Improving drug adherence in cancer patients through a multidisciplinary consultation program

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the impact of a multidisciplinary consultation program on drug adherence among patients undergoing their first oral anticancer treatment. It focuses on identifying barriers to adherence, such as access to medications, adverse effects, and complex regimens. The study measures drug adherence using the medication possession ratio (MPR) before and after implementing the consultation program. The goal is to enhance medication management and reduce healthcare costs associated with nonadherence.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* French speaking patients with a newly diagnosed or relapsed cancer, regardless of location and introduction of oral anticancer treatment

Exclusion Criteria:

* patients treated with hormone therapy only
* Patient with severe psychiatric disorders
* patient who does not speak the French language

Where it's running

• CHU Amiens
  Amiens, France Recruiting

Study contacts

• Study coordinator: Aurélie terrier-lenglet, DR
• Email: terrier-lenglet.aurelie@chu-amiens.fr
• Phone: 0322087173

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.