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Cluster randomised controlled trial of the impact of the Australian Cancer Trials online website

Cluster randomised controlled trial of the impact of the Australian Cancer Trials online website on the proportion of patients with whom the possibility of participation in any clinical trial is discussed with their medical oncologist.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12608000273381
Acronym
ACT Online
Enrollment
30
Registered
2008-05-29
Start date
2008-12-01
Completion date
Unknown
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

This a randomised controlled trial of a website called Australian Cancer Trials Online. This website provides information about cancer clinical trials in Australia. The trial will look at the effect of the website on clinial trial recruitment and doctor patient communication about cancer clinical trials.

Interventions

The intervention is the Australian Cancer Trials Online website. This will be a website that provides up to date information about the cancer clinical trials currently recruiting patients in Australia. It will contain two decision support tools (a question prompt list and decision aid) and consumer support information which will help consumers make a decision whether to participate in a clinical trial and increase their knowledge and understanding of cancer clinical trials. Medical oncologists a

The intervention is the Australian Cancer Trials Online website. This will be a website that provides up to date information about the cancer clinical trials currently recruiting patients in Australia. It will contain two decision support tools (a question prompt list and decision aid) and consumer support information which will help consumers make a decision whether to participate in a clinical trial and increase their knowledge and understanding of cancer clinical trials. Medical oncologists and patients in the intervention arm will have access to the website. The consultation between each of the participating medical oncologists and their patients will be audio-taped. Each patient will have their consultation audio-taped once. The duration of the intervention is for 6 months.

Sponsors

Dr Rachel Dear
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

Patients invited to participate in the study must be: 1) Patients starting treatment for the first time. For example: new patients, patients not initially suitable for chemotherapy but are currently suitable due to symptomatic disease or improved performance status. 2) Patients in whom a treatment change is anticipated. For example: in the adjuvant setting a patient with early breast cancer finishing adjuvant chemotherapy and about to start adjuvant endocrine therapy and in the metastatic setting patients with progressive disease needing to change chemotherapy or all lines of chemotherapy utilised. 3) Patients with email and internet access. 4) Patients due to see their medical oncologist in 2 weeks time over a period of 4 to 8 weeks (longer may be necessary).

Exclusion criteria

Medical oncologists working outside NSW and Victoria and medical oncologists who do not have email and internet access. Patients who do not have email and internet access, who are already participating in a clinical trial and do not have command of English.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026