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Exit Interview for Breast Cancer
Phase 2
Waitlist Available
Led By Mariana Chavez Mac Gregor, MD
Research Sponsored by M.D. Anderson Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion and average of 1 year.
Awards & highlights
Study Summary
This trial will help reduce the delay in chemotherapy initiation for breast cancer patients by providing them with individual support.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion and average of 1 year.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion and average of 1 year.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
General Self-Efficacy (GSE) Scale Questionnaires
Trial Design
2Treatment groups
Experimental Treatment
Group I: Group 2 (Control Group)Experimental Treatment2 Interventions
Participants will follow routine clinical care, where chemotherapy start date is determined by the provider and patient.
Group II: Group 1 (Investigational Group)Experimental Treatment2 Interventions
Participants will complete an in-depth patient needs checklist to identify patient-specific barriers that could lead to a delay with starting chemotherapy.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Exit Interview
2022
N/A
~20
Find a Location
Who is running the clinical trial?
M.D. Anderson Cancer CenterLead Sponsor
2,967 Previous Clinical Trials
1,804,802 Total Patients Enrolled
147 Trials studying Breast Cancer
63,286 Patients Enrolled for Breast Cancer
Mariana Chavez Mac Gregor, MDPrincipal InvestigatorM.D. Anderson Cancer Center
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Your doctor has recommended chemotherapy for you. This includes pregnant women in their 2nd or 3rd trimester.You can understand and communicate in English and/or Spanish.
Research Study Groups:
This trial has the following groups:- Group 1: Group 1 (Investigational Group)
- Group 2: Group 2 (Control Group)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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