Can a quick GP visit improve cancer care? new study aims to find out
NCT ID NCT06589414
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether it's possible for people diagnosed with solid tumors to have a follow-up visit with their general practitioner within 15 days of learning their diagnosis. Researchers will track how many patients actually attend this visit and why some might not. The goal is to see if adding this step to the cancer care pathway is practical and helpful.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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171 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Jun 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years. 2. Patient with a solid tumour whatever the organ. 3. Patient treated in one of the participating centres as part of a system for announcing the diagnosis of a solid cancer. 4. Patient undergoing cancer treatment in one of the participating centres. 5. Patient with a registered general practitioner in the Occitanie region. 6. Patient affiliated to a French Social Security scheme. 7. Patient having signed informed consent prior to inclusion in the study and prior to any specific procedure for the study. Exclusion Criteria: 1. Patient already included in another clinical trial concerning a care pathway. 2. Patient deprived of liberty or under legal protection (curatorship and guardianship, safeguard of justice). 3. Pregnant or breast-feeding woman.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CH Auch
Auch, France
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CH Carcassonne
Carcassonne, 11000, France
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CHU Larrey
Toulouse, France
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CHU Rangueil
Toulouse, France
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Institut Universitaire du Cancer de Toulouse - Oncopole
Toulouse, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A single arm, open label, dose-escalation phase i and dose-expansion phase IIa clinical study to evaluate the feasibility, safety, and efficacy of allogeneic chimeric antigen receptor (CAR) Gamma-Delta t cells CAR001 in subjects with Relapsed/Refractory solid tumors
- Can an antidepressant calm Chemotherapy's nerve pain?
- A new imaging agent aims to make solid tumors visible on PET scans
- Can a radioactive antibody seek out and destroy Hard-to-Treat tumors?
- Can a platform trial match the right drug combo to each tumor?
- Can immune cell infusions help fight solid tumors?