Skip to content

Adherence to Oral Anticancer Treatment Using Electronic Monitoring System

A Pilot Study of Adherence to Oral Anticancer Treatment Using Electronic Monitoring System

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01058044
Enrollment
33
Registered
2010-01-28
Start date
2009-07-31
Completion date
Unknown
Last updated
2012-08-09

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

Conditions

Cancer

Keywords

Cancer, Sunitinib, capecitabine, anastrozole, letrozole, adherence, anticancer treatment

Brief summary

The purpose of this study is to describe adherence to 3 oral anticancer treatment: i) a chemotherapeutic regimen with capecitabine (alone or in association with lapatinib), ii) or sunitinib an tyrosine kinase inhibitor, iii) or an non-steroidal aromatase inhibitor. Moreover, this study is aimed at evaluating the feasibility to use a Medication Event Monitoring System (MEMS®) in order to assess adherence of an oral anticancer treatment delivered by dispensary pharmacy.

Interventions

OTHEREvaluation of adherence to 3 oral anticancer treatment using a Medication Event Monitoring System

Evaluation of adherence using a Medication Event Monitoring System (MEMS®) for oral anticancer treatment delivered by dispensary pharmacy

Sponsors

Centre Jean Perrin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * histologically proven malignant tumor * documented decision of treatment with i) a chemotherapeutic regimen with capecitabine (alone or in association with lapatinib), ii) or sunitinib an tyrosine kinase inhibitor, iii) or an non-steroidal aromatase inhibitor * ambulatory treated subject * Subject who accept to use MEMS monitors to automatically compile their drug dosing histories * Written informed consent

Exclusion criteria

* any severe concomitant wich makes it undesirable for the patient to participate in the study or which would jeopardize adherence with trial protocol * patient who does not agreed to participate the program

Design outcomes

Primary

MeasureTime frame
evaluation of adherence to 3 oral anticancer treatment: i) a chemotherapeutic regimen with capecitabine (alone or in association with lapatinib), ii) or sunitinib an tyrosine kinase inhibitor, iii) or an non-steroidal aromatase inhibitor.everey visit during 6 months

Secondary

MeasureTime frame
evaluation of liberal nurse satisfactioninclusion
resort to healthcare system (oncologist, doctor, nurse, hospital pharmacy, dispensary pharmacy)during 6 months
Patient satisfaction6 months
drug interactionduring 6 months

Countries

France

Outcome results

None listed

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