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Cognitive Flexibility in Major Depression in the Course of Pharmacological and Psychotherapeutic Treatment

Cognitive Flexibility and Its Correlation to Sleep and Neuroplasticity In The Course Of Depression During Different Treatments

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00993876
Acronym
Decoflex
Enrollment
45
Registered
2009-10-14
Start date
2005-08-31
Completion date
2008-08-31
Last updated
2009-10-14

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

Conditions

Cognitive Performance in Major Depression

Keywords

Depression, CREB, cognitive performance, psychotherapy, SSRI, SNRI

Brief summary

Cognitive deficits in major depression seem explicable by the well-recognized concept of impaired neuroplasticity in mood disorders. This concept initially emerged from preclinical evidence that antidepressants phosphorylate and therefore activate the cyclic AMP response element binding protein (CREB) that is essential for synaptic plasticity. Nevertheless, the question remains whether the activation of CREB by antidepressants is relevant for the remission of cognitive deficits in patients. We addressed this issue by investigating the cognitive improvement during treatment with either citalopram or reboxetine because these antidepressants are different in their capacity to increase phosphorylated CREB (pCREB). Besides the pharmacological treatment groups, another group of patients was treated exclusively with psychotherapy.

Detailed description

We randomly assigned forty-five depressive patients to one of three treatment groups (Citalopram, Reboxetin or interpersonal psychotherapy (IPT)). At baseline, day 7 and day 28 we assessed the severity of depression and the cognitive performance with respect to cognitive flexibility, memory and attention. We measured pCREB with an enzyme linked immuno sorbent assay (ELISA).

Interventions

DRUGcitalopram

20 to 30 mg per day for 4 weeks

4 to 8 mg per day for 4 weeks

BEHAVIORALinterpersonal psychotherapy

Sponsors

German Research Foundation
CollaboratorOTHER
Zentrum für Integrative Psychiatrie
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed according DSM-IV criteria as suffering from major depressive disorder * A baseline score of at least 18 in the Hamilton Depression Scale (HAMD) * No psychopharmacological treatment at least one week prior inclusion or 3 days wash-out

Exclusion criteria

* Severe depressive episode and/or psychotic depressive episode Axis I disorder: * Substance-related Disorders * Psychotic Disorders * Dementia or other cognitive Disorders * Obsessive-Compulsive Disorders Axis II disorder: • Borderline Personality Disorder Axis III disorder: * Infectious Diseases * Cancer * Endocrinological Diseases * Hematological Diseases * Autoimmune Diseases

Design outcomes

Primary

MeasureTime frame
cognitive performance with respect to cognitive flexibility, memory and attention4 weeks

Secondary

MeasureTime frame
CREB-phosphorylation in T-Lymphocytes4 weeks

Countries

Germany

Outcome results

None listed

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