2026 ACTA Trial of the Year Awards

2026 ACTA Trial of the Year Award

Nominator details

Please enter your personal details so that the ACTA team can contact you, if required, to confirm any of the details provided.

Name
Name
First Name
Last Name

Awards category

I have read the award guidelines and believe this trial is eligible to be considered for (please tick all that apply)
I wish to nominate a:
ACTA member network or group that designed and led the trial.

Maximum file size: 134.22MB

ACTA Trial of the Year Award

If you are submitting a nomination for this award, please ensure all required information is provided to allow your application to be fully assessed.

Do you wish to nominate this trial for the Trial of the Year Award?
Please confirm that the trial meets the following eligibility criteria
Did this trial involve any commercial or industry collaboration?
Peer Summary

Please provide a brief summary (max 600 words) describing the trial and why it warrants recognition as the ACTA Trial of the Year. Please address each of the judging criteria below:

  1. The trial addressed a critical gap in the evidence or a significant innovation in healthcare delivery
  2. The quality of the research design, conduct and alanysis were outstanding
  3. There is a high likelihood that findings from the trial will significaltly impact clinical practice and policy and improve outcomes for patiends or healthcare delivery.

Maximum file size: 134.22MB

Plain English summary

ACTA STInG Excellence in Trial Statistics Award

If you are submitting a nomination for this award, please ensure all required information is provided to allow your application to be fully assessed.

Do you wish to nominate this trial for the ACTA STInG Excellence in Trial Statistics Award?
Please confirm that the primary results of this trial were published (online or in print) in 2025.
Please confirm that the that the statistical analysis plan is publicly available.
Statistical methods summary

Please provide a brief summary (600 words max) describing the statisticall design and alaysis of this trial and why it warrants consideration for the ACTA STInG Excellence in Trial Statistics award. Please address each of the judging criteria below:

  1. The statistical aspects of trial design and planning (sample size, randomisation, analytical methods_ were of high quality, appropriate for the research question(s), and documented in a publically accessible statistical procedures
  2. The stastical analyses were executed as planned and, where not, deviations were transparent, of quality, and executed well following good stastistical procedures/practices.
  3. The reporting and interpretation of the statistical aspects of the trial were appropriate, transparent, and supporting by results from pre-specified analyses and/or well-defended departures from planned procedures following good statistical procedures/pratice.

Please also include an overview of timelines (including dates of recruitment commencement and completion, dates of protocol versions and updates, dates of the statistical analysis plan including all versions and updates together with a changelog, dates of interim analyses (if relevant), date of database lock, and date of submission of the manuscript). In the case of multiple statistical analysis plans (e.g., publication, open repository, supplemental material), it must be indicated which plan should be considered as the final plan for evaluation by the Panel.

Supplemental materials

Please attach the final version of the supplemental materials listed below.

  1. Trial Protocol (for platform trials, please include the core protocol and any relevant domain specific appendix)
  2. Statistical Analysis Plan
  3. A timeline describing the date of the registration of the trial in trial registry, date first protocol approved, date first patient, date statistical analysis plan finalised and publicly available, date last patient recruited, date last patient last follow up, date of data lock, date analysis conducted, date of publication,

Maximum file size: 134.22MB

ACTA Consumer Involvement Award

If you are submitting a nomination for this award, please ensure all required information is provided to allow your application to be fully assessed.

Do you wish to nominate this trial for the ACTA Consumer Involvement Award?

Consumer involvement value

Describe the value to the study of consumer involvement in this clinical trial’s activities and why it warrants consideration for the ACTA Consumer Involvement Award (max 600 words). Examples may include experiential knowledge, which is often subjective or qualitative. Consider the criteria below:

  1. Consumers were significantly involved in protocol development or design activities
  2. Consumer involvement provided valuable and exceptional guidance to the proposed conduct of the trial

Maximum file size: 134.22MB

Plain English summary

Please provide a brief summary (400 words max) describing the benefit of consumer involvement in the trial, including, where appropriate, the consumer’s background and motivation for involvement. Plain English summaries should be suitable for publication on the ACTA website and in the general media.

ACTA HEAT Excellence in Trial based Health Economics Award

If you are submitting a nomination for this award, please ensure all required information is provided to allow your application to be fully assessed.

Do you wish to nominate this trial for the ACTA HEAT Excellence in Trial Based Health Economics Award?
Please confirm that the health economic analysis of this trial was published (online or in print) in 2025
Peer summary

Please describe the health economic analysis and why it warrants consideration for the ACTA-HEAT Excellence in Trial Based Health Economics Award (600 words maximum). Consider the criteria below:

  1. The health economics aspects of trial design and planning (e.g. collection and valuation of healthcare use data, patient-reported outcomes) were of high quality, and appropriate for the research question(s)
  2. The health economics analyses were executed as planned (e.g. as stated in the Health Economics Analysis Plan (HEAP) and, where not, deviations were transparent, of high quality, and well executed following best practices
  3. The reporting and interpretation of the health economic analyses and sensitivity analyses were appropriate, transparent, and supported by results
  4. The health economics analyses make a significant contribution to trials methodology, or health and social policy, or health impact.

Maximum file size: 134.22MB

Plain English summary

Please provide a plain English summary (400 words max) describing the health economic analysis and how the results are likely to impact patients and/or the delivery of healthcare. Plain English summaries should be suitable for publication on the ACTA website and in the general media.

Maximum file size: 134.22MB

ACTA Clinical Quality Registy Award

If you are submitting a nomination for this award, please ensure all required information is provided to allow your application to be fully assessed.

Do you wish to nominate this trial for the ACTA Clinical Quality Registry Award
ACTA Member Registry
ACTA Member Registry
Peer summary

Please provide a peer summary (600 words max) describing the registry and why it warrants consideration for the ACTA Clinical Quality Registry Award. Consider the criteria below:

  1. The governance of the registry: including demonstration of exceptional clinical and technical leadership, effective operational arrangements, the software and management systems in place, compliance with legislation and standards including participant identity controls and quality assurance processes
  2. Data quality: including the scope, scale and interoperability of the data, collection in alignment with core outcome sets and/or METEOR metadata standards (where defined), data linkage capacity and effective data analysis
  3. Impact: including reporting quality, engagement with relevant stakeholders and end-users of the data; relevant publications and the impact on health outcomes or services (annual reports may be attached as supporting evidence)

Consumer involvement: inclusion of consumer representatives and/or advisory committees and the collection of PROMs and/or PREMs (where appropriate)

Plain English summary

Please provide a plain English summary (400 words max) describing the registry and how the results have, or are likely to, impact patients and/or the delivery of healthcare. Plain English summaries should be suitable for publication on the ACTA website and in the general media.

Maximum file size: 134.22MB

ACTA TRIPSIG Excellence in Implementation Science Award

Please complete each section of this nomination form.

Do you wish to nominate this trial for the ACTA TRIPSIG Excellence in Implementation Science Award
Please confirm that the primary results of this trial were published (online or in print) in 2025.
Implementation science methods summary

Please provide a brief summary describing the implementation science design and analysis of this trial and why it warrants consideration for the ACTA TRIP SIG Excellence in Trial Implementation Science Award. In addition, please address each of the judging criteria:

  • The implementation science components of trial design and planning (e.g. theories, models, frameworks, strategy or intervention, outcomes, analytical methods) were of high quality, appropriate for the research question(s), and documented in a publicly accessible location.
  • The implementation analyses were executed as planned or – where not, deviations were transparent, of high quality, and executed well.
  • The reporting and interpretation of the implementation science components of the trial were appropriate and transparent

Maximum file size: 134.22MB

You are now ready to submit your nomination. Please ensure that all relevant documents have been uploaded to this submission and that you have filled in all the relevant areas for your nominated awards.

Please contact awards@acta.au should you have any questions.