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Cognitive Computer Training in Patients With Depression

Evaluating Cognitive Computer Training as a Tool for Returning Earlier to Work After Depression

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02821975
Enrollment
20
Registered
2016-07-04
Start date
2015-12-31
Completion date
2017-10-31
Last updated
2016-07-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Computer Training, Depression in Remission, Returning to Work

Keywords

Depression, Cognitive function, Work

Brief summary

Cognitive impairment plays an important role in functional recovery and leads to long-term sickness absence. Therefore there is a need of a treatment specifically improving cognitive functions. In this pilot study the investigators aim to evaluate the feasibility of using cognitive computer training in patients with unipolar depression to enhance cognitive performance. Further the investigators investigate whether this intervention shortens sick leave.

Detailed description

This study will evaluate cognitive computer training on patients in remission from depression by measuring the compliance and effect, investigating whether patients returned earlier to work and examine patients' physical and psychological health. This is done by comparing an intervention group and a control group. Outpatients from psychiatric department Odense in Denmark will be recruited from December 2015 to July 2017. At enrolment the participants wil be randomized 1:1 to either the intervention group or the control group. After the participants will complete a clinical interview and answer the The Short Form (36) Health Survey (SF-36) questionnaire. The participants' cognitive function and depression severity will be measured at baseline and three months follow-up. At nine months follow-up the participants will receive an email with the SF-36 questionnaire and questions about their education and work status, which they were required to answer. The intervention is a cognitive computer program, consisting of different computer games. The intervention will start at enrolment and finish at the three months follow-up. The participants in the intervention group will do trainings session lasting 10-20 minutes three times a week. Each participant ends up with a total of 36 training sessions.

Interventions

OTHERCognitive computer training

COGNIFIT is cognitive computer training. Its purpose is to improve cognitive function and is designed to accommodate each individual's cognitive strengths and weaknesses. The cognitive computer training last three months and must be done three times a week, in session lasting 10-20 minutes.

Sponsors

University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 63 Years
Healthy volunteers
No

Inclusion criteria

* a diagnosis of a moderate to severe unipolar depression according to the International Classification of Diseases -10 criteria * receiving antidepressant medicine * completed their treatment for depression * not be in any risk of suicide * study or work on reduced hours, be unemployed or on long-term sickness leave at enrolment.

Exclusion criteria

* neurological disease of the central nervous system * alcohol or substance abuse * pregnancy * receiving disability pension * receiving electroconvulsive therapy within the last 6 weeks.

Design outcomes

Primary

MeasureTime frameDescription
Employment status of the participants at nine months follow-upWhen the study is completed, approximately 15 monthsQuestionnaire about employment status and will be send to the participants via email at nine months follow-up. The questionnaire include questions according to: current working situation; why they are not working; when they started working; do they work at the same workplace; do they have the same work assignments as before they got ill; do whey work the same number of hour as before the got ill.

Secondary

MeasureTime frameDescription
The difference in working memory from baseline to 3 months follow-up in the intervention group compared to the control group.approximately nine monthsWorking memory is measured by The Letter Number Sequencing
The difference in learning from baseline to 3 months follow-up in the intervention group compared to the control group.approximately nine monthsLearning is measured by the Rey Auditory Verbal Learning Test.
The difference in executive function from baseline to 3 months follow-up in the intervention group compared to the control group.approximately nine monthsExecutive function is measured by The Verbal Fluency
The difference in psychomotor speed from baseline to 3 months follow-up in the intervention group compared to the control group.approximately nine monthsPsychomotor speed is measured by The Trial Making Test (TMT).
The difference in concentration from baseline to 3 months follow-up in the intervention group compared to the control group.approximately nine monthsConcentration is measured by The Digit Span Test
The difference in attention from baseline to 3 months follow-up in the intervention group compared to the control groupapproximately nine monthsAttention is measured by The Letter Cancellation Test

Other

MeasureTime frameDescription
The difference in depression severity from baseline to 3 months follow-up in the intervention group compared to the control group.approximately nine monthsThe depression severity is measured by Hamilton Rating Scale for Depression (17-items)
Compliance of cognitive computer trainingapproximately nine monthsThe participants were supposed to do 36 sessions of cognitive computer training during three months. The actual completed trainings sessions are available on the website of the cognitive computer training, called COGNIFIT. The compliance is defined as the percentage of actual completed training sessions of the 36 sessions of training.
The difference in health status from baseline to 9 months follow-up in the intervention group compared to the control group.approximately 15 monthsThe health status is measured by a patient-reported survey called the The Short Form (36) Health Survey (SF-36) questionnaire

Countries

Denmark

Contacts

Primary ContactAnja F Elliott, BACH.MED.
anjaelliott@hotmail.com+45 60 79 57 24
Backup ContactMorten D Hell, cand.psych.
Old.Morten.Dvoracek.Hell@rsyd.dk+45 28 86 49 19

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026