Perspectives of Subcutaneous Velcade at Home of Patients With Myeloma.

NCT ID: NCT05163405

Last Updated: 2025-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-12-01

Study Completion Date

2022-06-01

Brief Summary

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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

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Conditions

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Multiple Myeloma

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Interventions

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Bortezomib

Self-administration of subcutaneously Velcade.

Intervention Type DRUG

Other Intervention Names

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Velcade

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Karin B. Ø. Dieperink

OTHER

Sponsor Role lead

Responsible Party

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Karin B. Ø. Dieperink

Nurse, PhD, Associate Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Karin Brochstedt Dieperink, RN

Role: STUDY_DIRECTOR

Odense University Hospital. Department of Oncology.

Locations

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Odense University Hospital

Odense, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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Velcade at home

Identifier Type: -

Identifier Source: org_study_id

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