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Internet-based treatment of depressive symptoms in patients with tumors inside or outside of the central nervous system.

Completed
Conditions
brain tumor
glioma
10025322
10038716
10029211
Registration Number
NL-OMON39265
Lead Sponsor
Vrije Universiteit Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
300
Inclusion Criteria

Experimental groups:;1: adult (>18 years of age) WHO Grade II low-grade glioma survivors.
Mild to moderate depressive symptoms (CES-D score >=12). Participants have to have access to internet and an email account. ;2: adult (>18 years of age) WHO Grade III and Grade IV high-grade glioma patients with an estimated life expectancy of >3 months. Mild to moderate depressive symptoms (CES-D score >=12). Participants have to have access to internet and an email account. ;Control groups:;1: adult (>18 years of age) WHO Grade II low-grade glioma survivors. Mild to moderate depressive symptoms (CES-D score >=12). Participants have to have access to internet and an email account. ;2: adult (>18 years of age) WHO Grade III and Grade IV high-grade glioma patients with an estimated life expectancy of >3 months. Mild to moderate depressive symptoms (CES-D score >=12). Participants have to have access to internet and an email account. ;3. adult (>18 years of age) patients with hematological malignancies without involvement of the central nervous system. Mild to moderate depressive symptoms (CES-D score >=12). Participants have to have access to internet and an email account. ;4. adult (>18 years of age) patients with non-small cell lung cancer without clinical signs of central nervous system involvement. Mild to moderate depressive symptoms (CES-D score >=12). Participants have to have access to internet and an email account.

Exclusion Criteria

Suicidal intent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Measures are taken at 0 weeks (pre-test) and after conclusion of the<br /><br>intervention at 5 weeks (post-test), at 3 months follow-up and at 6 and 12<br /><br>months follow-up for high-grade glioma patients and at 12 months follow-up for<br /><br>low-grade glioma patients. The primary outcome measure is the change in<br /><br>depressive symptoms as measured by the Center for Epidemiological Studies<br /><br>Depression Scale (CES-D). This is a valid and reliable self-report<br /><br>questionnaire used to measure depressive feelings during the past week. The<br /><br>questionnaire consists of 20 propositions, where the respondent indicates how<br /><br>often this proposition applies to him/her (rarely or never, sometimes,<br /><br>regularly, most of the time or always). The sum score lies between 0 and 60. A<br /><br>higher score indicates more feelings of depression. In the general population,<br /><br>people with a score higher than 16 are considered depressed. </p><br>
Secondary Outcome Measures
NameTimeMethod
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