MedPath

Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.

Completed
Conditions
Multiple Myeloma
Registration Number
NCT05163405
Lead Sponsor
Karin B. Ø. Dieperink
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patients experience of self-administration of VelcadeThrough study completion, from 01. dec. 2019 until 01. jun. 2022

Qualitative interviews with all 10 included patients

Secondary Outcome Measures
NameTimeMethod
Health care perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022

Focus group interview with healthcare professionals involved in the treatment.

Financial perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022

Evaluation of financial savings on home treatment including healthcare salaries and transportation.

Organizational perspectiveThrough study completion, from 01. dec. 2019 until 01. jun. 2022

Patients and health professionals (including pharmacy staff) registration of time spend on treatment on all 10 included patients.

Trial Locations

Locations (1)

Odense University Hospital

🇩🇰

Odense, Denmark

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