Cancer and Disorders of Cognitive Functions and Quality of Life: "Cognitive Rehabilitation in Patients Suffering From Cancer and Treated With Chemotherapy"
18 Years
N/A
Both
Cancer
Trial Information
Cancer and Disorders of Cognitive Functions and Quality of Life: "Cognitive Rehabilitation in Patients Suffering From Cancer and Treated With Chemotherapy"
The main objective of our study was to evaluate, in patients treated for cancer expressing
the cognitive complaint during or after treatment, interest workshops on improving cognitive
rehabilitation felt their cognitive functions and their quality of life.
The primary endpoint was the proportion of patients showing an improvement in the score of
perceived deficiencies (score ranging from 0 to 72) of the FACT-Cog after treatment. The
FACT-Cog is a self-administered questionnaire assessing the patients felt their cognitive
difficulties (memory, attention, concentration) and the impact of these difficulties on
their quality of life. The improvement is defined as an increase of 7 points >= cognitive
score won by the (a) patient (e) after the treatment
Inclusion Criteria:
- Patients older than 18 years
- Solid tumor or haematological
- Chemotherapy and / or targeted therapy in the adjuvant or metastatic
- Sequential processing
- Complaints to subjective cognitive during or after (within one year after the end of
chemotherapy and / or targeted therapy) treatment assessed by four items of FACT-COG
(impact on quality of life). Score ≥ 4/16 questions Q35, Q37, Q38 and Q41 of FACT COG
- Patient in remission or pause therapeutic
- Lack of personality disorders and / or psychiatric disorder scalable
- No known brain metastases
- Lack of primary brain tumor
- Lack of analgesic treatment with opioids or Class 3
- Having signed informed consent to participate in the study
- Mastery of the French language
Exclusion Criteria:
- Primary cancer of the central nervous system or brain metastases
- Pathology malignant hematologic
- Disorders of higher functions documented
- Pathology psychiatric scalable
- Use documented drug
- Patient or opioids analgesics in Class 3
- Consumption of alcohol
- Patient unable to respond to cognitive tests and cognitive rehabilitation
- Refusal to participate
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label
Outcome Measure:
Proportion of patients showing an improvement in the score of perceived deficiencies (score ranging from 0 to 72) of the FACT-Cog after care
Outcome Description:
Evaluate, in patients treated for cancer expressing a cognitive complaint during or after the treatment, the interest workshops on improving cognitive rehabilitation felt their cognitive function and quality of life. Autoquestionnary FACT COG
Outcome Time Frame:
up to 3 months
Safety Issue:
No
Principal Investigator
Florence JOLY-LOBBEDEZ, PHD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Centre François Baclesse
Authority:
France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study ID:
COG REDUC
NCT ID:
NCT01788618
Start Date:
July 2012
Completion Date:
June 2015
Related Keywords:
- Cancer
- Cognitive functions
- Quality of life
- Cancer
- Stress, Psychological
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