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Implementing Exercise Into Clinical Practice in Breast Cancer Care (NEXT-BRCA)

Primary Purpose

Breast Cancer

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exercise
Self-Management
Booster Sessions
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring exercise, physical activity, self-management

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • community-dwelling
  • English-speaking women
  • over 18 years of age
  • currently undergoing adjuvant or neoadjuvant chemotherapy for Stage 1-3 breast cancer
  • cleared by their oncologist to participate in moderate intensity aerobic exercise

Exclusion Criteria:

  • self-report any chronic condition, cognitive impairment, or injury that would prevent them from participating independently in moderate intensity exercise

Sites / Locations

  • Juravinski Cancer Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Institution-Based Exercise and Self-Management (EXSM)

Institution-Based Self-management only (SM)

Usual care

Arm Description

Eight session of supervised exercise within the cancer institution plus 8 self-management modules focusing on goal setting and action planning for safe and effective exercise strategies (this is based on our team's successful pilot intervention). Four booster sessions will be provided to this group.

Eight SM sessions for safe and effective exercise strategies will be provided to this group (described above). Four booster sessions will be provided to this group.

Participants in this group will receive care as normally provided by their treating oncologist. This can be heterogeneous between different physicians and centres, but usually includes oncologists encouraging their patients to 'stay active'

Outcomes

Primary Outcome Measures

Change in baseline physical activity level
To be assessed using the Godin Leisure Time Exercise Questionnaire (total score 0-no maximum; higher scores indicating higher levels of physical activity) and activity tracker (Fitbit) data (demonstrating steps/day and total time of moderate levels of physical activity; higher scores indicate higher levels of activity).

Secondary Outcome Measures

Change in baseline quality of life
Measured using the Functional Assessment of Cancer Therapy-Breast (measure of quality of life in breast cancer survivors; scale range 0-144; higher scores indicate higher levels of quality of life).
Change in level of exercise knowledge
Measured using the Theory of Planned Behaviour (TPB) based questionnaire (scale range 7-56; higher scores indicate higher levels of exercise knowledge).
Change in baseline perception of health status
Measured using the EQ-5D-3L a measure of health status (has two systems; a 3 level scale assessing five dimensions of health and a visual analogue scale from 0-10; higher scores indicate higher perceptions of health status)
Change in baseline aerobic capacity
Measured using the Six-minute walk test (6MWT) (a performance based measure that assesses total distance walked in six minutes, higher scores indicate higher levels of aerobic capacity)
Change in baseline levels of lower extremity strength
Measured using a manual muscle dynamometer (Movements assessed will be isometric hip and knee flexion/extension and ankle plantar flexion/dorsiflexion; higher scores indicate higher levels of lower extremity strength).
Change in patient engagement in health services
Measured using the Patient Health Engagement Scale (assesses five domains related to the experiences and preferences of patients for their engagement with their health care treatment; score range from 5-35; higher scores indicate higher levels of patient engagement in health services).
Change in baseline levels of resting BP
To measure change in cardiovascular outcomes; Measured with sphygmamometer
Change in baseline resting heart rate
To measure change in cardiovascular outcomes; Measured with pulsed oximeter

Full Information

First Posted
September 5, 2019
Last Updated
March 8, 2023
Sponsor
Hamilton Health Sciences Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT04109274
Brief Title
Implementing Exercise Into Clinical Practice in Breast Cancer Care
Acronym
NEXT-BRCA
Official Title
Evaluation of a Novel Strategy to Implement Exercise Evidence Into Clinical Practice in Breast Cancer Care: The NEXT-BRCA Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 3, 2019 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamilton Health Sciences Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
BACKGROUND: One in eight women will develop breast cancer in their lifetime. With improved screening and treatment techniques, more women are surviving breast cancer. However, women live with physical and emotional side effects secondary to treatment for years after cancer treatments have ended. Exercise can help to manage these side effects, however, less than 30% of this population takes part in regular exercise. The objective of this trial is to determine the feasibility and effectiveness of a novel exercise and education program for women with breast cancer during chemotherapy. METHODS: Participants in this study include women with a diagnosis of stage 1 - 3 breast cancer undergoing chemotherapy. Women will be divided into three groups. The first group will include 8 sessions of exercise and self-management education during their chemotherapy treatment. The second group will receive self-management education only, and the third group will receive usual care. Outcomes will be compared between groups at baseline, post-intervention, and at 6- and 12- month follow up. Outcomes to be assessed include exercise level, functional mobility, muscle strength, quality of life, health status, and use of health care services. EXPECTED OUTCOMES: Women with breast cancer are among the least active segment of the Canadian population. It is well known that inactivity can lead to physical and psychological side effects, cancer recurrence, and an increase in comorbid conditions. This proposed project addresses a long-standing need to help women with breast cancer become and stay more active by implementing a novel exercise and education program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
exercise, physical activity, self-management

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
85 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Institution-Based Exercise and Self-Management (EXSM)
Arm Type
Experimental
Arm Description
Eight session of supervised exercise within the cancer institution plus 8 self-management modules focusing on goal setting and action planning for safe and effective exercise strategies (this is based on our team's successful pilot intervention). Four booster sessions will be provided to this group.
Arm Title
Institution-Based Self-management only (SM)
Arm Type
Experimental
Arm Description
Eight SM sessions for safe and effective exercise strategies will be provided to this group (described above). Four booster sessions will be provided to this group.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Participants in this group will receive care as normally provided by their treating oncologist. This can be heterogeneous between different physicians and centres, but usually includes oncologists encouraging their patients to 'stay active'
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Other Intervention Name(s)
Physical Activity; self-management
Intervention Description
Exercise component: Aerobic exercise, using recumbent bikes, delivered within the cancer institution. Participants will take part in up to 30-minutes of moderate intensity (50-70% HRmax or 4-6/10 on Rate of Perceived Exertion scale)6 exercise for eight sessions during chemotherapy. An exercise specialist with experience in cancer rehabilitation will supervise the exercise component.
Intervention Type
Behavioral
Intervention Name(s)
Self-Management
Intervention Description
Eight SM modules will be delivered to participants. They will be viewed on an iPad prior to or after the exercise component. The goal of these modules is to aid participants in developing physical activity goals and action plans to continue with between sessions, with an overarching goal of helping them reach exercise guidelines for cancer survivors and the Canadian Physical Activity Guidelines
Intervention Type
Behavioral
Intervention Name(s)
Booster Sessions
Intervention Description
Four booster sessions will be provided to participants in this group. These will occur at 2, 4, 6, and 8 months post intervention completion. An assessor trained in behavioural counselling will provide booster sessions by phone and will discuss the individuals physical and emotional condition, current exercise level, accomplishment of previously set goals and action plans, and perceived barriers to participation in exercise. The assessor will use facilitation strategies to aid participants in devising strategies to overcome barriers and set realistic goals and action plans.
Primary Outcome Measure Information:
Title
Change in baseline physical activity level
Description
To be assessed using the Godin Leisure Time Exercise Questionnaire (total score 0-no maximum; higher scores indicating higher levels of physical activity) and activity tracker (Fitbit) data (demonstrating steps/day and total time of moderate levels of physical activity; higher scores indicate higher levels of activity).
Time Frame
16-weeks, 6-months, 12-months
Secondary Outcome Measure Information:
Title
Change in baseline quality of life
Description
Measured using the Functional Assessment of Cancer Therapy-Breast (measure of quality of life in breast cancer survivors; scale range 0-144; higher scores indicate higher levels of quality of life).
Time Frame
16-weeks, 6-months, 12-months
Title
Change in level of exercise knowledge
Description
Measured using the Theory of Planned Behaviour (TPB) based questionnaire (scale range 7-56; higher scores indicate higher levels of exercise knowledge).
Time Frame
16-weeks, 6-months, 12-months
Title
Change in baseline perception of health status
Description
Measured using the EQ-5D-3L a measure of health status (has two systems; a 3 level scale assessing five dimensions of health and a visual analogue scale from 0-10; higher scores indicate higher perceptions of health status)
Time Frame
16-weeks, 6-months, 12-months
Title
Change in baseline aerobic capacity
Description
Measured using the Six-minute walk test (6MWT) (a performance based measure that assesses total distance walked in six minutes, higher scores indicate higher levels of aerobic capacity)
Time Frame
16-weeks, 6-months, 12-months
Title
Change in baseline levels of lower extremity strength
Description
Measured using a manual muscle dynamometer (Movements assessed will be isometric hip and knee flexion/extension and ankle plantar flexion/dorsiflexion; higher scores indicate higher levels of lower extremity strength).
Time Frame
16-weeks, 6-months, 12-months
Title
Change in patient engagement in health services
Description
Measured using the Patient Health Engagement Scale (assesses five domains related to the experiences and preferences of patients for their engagement with their health care treatment; score range from 5-35; higher scores indicate higher levels of patient engagement in health services).
Time Frame
16-weeks, 6-months, 12-months
Title
Change in baseline levels of resting BP
Description
To measure change in cardiovascular outcomes; Measured with sphygmamometer
Time Frame
16-weeks, 6-months, 12-months
Title
Change in baseline resting heart rate
Description
To measure change in cardiovascular outcomes; Measured with pulsed oximeter
Time Frame
16-weeks, 6-months, 12-months
Other Pre-specified Outcome Measures:
Title
Recruitment rate
Description
Percentage of eligible patients actually enrolled in the study.
Time Frame
At recruitment completion (approximately 1 year).
Title
Retention rate
Description
Percentage of enrolled patients who complete the intervention.
Time Frame
At intervention completion (Approximately 1.3 years).
Title
Drop out rate throughout study
Description
Percentage of participants who drop out from study at any time.
Time Frame
At study completion (2 years)
Title
Representativeness of study sample
Description
Descriptive characteristics of study samples (in regard to characteristics such as age, stage of cancer, fitness level, socio-economic status, etc.)
Time Frame
At recruitment completion (approximately 1 year).
Title
Adherence rate to intervention
Description
Percentage of total intervention sessions attended.
Time Frame
At intervention completion (Approximately 1.3 years)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: community-dwelling English-speaking women over 18 years of age currently undergoing adjuvant or neoadjuvant chemotherapy for Stage 1-3 breast cancer cleared by their oncologist to participate in moderate intensity aerobic exercise Exclusion Criteria: self-report any chronic condition, cognitive impairment, or injury that would prevent them from participating independently in moderate intensity exercise
Facility Information:
Facility Name
Juravinski Cancer Centre
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8V 5C2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33178447
Citation
Smith-Turchyn J, Mukherjee S, Richardson J, Ball E, Bordeleau L, Neil-Sztramko S, Levine O, Thabane L, Sathiyapalan A, Sabiston C. Evaluation of a novel strategy to implement exercise evidence into clinical practice in breast cancer care: protocol for the NEXT-BRCA randomised controlled trial. BMJ Open Sport Exerc Med. 2020 Oct 7;6(1):e000922. doi: 10.1136/bmjsem-2020-000922. eCollection 2020.
Results Reference
derived

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Implementing Exercise Into Clinical Practice in Breast Cancer Care

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