Behaviour Change for Cancer Survivors Trial

ConditionsCancerExercise
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Toronto

About this trial

This study will be a two-arm RCT, to examine the effects of an entirely virtual, 6-month supervised PA program plus standard exercise counselling (PA+EC) versus a supervised PA plus motivationally-enhanced behavioral counselling (PA+BC) on moderate to vigorous physical activity (MVPA) in cancer survivors. A 6-month post intervention follow-up (T2) and 1-year post intervention follow-up (T3; 1-year follow-up from post-intervention) will take place after the intervention to address maintenance. The intervention is designed using evidence-based research in the fields of exercise oncology using effective clinical design and theoretical approaches, including behaviour change techniques, to gradually increase MVPA to at least 90 minutes per week in cancer survivors as per the exercise guidelines for cancer survivors.

Eligibility criteria

Qualifiers

≥18 years of age

Confirmed diagnosis of cancer of any type (Stages I to III; localized)

Have completed primary cancer treatment within 5 years

At least 12 weeks after surgery completion

Disqualifiers

A medical condition that prohibits PA (e.g., joint restriction or weight bearing precautions)

Uncontrolled comorbidities or cardiovascular contraindications that would increase risk associated with supervised and unsupervised exercise (e.g., cardiac contraindications, severe arthritis, recent fall within the last 6-12 months)

Presence of advanced cancer (i.e., Stage IV; metastatic)

Pregnancy

Trial design

Treatments tested in this trial

  • Behavioural Counselling
  • Exercise Counselling

Treatment groups

236 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Toronto

Lead sponsor

Toronto Rehabilitation Institute

Collaborator

University of British Columbia

Collaborator