A Recovery-Oriented Program for People with Bipolar Disorder through Virtual Reality-Based Cognitive Remediation: Results of a Feasibility Randomized Clinical Trial

Author:

Perra Alessandra12ORCID,Galetti Alessia2,Zaccheddu Rosanna2,Locci Aurora2,Piludu Federica2,Preti Antonio3ORCID,Primavera Diego2,Di Natale Lorenzo4,Nardi Antonio Egidio5ORCID,Kurotshka Peter Konstantin6ORCID,Cossu Giulia2ORCID,Sancassiani Federica2ORCID,Stella Giusy7,De Lorenzo Valerio8,Zreik Thurayya9,Carta Mauro Giovanni2ORCID

Affiliation:

1. International PhD in Innovation Sciences and Technologies, University of Cagliari, 09124 Cagliari, Italy

2. Department of Medical Sciences and Public Health, University of Cagliari, 09124 Cagliari, Italy

3. Department of Neuroscience, University of Turin, 10125 Turin, Italy

4. IDEGO Digital Psychology Society, 00133 Rome, Italy

5. Institute of Psychiatry, Federal University of Rio de Janeiro, Rio de Janeiro 21941-901, Brazil

6. Department of General Practice, University Hospital Wuerburg, 12459 Wuerzburg, Germany

7. Department of Mental Health and Pathological Addiction, ASL 5, 00034 Rome, Italy

8. PRoMIND Services for Mental Health, 00133 Rome, Italy

9. Mental Health Service User Association, 11072070 Beirut, Lebanon

Abstract

Background: Cognitive impairment is a frequent consequence of bipolar disorder (BD) that is difficult to prevent and treat. In addition, the quality of the preliminary evidence on the treatment of BD through Cognitive Remediation (CR) with traditional methods is poor. This study aims to evaluate the feasibility of a CR intervention with fully immersive Virtual Reality (VR) as an additional treatment for BD and offers preliminary data on its efficacy. Methods: Feasibility randomized controlled cross-over clinical study, with experimental condition lasting three months, crossed between two groups. Experimental condition: CR fully immersive VR recovery-oriented program plus conventional care; Control condition: conventional care. The control group began the experimental condition after a three months period of conventional care (waiting list). After the randomization of 50 people with BD diagnosis, the final sample consists of 39 participants in the experimental condition and 25 in the control condition because of dropouts. Results: Acceptability and tolerability of the intervention were good. Compared to the waitlist group, the experimental group reported a significant improvement regarding cognitive functions (memory: p = 0.003; attention: p = 0.002, verbal fluency: p = 0.010, executive function: p = 0.003), depressive symptoms (p = 0.030), emotional awareness (p = 0.007) and biological rhythms (p = 0.029). Conclusions: The results are preliminary and cannot be considered exhaustive due to the small sample size. However, the evidence of efficacy, together with the good acceptability of the intervention, is of interest. These results suggest the need to conduct studies with larger samples that can confirm this data. Trial registration: ClinicalTrialsgov NCT05070065, registered in September 2021

Funder

Fondazione di Sardegna

Publisher

MDPI AG

Subject

General Medicine

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