General Resources

Trial Management in the UK and Ireland

A Cross-sectional Survey of Workforce, Training and Professional Recognition Trial Managers (TMs) are central to the successful delivery of academic clinical trials. Their responsibilities have expanded to include project management, regulatory compliance, site engagement, recruitment oversight, and stakeholder communication. Despite this, concerns remain that increasing expectations are not matched by appropriate authority, resources, or professional […]

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Trial Forge Guidance 4: a guideline for reporting the results of randomised Studies Within A Trial (SWATs)

Trial Forge Guidance 4 helps trial teams to develop  SWAT reporting guideline will aid authors, reviewers, and journal editors to produce and review clear, structured reports of randomised SWATs, whilst also adhering to the CONSORT guideline. An editable version of the checklist, to accompany publication submission, can be downloaded via the Download Resource Link button

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Principles for handling end-of-participation events in trials (PeRSEVERE)

The right to stop taking part, or change how to take part PeRSEVERE has its own website: https://persevereprinciples.org/ All guidelines, policies and laws about clinical trials and other research with human participants are clear that, before taking part in research, individuals must voluntarily give informed consent, and that they can withdraw that consent at any

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Protocols and resources for priority recruitment and retention SWATs (PRESS)

The ‘Protocol and resource development for prioritised recruitment and retention strategies’ (PRESS) project aimed to develop these protocols, and resources, to assist and encourage trial teams to evaluate the recruitment and retention strategies in their trials, especially those that we have prioritised for evaluation. We have developed protocols, guidance and other resources for four recruitment

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