Clinical trial · Interventional
Evaluation of the Impact of a Follow-up Phone Call Nurse Device in the Care of Patients With Chemotherapy Treatment
Evaluation of the Impact of a Follow-up Phone Call Nurse Device in the Care of Patients With Chemotherapy Treatment, in Their Quality of Life and Medico-economic Analysis of This Follow-up Program Device
NCT02619045CI-TRIAL-00031894EVAL'COACHcompletedN/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)
This study evaluate the Impact of a Follow-up Phone Call Nurse Device in the Care of Patients With Chemotherapy Treatment, in their Quality of Life and Medico-economic Analysis of this Follow-up Program Device.
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 |
|---|---|---|---|
| Solid Tumors | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Telephone follow-up nursing device | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Solid tumors
- description
- Patients with solid tumor starting a intra venous chemotherapy with 21 days cycles.
- interventionNames
- Other: Telephone follow-up nursing device
Primary outcomes (1)
- measure
- Efficacy : Proportion of patients for which there was a modification in their care through the nurse device
- timeFrame
- 24 months
Secondary outcomes (4)
- measure
- Safety according to the classification of the CTCAE (Common for Toxicity Criteria for Adverse effects) V4.0
- timeFrame
- 24 months
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patient with a solid tumor. 2. Patient starting a first cycle of chemotherapy (+ - targeted therapy). 3. Patient starting intravenous chemotherapy including 21-day cycles. 4. Patient ≥18 years old. 5. Patient affiliated to a social security system in France. 6. Patient who signed the informed consent before study inclusion and before any study specific procedure. Exclusion Criteria: 1. Patient already included in another interventional biomedical research. 2. Patient who began intravenous chemotherapy. 3. Patient who must receive an oral chemotherapy. 4. Patient who must be treated with a weekly chemotherapy or with concomitant radiotherapy. 5. Patient unreachable by phone. 6. Patient with no caregiver who can answer the phone in his place. 7. Pregnant or breastfeeding women. 8. Any psychological condition, family, geographic or social not to comply with medical monitoring and / or procedures in the study protocol. 9. Patient protected by law.
References
Publications (0)
Data not yet available
No reference posted for this study.