Clinical trial · Observational
Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.
- 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)
In the present study, we have trained 10 patients in subcutaneous self-administration of Velcade. After their training, patients will alternately receive their treatment in the hospital and at home by self-administration. In keeping with common practice, a nurse contacts the patients by telephone before 9.00 am on the day of treatment to ensure that the patient is physically "fit" to receive the medication and to discuss any side effects. To highlight the advantages and disadvantages of the changed treatment practice from the perspectives of both patients and healthcare professionals, data is collected from two consecutive semi-structured interviews with n = 10 patients and n = 1 focus group interview of the healthcare professionals involved. Moreover, time registration of medication administration both at the hospital and in the patients' home is done. The qualitative data will be analyzed via the method of condensation and continual quantitative data will form the basis of a cost-benefit analysis.
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 |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Bortezomib | Drug | Bortezomib | ALIAS |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Patients experience of self-administration of Velcade
- timeFrame
- Through study completion, from 01. dec. 2019 until 01. jun. 2022
- description
- Qualitative interviews with all 10 included patients
Secondary outcomes (3)
- measure
- Organizational perspective
- timeFrame
- Through study completion, from 01. dec. 2019 until 01. jun. 2022
- description
- Patients and health professionals (including pharmacy staff) registration of time spend on treatment on all 10 included patients.
- measure
- Health care perspective
- timeFrame
- Through study completion, from 01. dec. 2019 until 01. jun. 2022
- description
- Focus group interview with healthcare professionals involved in the treatment.
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion criteria * Patients must have Multiple Myeloma * Patients (or their relatives) must be deemed physically and cognitively suitable and willing for self-administration of subcutaneous Velcade * Patients must be able to understand and speak Danish * Patients must have received a minimum of 1 treatment cycle in the outpatient clinic Exclusion criteria * Lack of willingness to participate in scheduled interviews * Patients who are cognitively affected * Must not be receiving trial treatment
References
Publications (0)
Data not yet available