Bipolar Disorder (BPD) Clinical Trials

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Epigenetic Priming to Enhance Cognitive Training Gains and Neuroplasticity in Middle-age and Older Adults With Past Depression or Bipolar Disorder (EPIC)

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this clinical trial is to investigate the effects of a three-week virtual reality-based cognitive remediation training (VR-CRT) programme in combination with daily intake of a histone deacetylase inhibitor (HDACi) sodium butyrate on cognition in symptomatically stable patients with mood disorders (depression or bipolar disorder). The investigators hypothesize that the VR-based cognitive remediation training (VR-CRT) combined with HDACi butyrate vs. a VR-based control treatment combined with placebo will improve global cognition (primary outcome measure) over three weeks. Secondly, the investigators hypothesize that VR-CRT with placebo will improve cognition relative to the VR control treatment with placebo, although to a lesser extent than VR-CRT with HDACi butyrate. Thirdly, the investigators hypothesize that the HDACi butyrate with VR control treatment will not produce cognitive improvements relative to placebo with VR control treatment. Finally, the investigators hypothesize that the combined treatment (VR-CRT + HDACi butyrate) will enhance neuroplasticity (exploratory outcome) vs. VR control with placebo, as indicated by increase in hippocampal volume and/or memory-related activity shown with structural and functional MRI.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 75
Healthy Volunteers: f
View:

• Confirmed ICD-10 diagnosis of BD or recurrent UD in partial, or full remission (Hamilton Depression Rating Scale-17 items and Young Mania Rating Scale scores ≤14)

• Subjective cognitive complaints (self-reported: COBRA ≥12) or objectively-verified cognitive impairment (measured using Screening for Cognitive Impairment in Psychiatry SCIP: total score or at least two subscores ≥ 0.5 SD below expected norms)

• Fluency in Danish language

Locations
Other Locations
Denmark
Neurocognition and Emotion Across Disorders (NEAD Brain Centre, Copenhagen Affective Disorder Research Centre (CADIC), Psychiatric Centre Copenhagen, Frederiksberg Hospital
RECRUITING
Frederiksberg
Contact Information
Primary
Bjørn Ole Barkholt Nordseth, Ph.D.-student
bjoern.ole.barkholt.nordseth@regionh.dk
+4527134653
Backup
Kamilla Woznica Miskowiak, DMSc, DPhil
kamilla.woznica.miskowiak@regionh.dk
+4522771617
Time Frame
Start Date: 2025-11-14
Estimated Completion Date: 2028-07-01
Participants
Target number of participants: 160
Treatments
Experimental: Group 1/4: VR high intensity + sodium butyrate
VR high intensity: Virtual reality Based Cognitive Remediation Therapy (VR-CRT). The cognitive remediation programme has a duration of three weeks and involves weekly virtual reality-based cognitive training sessions with a therapist accompanied by additional between session homework assignments consisting of cognitively challenging daily life tasks.~In this arm, VR high intensity (VR-CRT) is combined with daily intake of HDACi sodium butyrate.
Active_comparator: Group 2/4: VR high intensity + placebo
VR high intensity (VR-CRT): Same as above.~In this arm, VR high intensity (VR-CRT) is combined with placebo.
Sham_comparator: Group 3/4: VR low intensity + sodium butyrate
VR low intensity: A virtual reality-based control treatment (VR-CT). This alternate treatment programme also has a duration of three weeks and involves one weekly 2-hour session with a therapist.~In this arm, VR-based control treatment (VR-CT) is combined with daily intake of HDACi sodium butyrate.
Sham_comparator: Group 4/4: VR low intensity + placebo
VR low intensity (VR-CT): Same as above.~In this arm, VR-based control treatment (VR-CT) is combined with placebo.
Related Therapeutic Areas
Sponsors
Leads: Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg Hospital

This content was sourced from clinicaltrials.gov