NCT07009886 · M.D. Anderson Cancer Center
Development of an Educational Patient Decision Aid (Treatments in Advanced Cancer - Decision Aid, TA-DA) to Promote Shared Decision Making for Third-line or Beyond Palliative Systemic Therapy
What this study is about
To develop an educational patient decision aid for advanced cancer patients to prepare them to have conversations with their clinicians about treatment options (Treatments in Advanced cancer - Decision Aid, TA-DA).
View original scientific description
To develop an educational patient decision aid for advanced cancer patients to prepare them to have conversations with their clinicians about treatment options (Treatments in Advanced cancer - Decision Aid, TA-DA).
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Clinicians (Part I/II/III): MD Anderson medical oncologists and APPs who provide care to patients with advanced cancer
- Patients (Part I/II/III): Age 18 or over
- Diagnosis of advanced cancer (i.e., metastatic, relapsed, and/or incurable disease as defined by the treating oncologist) who has received at least 2 lines of palliative systemic therapy\
- Patient-rated ECOG performance status of 1-3 for Part I/II and 2-3 for Part III
- Able to make treatment decisions based on the clinical judgement of the oncology team
- English speaking
- patient has started, is receiving, and/or has completed second-line palliative systemic therapy or beyond
- Caregivers (Part I/II/III):
- Age 18 or older
- Currently a primary caregiver to a patient who satisfies the patient eligibility criteria listed above
- For the study purposes, a primary caregiver is defined as:
- someone who provides physical, emotional, decisional and/or logistical assistance to the patient regularly (e.g. daily, weekly);
- can be a family member, friend, or other individual in a close relationship with the patient;
- must be identified by the patient and self-identify as the primary person providing caregiving support to the patient
- Able to provide informed consent and participate in the study
- English speaking
Exclusion criteria
- Any patient who meets any of the following criteria will be excluded from participation in this study:
- (Part I/II/III): Diagnosis of cognitive impairment or dementia requiring a surrogate decision maker as determined by the clinical team
- (Part III only): Participants in Part I and II
Where
- Houston, Texas
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Feb 19, 2026 · Source of record for eligibility and locations