Clinical trial · Observational
Mobile Application to Collect PRO Data in NET Patients
NCT04324502CI-TRIAL-00048194unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Observational trial to assess the feasibility of monitoring patient reporting symptoms via mobile devices
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Neuroendocrine Neoplasms (Tumours) | Neuroendocrine Neoplasm | ONTOLOGY_EXACT | 0.85 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (1)
- label
- Neuroendocrine neoplasms (tumours)
- description
- Patients with a diagnosis of neuroendocrine neoplasm who are due to undergo one of the following treatments: chemotherapy, everolimus, sunitinib, somatostatin analogues, peptide receptor targeted therapy, embolization/ ablative therapies or surgery.
Primary outcomes (1)
- measure
- Reporting compliance
- timeFrame
- 4 years
- description
- The primary endpoint is patient reporting compliance, defined as the number of days with any patient report submitted during the course of treatment. This will be unique to each course of therapy since they have different durations of treatment.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically confirmed diagnosis of a NET * Planned treatment for NET * Able to give informed consent * Able to understand the language of the questionnaires * A minimum expected survival of 6 months * All performance status is acceptable * 18 years of age or over Exclusion Criteria: * Concurrent malignancies for which they are undergoing treatment * No smartphone / device * Any physical, psychological or comprehension problems that prevents completion of questionnaires.
References
Publications (0)
Data not yet available
No reference posted for this study.