Clinical trial Recruiting at 1 site Interventional

Making MDT meetings more effective and safer with Salutare One Referral software

Official title: Single Cohort Before and After Mixed-methods Prospective Study to Investigate the Impact of the Salutare One Referral Software on Patient Outcomes, Safety and Effectiveness of Multi-Disciplinary Team (MDT) Meetings

Run by Salutare Group Ltd. · NCT07104955 · Data updated 2026-11-12

This project will try the Salutare One Referral software with NHS MDT members and coordinators to see if it speeds up meetings and improves the information used for treating solid tumors and sarcoma.

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Quick facts

Study typeInterventional
SexAll
Enrollment40 (estimated)
SponsorSalutare Group Ltd.
Industry-sponsored
Locations1 site (London)
StatusRecruiting
StartedJuly 31, 2025
Main results expectedJune 19, 2026
Study endsJuly 19, 2026
Registry record updatedAugust 5, 2025
Trial IDNCT07104955 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are MDT panel members, MDT coordinators, and clinical staff who prepare or submit MDT referrals at the participating NHS site.

Probably not a fit

Patients whose care is managed outside MDT processes or at hospitals not using this software are unlikely to benefit directly from this project.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Multi-Disciplinary Team (MDT) meetings are central to planning complex cancer care but can be slowed by incomplete information, repeated discussions, and administrative burden. This before-and-after study will observe MDT workflow without the software, then with Salutare One Referral in routine meetings, and then again without it to measure changes. MDT members and coordinators will complete questionnaires about feasibility, usability, and safety while the study analyses pseudonymized patient data to identify effects on decision-making and timeliness. The study focuses on implementation effectiveness, safety signals, and practical feasibility in an NHS specialist setting.

Why it matters

Potential benefit: If successful, the software could enable faster, better-coordinated care and reduce delays in treatment planning for patients.

How similar studies have gone: Similar digital MDT and referral tools have shown small to moderate improvements in meeting efficiency in pilot implementations, but large-scale evidence of clinical or patient-outcome benefit is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* MDT meeting Panel Members, Coordinators and staff submitting MDT referrals will take part in this study.

Exclusion Criteria:

* MDT meeting Panel Members, Coordinators and staff submitting MDT referrals who are unwilling or unable to take part in the study.

Where it's running

  • Royal National Orthopaedic Hospital
    London, United Kingdom
    Recruiting

Study contacts

  • Principal investigator: Kevin Moore, MD — Salutare Limited
  • Study coordinator: Liba Stones, MA, MBA
  • Email: liba@dicro.co.uk
  • Phone: +447443940319

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.