Clinical trial · Interventional
Digital Symptom Tracking, Patient Engagement and Quality of Life in GI Oncology Clinic Patients
Feasibility Study of Digital Symptom Tracking, Patient Engagement and Quality of Life in Patients Seen in GI Oncology Clinic
NCT03459352CI-TRIAL-00046823completedN/AClinicalTrials.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)
A pilot study of an ePRO system in cancer patients receiving systemic therapies.
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 |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ePRO | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- ePRO
- description
- There is no therapeutic intervention. Patients will use ePRO system to report systems. We will describe use in patients to determine compliance in reporting symptoms.
- interventionNames
- Other: ePRO
Primary outcomes (1)
- measure
- Subject participation
- timeFrame
- 12 months
- description
- total number of subjects that participate in the use of a web-based system
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Individuals (men and women) aged 18 years or older 2. History cancer with no limitation on prior lines of therapy in the metastatic setting 3. ECOG performance status of 0-2 4. Estimated life expectancy of at least 12 months 5. Access to smartphone, tablet or computer with capability to utilize symptom-tracking application 6. Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures 7. Willing and able to comply with all study procedures Exclusion Criteria: 1. Concurrent disease or condition that interferes with participation or safety 2. Non-English speaking, as the application is developed in the English language 3. Children will not be included in the study. The pattern of disease and symptoms are different in children than in an adult population. The web-based tool was designed based on the symptom experience of adults with cancer.
References
Publications (0)
Data not yet available
No reference posted for this study.