Active — Not RecruitingNot Applicable

Evaluation of Cognitive Management for Chemobrain in Patients Treated for Breast Cancer.

France164 participantsStarted 2023-02-01

Plain-language summary

This project will investigate the efficacy of a cognitive remediation programme in patients treated for breast cancer. patients will be randomized between "no intervention" and "intervention programme". Efficay will be assessed in term of improved quality of life.

Who can participate

Age range20 Years – 60 Years

SexFEMALE

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Inclusion criteria

✓. Women aged 20 to 60 years inclusive.
✓. Localised breast cancer having required neoadjuvant or adjuvant chemotherapy, the last cycle of which took place between 2 and 24 months prior to inclusion.
✓. Informed consent dated and signed.
✓. Patient with French social security cover in accordance with French law on biomedical research (Article 1121-11 of the French code of public health).

Exclusion criteria

✕. Metastatic breast cancer.
✕. Presence of unstable psychiatric or neurological disorders likely to affect cognition (information requested directly from the participant)
✕. History of drug abuse.
✕. Patient who cannot read or understand French.
✕. Patient already included in this study.
✕. Patient having participated in onCOGITE workshops.
✕. Patient participating in another clinical trial evaluating cognitive remediation.
✕. Patient deprived of freedom or subject to legal protection measures (under guardianship, in custody of the court, or family-member guardianship order).

What they're measuring

Number of participants with improved quality of life (Emotional and functional QoL)

Timeframe: 4 months after initiation of the cognitive stimulation protocol using the "onCOGITE" method

Trial details

NCT IDNCT05690828

SponsorInstitut Bergonié

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-10-30

View on ClinicalTrials.gov More Breast Cancer trials