NCT05884073

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

77
On Track

Trial Health Score

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

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
8mo left

Started Jan 2025

Typical duration for not_applicable

Geographic Reach
1 country

2 active sites

Status
recruiting

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

Study Progress67%
Jan 2025Dec 2026

First Submitted

Initial submission to the registry

May 5, 2023

Completed
27 days until next milestone

First Posted

Study publicly available on registry

June 1, 2023

Completed
1.6 years until next milestone

Study Start

First participant enrolled

January 2, 2025

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

February 13, 2025

Status Verified

February 1, 2025

Enrollment Period

2 years

First QC Date

May 5, 2023

Last Update Submit

February 11, 2025

Conditions

Keywords

oncology health professionalsburnoutexercisephysical activitynature-based walking

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

EXPERIMENTAL

12-week, supervised circuit-based resistance training program (2-3 times/week).

Behavioral: Circuit-based Resistance Training

Nature Walking

ACTIVE COMPARATOR

12-weeks self-paced walking in nature (2-3 times/week).

Behavioral: Nature-based Walking

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.

Circuit-based resistance exercise

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.

Nature Walking

Eligibility Criteria

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

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

Study Sites (2)

Physical Activity and Cancer (PAC) Lab

Halifax, Nova Scotia, B3H 2Y9, Canada

RECRUITING

Physical Activity and Cancer (PAC) Lab

Halifax, Nova Scotia, B3H 4R2, Canada

RECRUITING

MeSH Terms

Conditions

Caregiver BurdenCompassion FatigueBurnout, PsychologicalMotor Activity

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehaviorMental FatigueFatigueSigns and SymptomsPathological Conditions, Signs and SymptomsOccupational Stress

Central Study Contacts

Melanie Keats, PhD

CONTACT

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

Locations