Piloting a Novel, Mobile Cognitive Training Tool for Patients With Major Depressive Disorder (MDD)
Status: | Active, not recruiting |
---|---|
Conditions: | Depression, Depression, Major Depression Disorder (MDD) |
Therapuetic Areas: | Psychiatry / Psychology, Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - 85 |
Updated: | 2/27/2019 |
Start Date: | September 2015 |
End Date: | June 2019 |
To assess the efficacy of a mobile-device-deployed cognitive emotional treatment for
depression (Moodify) versus an active control treatment (commercially available computer
games).
depression (Moodify) versus an active control treatment (commercially available computer
games).
The study will involve a randomized, controlled, double-blind trial to assess the efficacy of
a mobile-device-deployed cognitive emotional treatment for depression (Moodify) versus an
active control treatment (commercially available computer games). Moodify is comprised of a
novel continuous performance task (CPT) to improve cognitive slowing and lethargy often
present in cases of major depressive disorder. This training method is based on an existing,
validated cognitive training paradigm (tonic and phasic attention training, TAPAT1; WIRB
Study No. 1126399). Moodify will also employ two additional cognitive training modules
previously validated in this and other clinical populations.
a mobile-device-deployed cognitive emotional treatment for depression (Moodify) versus an
active control treatment (commercially available computer games). Moodify is comprised of a
novel continuous performance task (CPT) to improve cognitive slowing and lethargy often
present in cases of major depressive disorder. This training method is based on an existing,
validated cognitive training paradigm (tonic and phasic attention training, TAPAT1; WIRB
Study No. 1126399). Moodify will also employ two additional cognitive training modules
previously validated in this and other clinical populations.
Inclusion Criteria:
- Participants must 18 to 85 years or older and not pregnant
- Participants must be fluent in English
- Participants must be able to engage with computerized cognitive tasks as required in
order to participate in this study.
- Normal vision (or corrected to normal vision)
- Participants must be willing to commit to the time requirements of the study as
evidenced by written, informed consent.
- Participants must meet diagnostic criteria for MDD
Exclusion Criteria:
- Participants report or present a hand tremor that prevents the use of a computer mouse
or keyboard
- Participants unable to perform neuropsychological evaluations
- Participants cannot comprehend or follow instructions
- Participants not capable of giving informed consent
- Participants who appear to be intoxicated or under the influence of a controlled
substance
- Participants with a history of significant medical diseases or multiple neurological
events of the head
- Participants with serious or unstable medical illness (e.g. cardiovascular, hepatic,
renal, endocrine, neurologic disease)
- Participants with a history or current diagnosis to specific Diagnostic and
Statistical Manual (DSM)-IV psychiatric illness such as (but not limited to): organic
mental disorder, schizophrenia, schizoaffective disorder, delusional disorder,
psychotic disorder Not Otherwise Specific, bipolar disorder, substance dependence and
substance abuse
- Participants with a history of seizure disorder
We found this trial at
1
site
Click here to add this to my saved trials