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Oral Therapies in Oncology: Cognitive Function and Compliance

Oral Therapies in Oncology: Cognitive Function and Compliance

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01597284
Enrollment
129
Registered
2012-05-14
Start date
2012-02-29
Completion date
2016-03-31
Last updated
2017-02-10

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

Conditions

Cancer, Cognitive Function, Compliance, Oral Therapies

Keywords

Oral therapies, Cancer, cognitive function, compliance

Brief summary

The investigators propose to evaluate the compliance of oral cancer therapies, particularly the possible link between this observance and cognitive function of patients at initiation of treatment. To our knowledge, this study will be among the first conducted on the issue in France and is an innovative approach in the management of cancer patients. The inclusion of cognitive dysfunction is part of a comprehensive approach to improving the quality of life and fully meets the objectives of both plans cancer, including those of the axis Living during and after cancer highlighted in the Cancer Plan

Interventions

None listed

Sponsors

Centre Francois Baclesse
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age over 18 years, * Patients treated with a first prescription of exclusive oral therapy (chemotherapy and/or targeted therapy) as part of a cancer, * Patients who begin treatment with ZYTIGA ® (abiraterone acetate) are incluables, * Patients with asymptomatic brain metastases are incluables, * Lack of personality disorders and psychiatric illness scalable, * Knowledge of spoken and written French, * Having signed the informed consent of study participation.

Exclusion criteria

* Pathology psychiatric * Refusal to participate, * Patient unable to respond to cognitive tests, - Documented use of drugs, * Heavy drinking, - Cancer primitive central nervous system, - Participation in a clinical trial.

Design outcomes

Primary

MeasureTime frame
Assess the relationship between cognitive function at baseline oral anti-cancer treatment and adherence to treatment.8 months

Countries

France

Outcome results

None listed

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