Remediation for Mild Cognitive Deficits After Cancer

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-12-17

Study Completion Date

2025-07-17

Brief Summary

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Cancer survival rates have improved significantly over the past decades and patients now experience a number of side effects including cancer-related cognitive impairment (CRCI): problems with memory, executive function, attention, and difficulties performing two tasks at the same time. The frequency of CRCI in cancer patients is estimated to be between 10 to 40%, and more than 50% of patients describe difficulties in their daily life. These cognitive difficulties negatively impact the patient's quality of life as well as that of their family, and can also have negative consequences for their social and professional reintegration once cancer treatment is finished. Despite an increasing number of studies on CRCI, a standard of care for patients with CRCI after breast cancer is yet to be established. In the absence of clear directives, and in an attempt to respond to the increasing demand to provide care for breast cancer patients with CRCI, physical medicine and rehabilitation units in France have started providing day-hospital multidisciplinary interventions. The objective of this project is to use the single case experimental design method to investigate the efficacy of two such rehabilitation programs: a group-based program and a one-on-one program.

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Detailed Description

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Conditions

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Cognitive Remediation Breast Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Group-based cognitive remediation program

Patients are admitted to the day hospital 2 days a week for 6 weeks and participate in a group-based (4 patients per group) rehabilitation program conducted by a multidisciplinary team including a PMR doctor, a neuropsychologist, an occupational therapist, and a physical activity monitor).

Group Type EXPERIMENTAL

Cognitive remediation program

Intervention Type BEHAVIORAL

Evaluation of REmediation programs for patients suffering from mild cognitive deficits after Cancer

One-on-one cognitive remediation program

Patients are admitted to the day hospital 5 days a week for 6 weeks and participate in a one-on-one intensive rehabilitation program conducted by a multidisciplinary team including a speech therapist, neuropsychologist, occupational therapist, physiotherapist, physical activity monitor and a psychologist.

Group Type EXPERIMENTAL

Cognitive remediation program

Intervention Type BEHAVIORAL

Evaluation of REmediation programs for patients suffering from mild cognitive deficits after Cancer

Interventions

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Cognitive remediation program

Evaluation of REmediation programs for patients suffering from mild cognitive deficits after Cancer

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Treated in the past for breast cancer with chemotherapy, surgery, and / or radiotherapy,
* Admitted as a day patient at the Henry Gabrielle Hospital or the Pontchaillou CHU Hospital during the study,
* Given free, informed consent in writing after being informed orally and in writing of the how the study will proceed.

Exclusion Criteria

* Presence of another active cancer,
* Ongoing chemotherapy and/or radiotherapy treatment,
* Active progression of breast cancer,
* History of neurological or psychiatric conditions,
* Major disturbances in comprehension that prevent them giving free, informed consent,
* Pregnant, parturient or breastfeeding women,
* Person under a legal protection measure such as guardianship or curatorship,
* People not affiliated to a social security scheme (French Social Security) or beneficiaries of a similar scheme.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No