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Developping a a Brain-controlled Art App to Ease Residual Symptoms of Depression

Developping a a Brain-controlled Art App to Ease Residual Symptoms of Depression

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06098469
Acronym
DEEPBLUE
Enrollment
22
Registered
2023-10-24
Start date
2024-10-10
Completion date
2025-02-28
Last updated
2024-11-26

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

Conditions

Depression

Brief summary

The study evaluate the effect of 10 neurofeedback sessions on the residual symptoms of depressive patients in partial remission.

Interventions

DEVICENeurofeedback sessions

10 Neurofeedback sessions, psychiatric interview (MADRS, QIDS-C16), reverse-correlation task, QIDS-SR16, EQ-5D-5L, motivation assessment

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Subjects aged 25 to 65 included * Information and signed informed consent * Patients with a diagnosis of major depressive episode in remission * MADRS score between 14 and 22 * Patients with residual symptoms as assessed by MADRS items * No cognitive impairment. * Right-handed

Exclusion criteria

* Subjects with legal incapacity or limited legal capacity * Subjects unlikely to cooperate with the study and/or poor cooperation anticipated by the investigator * Pregnant women * Subjects in the exclusion period of another study or is on the national volunteer list. * Subjects with another psychiatric pathology (bipolar mood disorder, psychosis, obsessive-compulsive disorder, addictive pathology, schizophrenia) * Subjects under a protective measure such as guardianship or safeguard of justice.

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the effect of 10 neurofeedback sessions on residual symptoms in depressive patients in partial remissionWeek 10Reduction in MADRS score to \< 8 (complete remission) after 10 neurofeedback sessions, in particular cumulative score less than or equal to 2 for hedonic and fatigue dimensions

Countries

France

Contacts

Primary ContactKarine CHARRIERE, PhD
kcharriere@chu-besancon.fr+333 81218999

Outcome results

None listed

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