Skip to main content
Clinical Trials/NL-OMON46134
NL-OMON46134
Completed
Not Applicable

Cognitive Bias Modification: Exploring the effects of a computer-based cognitive bias training in patients with acute myeloid leukemia at risk for depression and anxiety symptoms -(HemaCogTrain) - Cognitive bias modification in leukaemia patients

Radboud Universitair Medisch Centrum0 sites20 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Radboud Universitair Medisch Centrum
Enrollment
20
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Subjected to the ward of the department of hematology\-oncology for treatment of a AML
  • \- Hightened level of distress as measured with the \*Distress Thermometer\*. A \*Distress Thermometer\* score of 5 or higher was originally recommended as denoting significant distress necessitating psychosocial referral (National Comprehensive Cancer Network, 2005\). 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 IRB\-approved informed consent form

Exclusion Criteria

  • \- Impossibility to obtain a valid informed consent
  • \- Severe depression or other psychiatric disorders that interfere with the ability to receive a cognitive intervention of 20 minutes per day
  • \- Insufficient comprehension of the Dutch language
  • \- IQ estimate \< 80 points
  • \- Acuteness of symptoms that prevent patient from attentively doing the task 20 min

Outcomes

Primary Outcomes

Not specified

Similar Trials