| Literature DB >> 32408561 |
Gabriele Nibbio1, Stefano Barlati1,2, Paolo Cacciani2, Paola Corsini2, Alessandra Mosca2, Anna Ceraso1, Giacomo Deste2, Antonio Vita1,2.
Abstract
Impairment in real-world functioning remains one of the most problematic challenges that people with schizophrenia have to face. Various psychosocial interventions have proven to be effective in promoting recovery and improving functioning in schizophrenia; however, their implementation and their effectiveness in routine rehabilitation practice are still objects of study. The present pilot study aimed to assess the feasibility and effectiveness on clinical and real-world outcomes of an integrated treatment protocol composed of stable pharmacological treatment, computer-assisted cognitive remediation and social skills training provided in a rehabilitation center. Predictors of functional improvement were also assessed. Seventy-two patients diagnosed with schizophrenia participated in the study. A significant (p < 0.001) improvement in positive, negative and total symptoms, as well as in global clinical severity and real-world functioning outcomes was observed, with a large effect size in positive and total symptoms, global clinical severity and real-world functioning, and a moderate effect size on negative symptoms. Improvement in total symptoms (p < 0.001) and in global clinical severity (p = 0.007) emerged as individual predictors of functional improvement. These findings, although preliminary, suggest that an integrated, evidence-based treatment program is feasible and effective in a real-world rehabilitation context, and that similar interventions should be further implemented in everyday clinical practice.Entities:
Keywords: cognitive remediation; psychosocial rehabilitation; real-world functioning; schizophrenia; social skills training
Year: 2020 PMID: 32408561 PMCID: PMC7277196 DOI: 10.3390/ijerph17103352
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Characteristics of the sample.
| Variable | |
|---|---|
| N | 72 |
| M(%):F(%) | 47(65.3):25(34.7) |
| Age (Years) | 39.08 ± 11.98 |
| Education (Years of Education) | 10.14 ± 3.19 |
| Age of onset (Years) | 24.84 ± 7.22 |
| Pharmacological treatment dose (CPZ eq., mg) | 1040.87 ± 459.15 |
| Length of stay in the center (Months) | 7.18 ± 2.43 |
CPZ eq.: Chlorpromazine equivalents.
Baseline and discharge values of the functional and clinical measures.
| Measure | Baseline ± SD | Discharge ± SD | Mean Difference ± SD |
|---|---|---|---|
| GAF (Functional outcomes) | 32.92 ± 9.40 | 44.50 ± 8.78 | −11.58 ± 6.62 |
| PANSS Positive (Positive symptoms severity) | 19.44 ± 4.92 | 13.36 ± 4.66 | 6.08 ± 3.48 |
| PANSS Negative (Negative symptoms severity) | 26.24 ± 4.86 | 23.64 ± 4.36 | 2.60 ± 2.75 |
| PANSS Total (Total symptoms severity) | 87.79 ± 12.61 | 71.28 ± 11.83 | 16.51 ± 8.05 |
| CGI-S (Global clinical severity) | 5.17 ± 0.63 | 4.47 ± 0.981 | 0.69 ± 0.55 |
GAF: Global Assessment of Functioning; PANSS: Positive and Negative Syndrome Scale; CGI-S: Clinical Global Impression—Severity.
Comparison between the baseline and discharge values of the functional and clinical measures.
| Measure |
| Cohen’s | |
|---|---|---|---|
| GAF (Functional outcomes) | −14.857 | <0.001 | 1.273 (0.915–1.631) |
| PANSS Positive (Positive symptoms severity) | 14.853 | <0.001 | 1.269 (0.911–1.627) |
| PANSS Negative (Negative symptoms severity) | 8.011 | <0.001 | 0.563 (0.230–0.896) |
| PANSS Total (Total symptoms severity) | 29.213 | <0.001 | 1.350 (0.988–1.712) |
| CGI-S (Global clinical severity) | 10.764 | <0.001 | 0.894 (0.508–1.190) |
GAF: Global Assessment of Functioning; PANSS: Positive and Negative Syndrome Scale; CGI-S: Clinical Global Impression—Severity. Cohen’s ds are reported as absolute values. Positive values reflect a positive treatment effect.
Univariate analyses exploring potential predictors of functional improvement.
| Variable |
| |
|---|---|---|
| Sex | 1.142 | 0.258 |
|
|
| |
| Age (Years) | 0.046 | 0.700 |
| Education (Years of Education) | 0.050 | 0.680 |
| Age of Onset (Years) | −0.249 | 0.042 * |
| Pharmacological treatment dose (CPZ eq., mg) | −0.019 | 0.874 |
| Length of stay in the center (Months) | −0.047 | 0.697 |
| Baseline PANSS Positive (Positive symptoms severity) | −0.105 | 0.380 |
| Baseline PANSS Negative (Negative symptoms severity) | 0.014 | 0.907 |
| Baseline PANSS Total (Total symptoms severity) | −0.144 | 0.226 |
| Baseline CGI-S (Global clinical severity) | −0.047 | 0.692 |
| PANSS Positive Change (Positive symptoms improvement) | −0.337 | 0.004 ** |
| PANSS Negative Change (Negative symptoms improvement) | −0.263 | 0.026 * |
| PANSS Total Change (Total symptoms improvement) | −0.510 | <0.001 ** |
| CGI-S Change (Global clinical improvement) | −0.482 | <0.001 ** |
* p < 0.05, ** p < 0.01; CPZ eq.: Chlorpromazine equivalents; PANSS: Positive and Negative Syndrome Scale. CGI-S: Clinical Global Impression—Severity.
Predictors of functional outcome improvement.
| Individual Predictor | Standardized Beta |
|
| |
|---|---|---|---|---|
| PANSS Total Change (Total symptoms improvement) | −0.402 | −3.699 | <0.001 | 1.152 |
| CGI-S Change (Global clinical improvement) | −0.304 | −2.799 | 0.007 | 1.152 |
| Model | ||||
PANSS: Positive and Negative Syndrome Scale; CGI-S: Clinical Global Impression—Severity; VIF: Variance Inflation Factor.