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.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Salutare Group Ltd. Industry-sponsored |
| Locations | 1 site (London) |
| Status | Recruiting |
| Started | July 31, 2025 |
| Main results expected | June 19, 2026 |
| Study ends | July 19, 2026 |
| Registry record updated | August 5, 2025 |
| Trial ID | NCT07104955 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
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
MIGHTY: CAR T cells targeting B7-H3 for pediatric, teen, and young adult sarcoma
This Phase 1 trial tests autologous hBRCA84D CAR T cells in kids, teens, and young adults (1–24) with relapsed or refractory RMS, ES, or DSRCT to see if the therapy is feasible and safe.
-
Lifileucel (Tumor-infiltrating lymphocytes) for advanced soft tissue sarcoma
This study tests lifileucel, a cell therapy made from a patient’s own tumor cells, in adults with unresectable or metastatic soft tissue sarcoma who have had prior treatments to see if it helps shrink tumors and improve outcomes.
-
Domatinostat with Sirolimus for relapsed or refractory sarcoma and osteosarcoma
This study tests whether the cancer drugs domatinostat and sirolimus together can help adolescents and adults whose sarcoma or osteosarcoma has come back or stopped responding to standard therapy.
-
Steroid-Sparing Plan with Olanzapine and Palonosetron to Prevent Nausea in High-Dose Cisplatin
This phase II trial tests a steroid-sparing regimen using olanzapine and palonosetron to prevent chemotherapy-induced nausea and vomiting in patients getting high-dose cisplatin.
-
Clonal Hematopoiesis Effects with Chemo and Radiation in Solid Cancers
This study tests whether clonal hematopoiesis affects outcomes for adults with solid cancers who are receiving chemotherapy or radiation.
-
Dietary Supplements and Cancer Patients: Use, Tolerance, and Interactions
This study looks at how many cancer patients take dietary supplements, how they tolerate them, and whether these supplements interact with cancer treatments.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.