Exercise for Oncology Care Professionals
C4C+
The Cost of Caring: Examining the Role of Exercise in Mitigating Oncology Care Provider Burnout (C4C+)
1 other identifier
interventional
70
1 country
2
Brief Summary
The goal of this preference-based pilot study will be to assess the feasibility and acceptability, and impact of a 12-week exercise intervention on oncology care provider burnout. Participants self-select to participate into one of two exercise groups. Group assignment will be based on participant preference. Group 1: Supervised circuit-based resistance exercise Group 2: Nature-based walking
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2025
Typical duration for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 5, 2023
CompletedFirst Posted
Study publicly available on registry
June 1, 2023
CompletedStudy Start
First participant enrolled
January 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
February 13, 2025
February 1, 2025
2 years
May 5, 2023
February 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Feasibility - Participant Fidelity (Intervention Adherence)
Participant adherence to prescribed exercise intervention
Through study completion (about 2 years)
Feasibility - Safety
Adverse and serious adverse events
Through study completion (about 2 years)
Feasibility - Retention/Attrition
Percentage of participants who complete the 12-week intervention
Through study completion (about 2 years)
Feasibility - Attendance
Attendance is calculated as the percentage of exercise sessions completed by the total number of available exercise sessions over the 12-week intervention.
Through study completion (about 2 years)
Feasibility - Recruitment
Participant accrual as defined as the number of eligible participants who express an interest in participation divided by the number of participants who consent to participate.
Through study completion (about 2 years)
Feasibility - Participant Experience
Interviews with a diverse group of participants will be used to assess factors influencing participant selection of intervention type/setting, adherence to and satisfaction with the selected intervention.
Through study completion (about 2 years)
Secondary Outcomes (8)
Maslach Burnout Inventory (MBI) for Medical Personnel (MP)
Baseline, mid-program (6-weeks), and post intervention (12-weeks).
Physical Activity Behavior - Self-reported
Baseline, mid-program (6-weeks), and post intervention (12-weeks).
Resting heart rate
Pre to post intervention (12-week change)
Resting Blood Pressure
Pre to post intervention (12-week change)
Aerobic fitness
Pre to post intervention (12-week change)
- +3 more secondary outcomes
Study Arms (2)
Circuit-based resistance exercise
EXPERIMENTAL12-week, supervised circuit-based resistance training program (2-3 times/week).
Nature Walking
ACTIVE COMPARATOR12-weeks self-paced walking in nature (2-3 times/week).
Interventions
Participants will engage in a 12-week circuit-based resistance training program 2-3 times/week. Each supervised session will last about 30 minutes and will consist of 5 resistance exercises. Each exercise will be completed for 1 minute for a total of 5 minutes followed by a 1-minute rest. The circuit will then repeated 3 additional times (total of 4 circuits). All resistance sessions will be supervised by a certified fitness professionals.
Participants will be asked to engage in 30 minutes of self-paced walking in nature 2-3 days/week. Participants will be provided with a list of resources that direct them to walkable nature/green spaces close to their home or workplace.
Eligibility Criteria
You may qualify if:
- years of age or older;
- Able to speak/write in English;
- Must be providing formal care to cancer patients in a clinical setting within the Halifax Municipality;
- Actively practicing within the Nova Scotia Cancer Care Program; and
- Able and willing to engage in low-to-moderate intensity physical activity.
You may not qualify if:
- Exceeding Canadian physical activity guidelines of 150-minutes of moderate-to-vigorous physical activity per week; and
- Any health condition that would preclude safe participation in a new exercise program.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Melanie Keatslead
Study Sites (2)
Physical Activity and Cancer (PAC) Lab
Halifax, Nova Scotia, B3H 2Y9, Canada
Physical Activity and Cancer (PAC) Lab
Halifax, Nova Scotia, B3H 4R2, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 5, 2023
First Posted
June 1, 2023
Study Start
January 2, 2025
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
February 13, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share