search
Back to results

Role of Individualized Intervention(s) in Hormone-Receptor Positive Early-stage Breast Cancer (MyCHOICE)

Primary Purpose

Breast Cancer, Premenopausal Breast Cancer, Hormone Receptor Positive Tumor

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Individualized interventions
Sponsored by
University of Saskatchewan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Premenopausal breast cancer, Individualized interventions, Exercise, Combination hormone therapy, Massage therapy, Yoga, Acupuncture, Treatment tolerance, Treatment adherence, Adverse effects, Quality of life

Eligibility Criteria

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

Inclusion Criteria:

• Premenopausal women with histologically-proven, completely resected, hormone receptor-positive (defined as ER≥10% and/or PgR≥10%) stage 1, 2, and 3 invasive breast cancer who are treated with combination of anti-estrogen therapy (LHRH agonist and an aromatase inhibitor or tamoxifen)

Exclusion Criteria:

  • Post-menopausal women
  • Women who are on single agent endocrine therapy

Sites / Locations

  • Allan Blair Cancer Center
  • Saskatoon Cancer Center

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Individualized interventions

Arm Description

Exercise, Yoga, massage therapy, acupuncture, and others

Outcomes

Primary Outcome Measures

Functional Assessment of Cancer Therapy - Breast Symptom Index (FACT-B)
For global assessment of quality of life of women with breast cancer

Secondary Outcome Measures

Functional Assessment of Cancer Therapy - Endocrine System (FACT-ES)
For the assessment of quality of life of women with breast cancer on endocrine therapy
Functional Assessment of Cancer Therapy - (FACT)-Cognitive
For the assessment of self-reported cognitive function
Treatment discontinuation rate
Rate of combination of endocrine treatment at 3 year.

Full Information

First Posted
October 24, 2017
Last Updated
May 16, 2022
Sponsor
University of Saskatchewan
search

1. Study Identification

Unique Protocol Identification Number
NCT03407768
Brief Title
Role of Individualized Intervention(s) in Hormone-Receptor Positive Early-stage Breast Cancer
Acronym
MyCHOICE
Official Title
Role of Individualized Intervention(s) on Quality of Life and Adherence to Adjuvant Endocrine Therapy in Premenopausal Women With Early-Stage Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Saskatchewan

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
Although combination endocrine therapy has been associated with significant reduction in risk of recurrence in younger women with hormone receptor positive breast cancer, it has been associated with more adverse effects and decline in quality of life (QOL). Various behavioral and complementary interventions can be effective in reducing treatment-related side effects. The study aims to evaluate if individually-tailored behavioral and complementary interventions could improve treatment tolerance and adherence in women with early stage breast cancer. This benefit will be assessed primarily by change in QOL and secondarily by adherence to adjuvant endocrine treatment.
Detailed Description
Recent evidence suggest that ovarian suppression in combination with exemestane compared with tamoxifen alone has been associated with significant reduction in risk of breast cancer recurrence in premenopausal women with high risk estrogen or progesterone receptor positive breast cancer. However, combination therapy has been associated with more adverse effects, poor treatment adherence, and decline in quality of life (QOL). Various behavioral and complementary interventions such as exercise, yoga, acupuncture, and massage therapy can be effective to reduce treatment-related side effects and thereby to improve QOL. Nevertheless, there is a paucity of evidence about effect of individualized behavioral and complementary interventions in younger women who are treated with combination endocrine therapy. The study aims to evaluate if younger women with early stage breast cancer treated with combination endocrine therapy could benefit from individualized behavioral and complementary intervention (s) during their treatment. This benefit will be assessed primarily by change in QoL and cognitive function from the baseline measurement and secondarily by adherence to adjuvant endocrine treatment. Furthermore, the study will explore correlation between selection of intervention(s) and various socio-demographic and clinical factors. Forty premenopausal women with early stage breast cancer treated with combination endocrine therapy will be recruited over a two year period in Saskatchewan with a median follow up period of about two years. All participants will be provided a list of interventions that alone or in combination could be helpful to improve treatment tolerance to hormonal therapy. A participant will be able to select one or more intervention based on her preferences. The QOL and cognitive function will be assessed every three months using Functional Assessment of Cancer Therapy - Breast Symptom Index (FACT-B), FACT - Endocrine System (FACT-ES), and FACT-Cognitive Function scales. Treatment adherence will be monitored monthly basis. Individually-tailored behavioral and complementary interventions could promote self-management and empower the women with early stage breast cancer to manage treatment related side effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Premenopausal Breast Cancer, Hormone Receptor Positive Tumor
Keywords
Premenopausal breast cancer, Individualized interventions, Exercise, Combination hormone therapy, Massage therapy, Yoga, Acupuncture, Treatment tolerance, Treatment adherence, Adverse effects, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Individualized interventions
Arm Type
Other
Arm Description
Exercise, Yoga, massage therapy, acupuncture, and others
Intervention Type
Behavioral
Intervention Name(s)
Individualized interventions
Intervention Description
A participant will be able to select one or more (or no intervention) based on her preferences. Individualized exercise program Yoga and mindfulness Massage therapy Acupuncture Others: Women who are not interested in any above intervention but like to explore other interventions will be offered material pertinent to their choice of complimentary techniques.
Primary Outcome Measure Information:
Title
Functional Assessment of Cancer Therapy - Breast Symptom Index (FACT-B)
Description
For global assessment of quality of life of women with breast cancer
Time Frame
Up to three years from the time of enrolment
Secondary Outcome Measure Information:
Title
Functional Assessment of Cancer Therapy - Endocrine System (FACT-ES)
Description
For the assessment of quality of life of women with breast cancer on endocrine therapy
Time Frame
Up to three years from the time of enrolment
Title
Functional Assessment of Cancer Therapy - (FACT)-Cognitive
Description
For the assessment of self-reported cognitive function
Time Frame
Up to three years from time of enrolment
Title
Treatment discontinuation rate
Description
Rate of combination of endocrine treatment at 3 year.
Time Frame
Up to three years from the time of enrolment

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • Premenopausal women with histologically-proven, completely resected, hormone receptor-positive (defined as ER≥10% and/or PgR≥10%) stage 1, 2, and 3 invasive breast cancer who are treated with combination of anti-estrogen therapy (LHRH agonist and an aromatase inhibitor or tamoxifen) Exclusion Criteria: Post-menopausal women Women who are on single agent endocrine therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shahid Ahmed, MD, PhD
Organizational Affiliation
University of Saskatchewan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Allan Blair Cancer Center
City
Regina
State/Province
Saskatchewan
Country
Canada
Facility Name
Saskatoon Cancer Center
City
Saskatoon
State/Province
Saskatchewan
ZIP/Postal Code
S7N4H4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
If requested in future after meeting all the regulatory requirement data will be shared.

Learn more about this trial

Role of Individualized Intervention(s) in Hormone-Receptor Positive Early-stage Breast Cancer

We'll reach out to this number within 24 hrs