Clinical Trials Directory

Trials / Unknown

UnknownNCT00256425

Cognitive Rehabilitation of Glioma Patients

Cognitive Rehabilitation of Glioma Patients: a Prospective, Randomized Study

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
140 (actual)
Sponsor
UMC Utrecht · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether cognitive rehabilitation is effective in patients with gliomas (brain tumour), by comparing direct and follow-up neuropsychological functioning and quality of life of the experimental group to the control group.

Detailed description

The majority of patients with (low-grade) glioma exhibit cognitive symptoms and objective deficits, which have a sustained, negative impact on daily functioning and quality of life. Adult patients with a low-grade glioma, either histologically proven, or suspected (1), as well as adult anaplastic glioma patients with favorable prognostic factors (2), who are clinically stable for at least 6 months, will be recruited from 9 hospitals in the Netherlands. Consenting patients with both subjective cognitive symptoms and objective deficits will be randomized to either the cognitive rehabilitation program (N = 75) or a "waiting-list" control group (N = 75). Upon completion of the study, those patients assigned to the control group will be given the opportunity to undergo the cognitive rehabilitation program. The cognitive rehabilitation program incorporates both retraining of impaired cognitive functions, and teaching of compensatory strategies. Rehabilitation will be directed towards attention, memory and executive functioning. The intervention will consist of 6 weekly, individual, 2-hour sessions plus two hours of homework. To evaluate the efficacy of the rehabilitation program, objective neuropsychological functioning, self-reported cognitive symptoms and health-related quality of life will be assessed before rehabilitation, directly following rehabilitation, and at 6-month follow-up.

Conditions

Interventions

TypeNameDescription
BEHAVIORALCognitive rehabilitation

Timeline

Start date
2003-10-01
Completion
2007-09-01
First posted
2005-11-21
Last updated
2008-03-21

Locations

9 sites across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00256425. Inclusion in this directory is not an endorsement.