NCT06960291

Brief Summary

EXCEL will provide online and, where feasible, in-person exercise programs to individuals living with and beyond cancer (ILWBC). Research has shown that targeted programs that include tailored exercise prescriptions are more successful in helping individuals with chronic disease to incorporate physical activity and exercise into their daily routines. While ILWBC are advised by healthcare professionals (HCPs) to engage in exercise, there is a lack of cancer-specific exercise programs and cancer-trained exercise specialists in Canada, outside of the research setting. Considering the negative impact cancer and its treatments have on fitness and physical activity levels, community-based efforts towards improving access, uptake and maintenance of exercise programming are needed. This study will evaluate the benefits of a community-based or online EXCEL exercise program for people living with and beyond cancer across Canada, using a streamlined intake process compared to the original EXCEL Study (HREBA.CC-20-0098, NCT04478851). This 8 to 12-week program (intervention) will be delivered in-person or over virtual platform. It includes twice weekly supervised exercise classes.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
740

participants targeted

Target at P75+ for not_applicable cancer

Timeline
7mo left

Started Mar 2025

Geographic Reach
1 country

5 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress67%
Mar 2025Nov 2026

Study Start

First participant enrolled

March 11, 2025

Completed
24 days until next milestone

First Submitted

Initial submission to the registry

April 4, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 7, 2025

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2026

Last Updated

October 7, 2025

Status Verified

March 1, 2025

Enrollment Period

1.6 years

First QC Date

April 4, 2025

Last Update Submit

October 2, 2025

Conditions

Keywords

Exercise oncologyExercisePhysical activitycommunity programonline exercisecancer survivorindividual living with and beyond cancerquality of life

Outcome Measures

Primary Outcomes (1)

  • Physical Activity Level

    The Modified Godin Leisure Time Exercise Questionnaire is used to determine subjective levels of physical activity in each participant.

    Baseline to one year

Secondary Outcomes (11)

  • Cancer related symptoms

    Baseline to one year

  • Cost-effectiveness

    Baseline to one year

  • Fatigue

    Baseline to one year

  • Quality of life

    Baseline to one year

  • Body Composition

    Baseline to 12-weeks

  • +6 more secondary outcomes

Study Arms (1)

Intervention

EXPERIMENTAL

All participants will be involved in group exercise classes, twice a week for 8-12 weeks.

Behavioral: Group Exercise Classes

Interventions

Participants will take part in a combination of aerobic, resistance, balance, and flexibility exercises delivered in a circuit-type class setting, twice weekly for a 8-12-week period (duration of intervention depends on scheduling logistics for the coordinating hubs and their spokes sites). The exercise sessions will be conducted in groups with a ratio of up to 15 participants per instructor. The program follows exercise progression principles (i.e., frequency, intensity, time, type, overload and progression) over the 8-12-weeks, with tailoring of any exercise to meet individual participant needs as required, in order to promote fitness and wellness benefits.

Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • have or had a diagnosis of cancer;
  • be 18 years or older;
  • be able to participate in low-intensity levels of activity, at minimum;
  • be pretreatment, or receiving active cancer treatment (i.e., surgery, systemic therapy and radiation therapy), have received cancer treatment within the past 3 years, or if beyond 3 years since treatment completion, have a referral from their healthcare team indicating they have side effects from cancer treatment or the cancer itself, that could be improved or managed with exercise;
  • be able to provide informed written consent in English or French

You may not qualify if:

  • does not or did not have a cancer diagnosis
  • is under the age of 18
  • is unable to participate in mild exercise, at minimum
  • is not pretreatment, or receiving active cancer treatment (i.e., surgery, systemic therapy and radiation therapy), has not received cancer treatment within the past 3 years, or if beyond 3 years since treatment completion, doesn't have side effects from cancer treatment or the cancer itself, that could be improved or managed with exercise
  • unable to read/write in English
  • for online programs, does not have internet or computer access

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (5)

University of Calgary

Calgary, Alberta, T2N1N4, Canada

RECRUITING

University of British Columbia

Vancouver, British Columbia, V6T 1Z7, Canada

RECRUITING

Nova Scotia Health Authority

Halifax, Nova Scotia, B3H 4R2, Canada

RECRUITING

University of Toronto

Toronto, Ontario, M5S 1A1, Canada

RECRUITING

Centre hospitalier de l'Université de Montréal

Montreal, Quebec, H2X 0A9, Canada

RECRUITING

MeSH Terms

Conditions

NeoplasmsProstatic NeoplasmsBreast NeoplasmsColonic NeoplasmsLung NeoplasmsMotor Activity

Condition Hierarchy (Ancestors)

Genital Neoplasms, MaleUrogenital NeoplasmsNeoplasms by SiteGenital Diseases, MaleGenital DiseasesUrogenital DiseasesProstatic DiseasesMale Urogenital DiseasesBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesColorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRespiratory Tract NeoplasmsThoracic NeoplasmsLung DiseasesRespiratory Tract DiseasesBehavior

Study Officials

  • Nicole Culos-Reed, PhD

    University of Calgary

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Julianna Dreger, PhD

CONTACT

Georgia Kaluznick

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Model Details: Hybrid effectiveness-implementation study
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 4, 2025

First Posted

May 7, 2025

Study Start

March 11, 2025

Primary Completion (Estimated)

October 30, 2026

Study Completion (Estimated)

November 30, 2026

Last Updated

October 7, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

No plan at this time to share IPD outside of the research team.

Locations