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Oral Therapies in Oncology: Cognitive Function and Compliance

C

Centre Francois Baclesse

Status

Terminated

Conditions

Cognitive Function
Oral Therapies
Compliance
Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT01597284
COG-OBS

Details and patient eligibility

About

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

Enrollment

129 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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