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Clinical Trial ● Currently Recruiting Non-phase study NCT07135271

BeSpoke Decision Support for Patients With Newly Diagnosed Localised Prostate Cancer

BeSpoke Decision Support for Patients With Newly Diagnosed Localised Prostate Cancer — Recruiting • Non-phase study • Oncology • NCT07135271.

📅 29 Jul 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT07135271
Sponsor
University College, London
Start
2026-07-22
ClinicaliQ Trial Snapshot
  • BeSpoke Decision Support for Patients With Newly Diagnosed Localised Prostate Cancer — Recruiting • Non-phase study • Oncology • NCT07135271.
  • What is being tested: A personalised decision support intervention (BeSpoke) that provides tailored treatment counselling to help newly diagnosed prostate cancer patients make informed choices between active treatment options (surgery, radiotherapy, active surveillance).
  • Patient eligibility overview: Men with newly diagnosed localised prostate cancer who are eligible for multiple treatment modalities and capable of participating in the randomised intervention comparing standard care versus personalised decision support.
Use This Page For
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  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The goal of this randomised clinical trial is to assess whether personalised treatment counselling can improve the decision-making experience in patients with a new diagnosis of localised prostate cancer. The main question it aims to answer is: • Does the Bespoke Decision Support tool reduce decisional conflict in those choosing between treatment options for localised prostate cancer? Researchers will compare the addition of the Bespoke Decision Support tool to standard treatment counselling versus standard counselling alone. Patient participants will: * Receive standard counselling with or without access to the Bespoke…

Eligibility Snapshot
  • for Patient-Participants: 1. Newly diagnosed localised prostate cancer 2. Clinically suitable for at least two of the following treatment options: 1. active surveillance 2. focal therapy 3. radical prostatectomy 4. external beam radiotherapy 3. Willing and able to provide informed consent

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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