Cognitive Bias Modification: Exploring the effects of a computer-based cognitive bias training in oncology patients at risk for depression and anxiety symptoms -(OncoCogTrain)

Completed

• Conditions: niet-specifieke kanker; chemotherapy; cancer

• Registration Number: NL-OMON46229
• Lead Sponsor: Radboud Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 120

Inclusion Criteria

- Receiving current cancer treatment
- Patients with a score of 8 or higher in the HADS will be considered for participation in the study (HADS; Zigmond & Snaith, 1983). This cut-off shows good sensitivity and specificity in a somatic patient population (Bjelland et al., 2002).
- Signed informed consent form

Exclusion Criteria

- Impossibility to obtain a valid informed consent
- Insufficient comprehension of the Dutch language
- IQ estimate < 80 points

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary objective of our study is to measure changes in depressive and<br /><br>anxiety symptoms from pre to post CBM training. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Our secondary aim is to explore patient*s psychological- and cognitive<br /><br>processes, and course of oncology treatment as factors of our intervention.</p><br>