Use of a Virtual Reality Cognitive Stimulation Programme for Breast Cancer Patients Wishing to Restart or Maintain a Professional Activity (Cog-RV)

C

Centre Francois Baclesse

Status

Not yet enrolling

Conditions

Breast Cancer
Cancer-related Cognitive Difficulties

Treatments

Behavioral: Virtual Reality sessions

Study type

Interventional

Funder types

Other

Identifiers

NCT06267014
2023-A02163-42

Details and patient eligibility

About

The study concerns patients who have been treated for breast cancer, have cognitive problems and are planning to return to work or are currently working and wish to begin cognitive rehabilitation. Patients will follow the Virtual Reality program developed for the study, during the cognitive rehabilitation usually proposed in the establishment, at the rate of a weekly session of 10-15 minute for 6 weeks.

Enrollment

23 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients >18 years of age
  • Patient with breast cancer for whom adjuvant chemotherapy has been administered; maintenance treatments (e.g. Trastuzumab, hormone therapy) are eligible,
  • Maximum 2 years after completion of adjuvant treatment,
  • Patients who have cognitive complaints at inclusion (answer yes to the question: 'Since your cancer treatment, have you had any difficulties with memory, concentration, etc.?)
  • Patients planning to return to work or who have returned to work in the past year,
  • Signature of informed consent prior to any specific procedure relating to the study,
  • Patient affiliated to a social security system.

Exclusion criteria

  • Patients suffering from illnesses or conditions that impair their ability to understand, follow and/or comply with study procedures,
  • Patients with personality disorders and/or psychiatric pathology,
  • Patients deprived of their liberty or placed under the authority of a guardian,
  • Pregnant women

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

23 participants in 1 patient group

Virtual Reality sessions
Experimental group
Treatment:
Behavioral: Virtual Reality sessions

Trial contacts and locations

1

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Central trial contact

Marie LANGE, neuropsychologist; Adeline MOREL, MD

Data sourced from clinicaltrials.gov

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