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RJBC-APP and Breast Cancer Treatment Compliance

Primary Purpose

Breast Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
The RJBC-APP
Routine post-surgical follow-up
Sponsored by
Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Cancer

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Females aged 18-70 Eastern Cooperative Oncology Group Performance Status Score 0-2 Breast cancer by pathology Adjuvant therapy by multidisciplinary team Written informed consent form Exclusion Criteria: Distant metastases at diagnosis Unable to use a smartphone

Sites / Locations

  • Xiaosong Chen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

The RJBC-APP group

The Control group

Arm Description

Participants randomized to the RJBC-APP group should register on the RJBC-APP, through which they can receive treatment reminders, matters needing attention as well as science knowledge and communicate with the medical staff.

Participants randomized to the Control group have no access to the RJBC-APP and post-surgical follow-up can only be conducted in outpatient clinic.

Outcomes

Primary Outcome Measures

Rate of compliance with adjuvant therapy
Compliance is defined as completing the adjuvant therapy recommended by multidisciplinary team in terms of the type, dosage, date and course, and non-compliance is considered in the presence of any of the following cases: 1) the patient refuses to accept the recommended treatments, 2) the actual treatments are different from those recommended, 3) the patient dose not complete the full course of treatments, 4) the patient starts the treatment 7 days or more later than the established date, 5) the patient does not follow the recommended dose and intensity.
Overall Survival (OS)
OS is calculated from the date of surgery to the date of death.

Secondary Outcome Measures

Rate of compliance with adjuvant therapy
Compliance is defined as completing the adjuvant therapy recommended by multidisciplinary team in terms of the type, dosage, date and course, and non-compliance is considered in the presence of any of the following cases: 1) the patient refuses to accept the recommended treatments, 2) the actual treatments are different from those recommended, 3) the patient dose not complete the full course of treatments, 4) the patient starts the treatment 7 days or more later than the established date, 5) the patient does not follow the recommended dose and intensity.
Quality of Life (QoL) Scale
The QoL Scale is evaluated by the European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30, version 3.0). The questionnaire is composed of 30 items among which items 1-28 are divided into 4 levels (scored as 1-4 respectively, higher scores mean a worse outcome) and items 29-30 are divided into 7 grades (scored as 1-7 respectively, higher scores mean a better score). The items are further divided into 15 domains. The standard score (0-100) is calculated from raw score of each domain and higher scores mean a better outcome.
Cancer-related symptoms scores
Cancer-related symptoms are evaluated by the MD Anderson Symptom Inventory (MDASI). The questionnaire is composed of 19 items among which items 1-13 are degree of 13 common symptoms and items 14-19 are degrees of the impact on daily life (scored as 1-10 respectively, higher scores mean a better score). The total score (0-190) is calculated by sum of each item and higher scores mean a worse outcome.
Disease-free Survival (DFS)
DFS is calculated from the date of surgery to the first date of the following events: local recurrence, regional recurrence, distant metastasis, contralateral breast cancer, secondary primary malignancy and death.

Full Information

First Posted
May 2, 2023
Last Updated
June 26, 2023
Sponsor
Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT05921331
Brief Title
RJBC-APP and Breast Cancer Treatment Compliance
Official Title
Mobile Medical Application on Adjuvant Therapy Compliance and Quality of Life in Patients With Early Breast Cancer: a Multicentric, Open-labeled, Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 1, 2023 (Anticipated)
Primary Completion Date
July 1, 2025 (Anticipated)
Study Completion Date
August 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Jiao Tong University School of Medicine

4. Oversight

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

5. Study Description

Brief Summary
The goal of this multicentric randomized controlled clinical trial is to test the role of mobile medical application (APP) on adjuvant therapy compliance and quality of life (QoL) in patients with early breast cancer. Participants assigned to the Ruijin Breast Cancer APP (RJBC-APP) group can receive treatment reminders, matters needing attention as well as science knowledge and they can communicate with the medical staff during adjuvant treatments while follow-up can only be conducted in outpatient clinic for those in the Control group.
Detailed Description
Adjuvant treatments has significantly improved the prognosis of early breast cancer patients. However, previous studies suggested the existence of noncompliance to adjuvant therapies, which might cause detriments to disease outcomes. The goal of this multicentric randomized controlled clinical trial is to test the role of mobile medical application (APP) on adjuvant therapy compliance and quality of life (QoL) in patients with early breast cancer. Patients diagnosed with invasive breast cancers after surgery will be randomly assigned to the Ruijin Breast Cancer APP (RJBC-APP) group or the Control group. Those in the RJBC-APP group can receive treatment reminders, matters needing attention as well as science knowledge and they can communicate with the medical staff during adjuvant treatments while follow-up can only be conducted in outpatient clinic for those in the Control group. The primary endpoint is the rate of adjuvant therapy compliance at 12 months after randomization. Secondary endpoints consist of compliance rates at 3, 6, 24 months after randomization, QoL and cancer-related symptoms scores at 3, 6, 12, 24 months, disease-free survival (DFS) and overall survival (OS) at 60 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
The RJBC-APP group
Arm Type
Experimental
Arm Description
Participants randomized to the RJBC-APP group should register on the RJBC-APP, through which they can receive treatment reminders, matters needing attention as well as science knowledge and communicate with the medical staff.
Arm Title
The Control group
Arm Type
Active Comparator
Arm Description
Participants randomized to the Control group have no access to the RJBC-APP and post-surgical follow-up can only be conducted in outpatient clinic.
Intervention Type
Device
Intervention Name(s)
The RJBC-APP
Other Intervention Name(s)
RJBC Full-Course Management APP
Intervention Description
The RJBC-APP consists of the following features: 1. Login, logout, setting, and modification of personal information. 2. Full-course management included registering for information on the surgical treatment, viewing the results of the multidisciplinary team (MDT) discussion, generating the treatment process according to the MDT discussion, receiving the reminder of the treatment, confirming the completion of the treatment, filling in the follow-up information, and consulting a specialist nurse. 3. Questionnaire and feedback.
Intervention Type
Other
Intervention Name(s)
Routine post-surgical follow-up
Intervention Description
The routine post-surgical follow-up is conducted in the outpatient clinic.
Primary Outcome Measure Information:
Title
Rate of compliance with adjuvant therapy
Description
Compliance is defined as completing the adjuvant therapy recommended by multidisciplinary team in terms of the type, dosage, date and course, and non-compliance is considered in the presence of any of the following cases: 1) the patient refuses to accept the recommended treatments, 2) the actual treatments are different from those recommended, 3) the patient dose not complete the full course of treatments, 4) the patient starts the treatment 7 days or more later than the established date, 5) the patient does not follow the recommended dose and intensity.
Time Frame
12 months after adjuvant therapy
Title
Overall Survival (OS)
Description
OS is calculated from the date of surgery to the date of death.
Time Frame
60 months after adjuvant therapy
Secondary Outcome Measure Information:
Title
Rate of compliance with adjuvant therapy
Description
Compliance is defined as completing the adjuvant therapy recommended by multidisciplinary team in terms of the type, dosage, date and course, and non-compliance is considered in the presence of any of the following cases: 1) the patient refuses to accept the recommended treatments, 2) the actual treatments are different from those recommended, 3) the patient dose not complete the full course of treatments, 4) the patient starts the treatment 7 days or more later than the established date, 5) the patient does not follow the recommended dose and intensity.
Time Frame
3、6 and 24 months after adjuvant therapy
Title
Quality of Life (QoL) Scale
Description
The QoL Scale is evaluated by the European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30, version 3.0). The questionnaire is composed of 30 items among which items 1-28 are divided into 4 levels (scored as 1-4 respectively, higher scores mean a worse outcome) and items 29-30 are divided into 7 grades (scored as 1-7 respectively, higher scores mean a better score). The items are further divided into 15 domains. The standard score (0-100) is calculated from raw score of each domain and higher scores mean a better outcome.
Time Frame
3、6、12 and 24 months after adjuvant therapy
Title
Cancer-related symptoms scores
Description
Cancer-related symptoms are evaluated by the MD Anderson Symptom Inventory (MDASI). The questionnaire is composed of 19 items among which items 1-13 are degree of 13 common symptoms and items 14-19 are degrees of the impact on daily life (scored as 1-10 respectively, higher scores mean a better score). The total score (0-190) is calculated by sum of each item and higher scores mean a worse outcome.
Time Frame
3、6、12 and 24 months after adjuvant therapy
Title
Disease-free Survival (DFS)
Description
DFS is calculated from the date of surgery to the first date of the following events: local recurrence, regional recurrence, distant metastasis, contralateral breast cancer, secondary primary malignancy and death.
Time Frame
60 months after adjuvant therapy

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Females aged 18-70 Eastern Cooperative Oncology Group Performance Status Score 0-2 Breast cancer by pathology Adjuvant therapy by multidisciplinary team Written informed consent form Exclusion Criteria: Distant metastases at diagnosis Unable to use a smartphone
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaosong Chen, Professor
Phone
021-64370045
Email
chenxiaosong0156@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Siji Zhu, MD
Phone
021-64370045
Email
zsj_mu@yeah.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaosong Chen, Professor
Organizational Affiliation
Xiaosong Chen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xiaosong Chen
City
Shanghai
State/Province
Please Select
ZIP/Postal Code
200025
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaosong Chen, Professor
Phone
021-64370045
Email
chenxiaosong0156@hotmail.com
First Name & Middle Initial & Last Name & Degree
Siji Zhu, MD
Phone
021-64370045
Email
zsj_mu@yeah.net
First Name & Middle Initial & Last Name & Degree
Xiaosong Chen, Professor
First Name & Middle Initial & Last Name & Degree
Siji Zhu, MD
First Name & Middle Initial & Last Name & Degree
Nan Zhang

12. IPD Sharing Statement

Plan to Share IPD
No

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RJBC-APP and Breast Cancer Treatment Compliance

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