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Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.

Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05163405
Enrollment
10
Registered
2021-12-20
Start date
2019-12-01
Completion date
2022-06-01
Last updated
2025-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Myeloma

Brief summary

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.

Interventions

DRUGBortezomib

Self-administration of subcutaneously Velcade.

Sponsors

Karin B. Ø. Dieperink
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Patients experience of self-administration of VelcadeThrough study completion, from 01. dec. 2019 until 01. jun. 2022Qualitative interviews with all 10 included patients

Secondary

MeasureTime frameDescription
Organizational perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022Patients and health professionals (including pharmacy staff) registration of time spend on treatment on all 10 included patients.
Health care perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022Focus group interview with healthcare professionals involved in the treatment.
Financial perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022Evaluation of financial savings on home treatment including healthcare salaries and transportation.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026