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Health Economic Evaluation of an Adapted Physical Activity Program for Women With Breast Cancer (EMEAPA)

Primary Purpose

Breast Neoplasm

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
APA Program
Recommendations for physical activity
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Neoplasm focused on measuring Physical Activity, Exercise, Exercise Therapy, Breast Neoplasms, Medical costs, Healthcare Costs

Eligibility Criteria

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

Inclusion Criteria: women with breast cancer any type of breast cancer, all grades, all stages during treatment: surgery +/- chemotherapy +/- radiotherapy +/- hormone therapy Exclusion Criteria: World Health Organization (WHO) 4 Unstable angina Uncontrolled Atrial fibrillation Uncontrolled high blood pressure Recent myocardial infarction or myocarditis or pericarditis or thromboembolic disease (less than 3 weeks) Aortic stenosis or valve disease to operate Cardiac or respiratory failure, with dyspnea at rest Symptomatic anemia, thrombocytopenia Lytic or painful bone metastases, Severe osteoporosis Severe infectious syndrome, Surgery in the last 3 weeks Extreme fatigue, sharp pain, dizziness, disturbance of consciousness, severe undernutrition Contraindication to the practice of an adapted physical activity programme Currently involved or exclusion period of a interventional study or adapted Physical Activity program Patient with protective measures (guardianship, curators, and deprivation of liberty). Pregnancy or breastfeeding Patient with severe functional limitations

Sites / Locations

  • Marie-Eve Rougé-Bugat

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

APA program Group

Physical activity recommendation Group

Arm Description

patients treated and monitored for breast cancer under the APA programme

patients treated and monitored for breast cancer who have received recommendations for physical activity

Outcomes

Primary Outcome Measures

Comparison of physical activity programmes
Evaluation of the differential cost-utility ratio (cost / QALY), according to the perspective of the community over a 12-month period, of an adapted physical activity program (APA) in comparison to conventional care, including simple recommendations for physical activity for patients with breast cancer during the active phase of treatment.

Secondary Outcome Measures

Breast cancer-specific quality of life
Breast Cancer Specific Quality of Life Questionnaire (QLQ) (BR23-QLQ-C30) is a 52-item questionnaire. The choices range from 1 "not at all" to 4 "very much".
Clinical efficacy
Progression-free survival measured for non-metastatic (relapse-free survival) and metastatic (progression-free survival) patients
Efficacy on specific functions
BR23-QLQ-C30 questionnaire. Breast Cancer Specific Quality of Life Questionnaire (BR23-QLQ-C30) is a 52-item questionnaire. The choices range from 1 "not at all" to 4 "very much".
Society impact (interview)
Zarit-Burden Interview
Society impact
Number of hours of informal help for basic and instrumental activities of daily life
Patient satisfaction
Patient satisfaction questionnaire (EORTC-IN-PATSAT32) is a 32-item questionnaire. The choices range from 1 "bad" to 4 "excellent".
Programme compliance rate
Traced by the reservation system for adapted physical activity (APA) sessions
Rate of hospital care
Direct medical costs
Rate of difference in the effect of the programme
Socioeconomic determinants (changes in income, socio-professional category, level of education and family environment)
Rate of financial benefit of the programme
Annual and 5-year net financial benefit of the systematic implementation of an adapted physical activity (APA) program

Full Information

First Posted
June 13, 2023
Last Updated
July 17, 2023
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT05949983
Brief Title
Health Economic Evaluation of an Adapted Physical Activity Program for Women With Breast Cancer
Acronym
EMEAPA
Official Title
Health Economic Evaluation of an Adapted Physical Activity Program for Women With Breast Cancer During the Active Phase of Treatment: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

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
Adapted physical activity (APA) was recognized as a non-drug therapy by the French Health Authority (HAS) in 2011. Very few studies have examined the efficiency of APA programs during the active phase of treatment in cancer patients. The investigators assumed that non-drug therapy such as APA could improve the quality of life and reduces health costs. The main objective of this study is to assess the efficiency of a standardized APA program, as compared to conventional management including simple recommendations for the practice of physical activity in women in phase active breast cancer treatment.
Detailed Description
Scientific rationale: The incidence of breast cancer in women is on the rise again over the period 2010-2018. The overall cost of cancer treatment is 16.8 billion euros, including 3.6 billion for drugs alone. The treatments are more and more prolonged, the proportion of anticancer drugs continues to increase with 10% of the amount reimbursed for drugs delivered in pharmacies in 2017. Adapted physical activity (APA) was recognized as a non-drug therapy by the HAS in 2011. It reduces certain side effects of treatments, as well as certain symptoms linked to the catabolic activity of the disease such as: fat gain, loss of muscle mass, physical deconditioning, fatigue or pain. For breast cancer, a meta-analysis showed that APA following adjuvant therapy may have a beneficial effect on quality of life. The APA shows in particular for breast cancer, a reduction in all-cause mortality as well as specific mortality and a reduction in recurrence.The prescription of APA has been allowed since the 2016 health law but there is no coverage by the French national health insurance fund (CNAM) despite the benefits shown. APA is only accessible in a few centers in France that have chosen to offer it to patients, thus creating social inequalities in health. Very few studies have examined the efficiency of APA programs during the active phase of treatment. They related to cohorts of 60 to 165 patients and uses different methods. The investigators decided to set up a study that can measure the efficiency of the standardized APA programs offered to patients diagnosed with breast cancer, assuming that non-drug therapy such as APA would improve the quality of life while reducing health costs. Description of the procedures: The intervention consists of an initial consultation appointment with a medical check-up and physical tests, then inclusion in the standardized APA program for 6 months. The control group will be offered the same initial consultation appointment with medical check-up and physical tests and will receive recommendations for physical practice as well as a calendar of activities to be practiced independently for 6 months. Inclusion in the APA program will be offered one year after inclusion. Follow-up: The data will be collected at T0, T + 3 months, T + 6 months, T + 9 months and T + 12 months in both arms. There will be 1 year of data analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasm
Keywords
Physical Activity, Exercise, Exercise Therapy, Breast Neoplasms, Medical costs, Healthcare Costs

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
866 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
APA program Group
Arm Type
Experimental
Arm Description
patients treated and monitored for breast cancer under the APA programme
Arm Title
Physical activity recommendation Group
Arm Type
Active Comparator
Arm Description
patients treated and monitored for breast cancer who have received recommendations for physical activity
Intervention Type
Other
Intervention Name(s)
APA Program
Intervention Description
Patients treated and monitored for their breast cancer following the 6-month APA program.
Intervention Type
Other
Intervention Name(s)
Recommendations for physical activity
Intervention Description
Patients treated and monitored for their breast cancer who have received recommendations for physical activity as well as a 6-month activity schedule. To facilitate patient acceptance and participation in this study, patients who will be randomized to the control group will be offered to follow the APA program after one year of inclusion
Primary Outcome Measure Information:
Title
Comparison of physical activity programmes
Description
Evaluation of the differential cost-utility ratio (cost / QALY), according to the perspective of the community over a 12-month period, of an adapted physical activity program (APA) in comparison to conventional care, including simple recommendations for physical activity for patients with breast cancer during the active phase of treatment.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Breast cancer-specific quality of life
Description
Breast Cancer Specific Quality of Life Questionnaire (QLQ) (BR23-QLQ-C30) is a 52-item questionnaire. The choices range from 1 "not at all" to 4 "very much".
Time Frame
12 months
Title
Clinical efficacy
Description
Progression-free survival measured for non-metastatic (relapse-free survival) and metastatic (progression-free survival) patients
Time Frame
12 months
Title
Efficacy on specific functions
Description
BR23-QLQ-C30 questionnaire. Breast Cancer Specific Quality of Life Questionnaire (BR23-QLQ-C30) is a 52-item questionnaire. The choices range from 1 "not at all" to 4 "very much".
Time Frame
12 months
Title
Society impact (interview)
Description
Zarit-Burden Interview
Time Frame
12 months
Title
Society impact
Description
Number of hours of informal help for basic and instrumental activities of daily life
Time Frame
12 months
Title
Patient satisfaction
Description
Patient satisfaction questionnaire (EORTC-IN-PATSAT32) is a 32-item questionnaire. The choices range from 1 "bad" to 4 "excellent".
Time Frame
12 months
Title
Programme compliance rate
Description
Traced by the reservation system for adapted physical activity (APA) sessions
Time Frame
12 months
Title
Rate of hospital care
Description
Direct medical costs
Time Frame
12 months
Title
Rate of difference in the effect of the programme
Description
Socioeconomic determinants (changes in income, socio-professional category, level of education and family environment)
Time Frame
12 months
Title
Rate of financial benefit of the programme
Description
Annual and 5-year net financial benefit of the systematic implementation of an adapted physical activity (APA) program
Time Frame
5 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: women with breast cancer any type of breast cancer, all grades, all stages during treatment: surgery +/- chemotherapy +/- radiotherapy +/- hormone therapy Exclusion Criteria: World Health Organization (WHO) 4 Unstable angina Uncontrolled Atrial fibrillation Uncontrolled high blood pressure Recent myocardial infarction or myocarditis or pericarditis or thromboembolic disease (less than 3 weeks) Aortic stenosis or valve disease to operate Cardiac or respiratory failure, with dyspnea at rest Symptomatic anemia, thrombocytopenia Lytic or painful bone metastases, Severe osteoporosis Severe infectious syndrome, Surgery in the last 3 weeks Extreme fatigue, sharp pain, dizziness, disturbance of consciousness, severe undernutrition Contraindication to the practice of an adapted physical activity programme Currently involved or exclusion period of a interventional study or adapted Physical Activity program Patient with protective measures (guardianship, curators, and deprivation of liberty). Pregnancy or breastfeeding Patient with severe functional limitations
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie-Eve Rougé-Bugat, MD
Phone
5 61 80 01 23
Ext
+33
Email
marieeve.rouge-bugat@dumg-toulouse.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie-Eve Rougé-Bugat, MD
Organizational Affiliation
University Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Marie-Eve Rougé-Bugat
City
Toulouse
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie-Eve Rougé-Bugat, MD
Phone
561800123
Ext
+33
Email
marieeve.rouge-bugat@dumg-toulouse.fr
First Name & Middle Initial & Last Name & Degree
Marie-Eve Rougé Bugat

12. IPD Sharing Statement

Learn more about this trial

Health Economic Evaluation of an Adapted Physical Activity Program for Women With Breast Cancer

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