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UW WELL-FIT Exercise Program for Cancer Patients

U

University of Waterloo

Status

Active, not recruiting

Conditions

Cancer

Treatments

Behavioral: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT02734394
ORE18987-A

Details and patient eligibility

About

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.

Full 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

UW WELL-FIT advertisement for Grand River Regional Cancer Centre UW WELL-FIT brochure Referral Form Participants initial consultation and assessment Obtain consent for UW WELL-FIT Obtain Participant Information Completion of FACIT-F survey Metabolism & Body Composition - Information sheet for optional measures Physical Activity Survey- Godin Questionnaire Provide 3-Day food diary and Nutritional Assessment

Fitness assessment, exercise programming and data entry:

Submaximal cardiovascular cycle ergometer or treadmill graded exercise test Muscular strength using force transducer

Body composition:

Height, weight and waist girth Bioelectrical Impedance Analysis (BIA) Dual Energy X-ray Absorption (Optional) Range of motion using a goniometer Blood sampling (Optional) Design Individualized exercise program UW WELL-FIT - Commencement of participant in 12 week exercise program (2 x 60 minute classes) Post assessment (repeated pre-test assessments) Pre and post data are entered into database Summary and Feedback Report Graduate Program: participant selects to attend UW WELL-FIT Graduate Program Participants have annual reassessments in the Graduate Program

Enrollment

200 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Cardiovascular and strength training exercise
Experimental group
Description:
24 sessions (~12 weeks) exercise
Treatment:
Behavioral: Exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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