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Clinical Trials/ACTRN12609000683235
ACTRN12609000683235
Recruiting
未知

Evaluation of a Web-Based Cognitive Rehabilitation Programme in Cancer Survivors with Self Reported Cognitive Impairment

Dr Janette Vardy0 sites280 target enrollmentAugust 11, 2009

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr Janette Vardy
Enrollment
280
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 11, 2009
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr Janette Vardy

Eligibility Criteria

Inclusion Criteria

  • 1\. Diagnosis of a primary malignancy for which definitive treatment was performed.
  • 2\. Completed a minimum of 3 cycles of potentially curative chemotherapy within the last 6\-60 months.
  • 3\. Aged 18 years and above.
  • 4\. Self reported changes in memory and concentration as per the European Organisation for Research and Treatment of Cancer\-Quality of Life Questionnaire –C30 Cognitive Functioning scale (EORTC\-CF)
  • 5\. Speak fluent English and read to a year 8 standard.
  • 6\. Give written informed consent.
  • 7\. Radiotherapy and/or immunotherapy (e.g. trastuzumab, lapatinib, bevacizumab or cetuximab) (if received) must have been completed at least 12 weeks prior to randomisation.
  • 8\. Hormonal treatment (including tamoxifen or an aromatase inhibitor) is permitted providing treatment has been commenced at least 4 weeks prior to randomisation. Change of hormonal therapy should not be anticipated within the next 6 months, nor should it be likely to be ceased within 6 months.
  • 9\. Easy access to computer and internet facilities.
  • 10\. Participants are expected to be able to complete the study and be available for follow up.

Exclusion Criteria

  • 1\. Eastern Cooperative Oncology Group (ECOG) Performance Status of \> 2\.
  • 2\. Any evidence of locally recurrent or metastatic disease.
  • 3\. Any active psychiatric diagnosis or history of a cognitive disorder. Psychotropic medications are permitted if the patient is established on a stable regime and dosing schedule.
  • 4\. Pre\-existing neurological condition or any other co\-morbidity, which would interfere with their ability to perform cognitive testing.
  • 5\. Prior malignancy within the last 5 years (other than non\-melanomatous skin cancer, cervical cancer in\-situ and the cancer of interest for which they received their chemotherapy).
  • 6\. Any previous chemotherapy other than that given for the cancer of interest.

Outcomes

Primary Outcomes

Not specified

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