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ANZ 1301 (DOMINO): Exploring decision making about neoadjuvant chemotherapy for operable breast cancer.

ANZ 1301 (DOMINO): Women who have had a diagnosis of invasive breast cancer in the last 5 years and were offered or discussed neoadjuvant chemotherapy as a treatment option, will participate in a telephone questionnaire to identify factors influencing their decisions about neoadjuvant chemotherapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12613000658718
Acronym
DOMINO
Enrollment
20
Registered
2013-06-17
Start date
2013-07-29
Completion date
2013-08-26
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The study aims to identify relevant issues and information needs of women who have considered or have had neoadjuvant chemotherapy treatment within the last five years for initially operable cancer, and incorporate them into a prospective questionnaire and decision aid for women diagnosed with operable breast cancer considering neoadjuvant chemotherapy. Who is it for? You may be eligible to join this study if you are aged over 18 years, have had a diagnosis of invasive breast cancer in the last 5 years, have been offered or have discussed neoadjuvant chemotherapy as a treatment option and have completed a surgical intervention for breast cancer. Trial details Participants in this study will be interviewed once over the phone to identify the issues faced and their prevalence and impact on decision making, and the level of distress associated with treatment for women who have considered or have had neoadjuvant chemotherapy treatment within the last five years for initially operable breast cancer. The findings will be incorporated into a prospective questionnaire and subsequent decision aid for women considering neoadjuvant chemotherapy for operable breast cancer.

Interventions

Telephone questionnaire. Each participant will do the questionnaire once. The questionnaire will take approximately 30 minutes. The first few questions are to check that the interview is right for the participant. The next questions are for general information on age, location (postcode only) and some general information about health insurance and where the participant was treated (public or private hospital). The rest of the questions will ask about: * Breast cancer diagnosis * What things t

Telephone questionnaire. Each participant will do the questionnaire once. The questionnaire will take approximately 30 minutes. The first few questions are to check that the interview is right for the participant. The next questions are for general information on age, location (postcode only) and some general information about health insurance and where the participant was treated (public or private hospital). The rest of the questions will ask about: * Breast cancer diagnosis * What things the particpant thought about, or might think about, to help them decide whether or not to have chemotherapy before breast cancer surgery * What treatments the participant had for their breast cancer * What were their worries and concerns while they were having treatment for breast cancer * What information women should have, before deciding whether or not to have chemotherapy before breast cancer surgery. Some questions will have different answers to choose from and others also allow for comments to be made. Ten to twenty interviews will be conducted to identify the majority of relevant issues. The aim is for issue saturation, where no major new issues are raised in three consecutive interviews.

Sponsors

Australia and New Zealand Breast Cancer Trials Group
Lead SponsorOther Collaborative groups

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1) Participants must be female, >=18 years 2) Participants have had a diagnosis of invasive breast cancer in the last 5 years 3) Participants have been offered, or have discussed, neoadjuvant chemotherapy as a treatment option 4) Participants have completed surgical intervention for breast cancer 5) Participants are capable of giving informed consent

Exclusion criteria

1) Hearing or other impairment that would preclude a phone interview 2) Insufficient English language skills for participation

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026