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Effects of a Digital Patient Platform (CMyLife) for Patients With Chronic Myeloid Leukemia (CML) on Information Provision, Patient Empowerment, Medication Compliance, Guideline Adherence and Quality of Life

R

Radboud University Medical Center

Status

Completed

Conditions

Neoplasms
Patient Portals
Chronic Myeloid Leukemia
Telemedicine

Treatments

Other: CMyLife

Study type

Interventional

Funder types

Other

Identifiers

NCT04595955
RU_23-08-20_LV

Details and patient eligibility

About

A controlled before-after study is performed in order to gain insights into the effectiveness of the CMyLife platform in terms of medication compliance, guideline adherence, quality of life, information provision and patient empowerment. Participants who agreed to use the CMyLife platform for at least 6 months, were enrolled in the treatment group and participants who did not agree to use the platform were enrolled in the control group. After signing informed consent, participants received a baseline questionnaire by mail. Upon completion of the baseline questionnaire, participants used (intervention group) or did not use (control group) the CMyLife platform for at least 6 months, after which they were asked to complete the post-intervention questionnaire.

Enrollment

99 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Newly diagnosed CML patients in chronic phase CML
  • Participants were treated with first or second line TKI's at the haematology department of the participating hospitals. Patients treated with second line TKI's were only allowed to participate if they switched TKI's as a result of side effects and not if they did not respond to the first line TKI

Exclusion criteria

  • Participants in acceleration phase
  • Participants in blastcrise
  • Participants with planned pregnancy in the study period

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

99 participants in 2 patient groups

Intervention group
Experimental group
Description:
This arm uses the CMyLife platform for at least 6 months
Treatment:
Other: CMyLife
Control group
No Intervention group
Description:
This arm does not use the CMyLife platform

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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