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Anti-neoplastic Treatment, Based on PRO Data Reported Through a MHealth App Solution in Multiple Myeloma

T

Thomas Lund

Status

Completed

Conditions

Multiple Myeloma

Treatments

Device: mHealth app

Study type

Observational

Funder types

Other

Identifiers

NCT05724966
Fit for treatment

Details and patient eligibility

About

Pirmary endpoint: to examine the feasibility of using an mHealth app for reporting of side effects instead of a telephone call from the hospital staff together with examining the perspectives of patients with multiple myeloma and healthcare professionals of this new method for reporting side effects, and to assess organizational aspects. Usual procedure to assess side effect prior to cancer treatment with Bortezomib is a telephone call the day before. With this innovative method investigator aimed to give the patient more independence in their daily life and in that way improve their quality of life.

Full description

It is a prospective, clinical, parallel mixed-method design with a quantitative core and a qulitative supplementary component. There will be used a Mhealth app called "My Hospital".

Quantitative data will be acquired from time registrations performed by patients and nurses and will be descriptively analyzed applying a micro-costing approach, using cost data per individual. Qualitative data will be obtained from individual, semi-structured interviews with patients and one focus group interview with healthcare professionals and will be analyzed applying a hermeneutic approach.

Eligible for inclusion were patients with MM scheduled for Bortezomib. Moreover, patients should have access to a smartphone, be able to self-report side effects of Bortezomib using a smartphone app, and be willing to participate in a semi-structured interview.

Enrollment

33 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with MM scheduled for Bortezomib
  • patients should have access to a smartphone
  • patients should be able to self-report side effects of Bortezomib using a smartphone app, and be willing to participate in a semi-structured interview.

Exclusion criteria

  • patients had to talk and read danish

Trial design

33 participants in 1 patient group

Registration of side effects
Description:
patients are to registrer side effects prior to treatment with Bortezomib through an app.
Treatment:
Device: mHealth app

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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