waterloo, Ontario, Canada

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