Studienlage · Detail
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GRADE
Moderat
763 Zitate
Stichproben = 24 Pat.
DauerEinzeldosis, Messung an sechs…
KontrollePlacebo
EndpunktVAMS
Verblindungdoppelblind
DesignRCT (doppelblind, Placebo-kontrolliert)
Cannabinoidcbd
Max. Dosis600.0 mg
Applikationoral
Kernaussage
CBD 600 mg reduzierte die situative Angst, kognitive Beeinträchtigung und negative Selbstaussagen bei SAD-Patienten signifikant gegenüber Placebo.
Zusammenfassung
n=24 treatment-naïve Patienten mit sozialer Angststörung (SAD), CBD 600 mg vs. Placebo vor simuliertem Public-Speaking-Test. CBD-Gruppe zeigte signifikant reduzierte Angst, kognitive Beeinträchtigung und Unbehagen (VAMS, p-Werte nicht spezifiziert); SSPS-N-Scores in CBD-Gruppe nahezu identisch mit gesunden Kontrollen (n=12), während Placebo-Gruppe deutlich höhere Angstwerte aufwies. Prämedikation mit CBD führte zu ähnlicher Stressantwort wie bei Gesunden.
P
PopulationBehandlungsnaive Patienten mit Generalisierter Sozialer Angststörung (SAD), n=24 (CBD: n=12, Placebo: n=12), zusätzlich gesunde Kontrollen ohne Medikation n=12
I
InterventionEinmaldosis CBD 600 mg oral, 1,5 h vor dem Simulated Public Speaking Test (SPST)
C
KontrollePlacebo (Einmaldosis, doppelblind)
O
OutcomeCBD reduzierte signifikant Angst, kognitive Beeinträchtigung und Unbehagen während der Rede sowie Alertness in der Antizipationsphase (VAMS); SSPS-N-Anstieg unter CBD nahezu aufgehoben vs. Placebo
Vertrauen in die Evidenz
Moderat
Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.
Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
★★★★★
Verblindung
Doppelblind
Effektstärke
Klarer Nutzen
Zitate / Jahr
★★★★★
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Abstract
Generalized Social Anxiety Disorder (SAD) is one of the most common anxiety conditions with impairment in social life. Cannabidiol (CBD), one major non-psychotomimetic compound of the cannabis sativa plant, has shown anxiolytic effects both in humans and in animals. This preliminary study aimed to compare the effects of a simulation public speaking test (SPST) on healthy control (HC) patients and treatment-naive SAD patients who received a single dose of CBD or placebo. A total of 24 never-treated patients with SAD were allocated to receive either CBD (600 mg; n=12) or placebo (placebo; n=12) in a double-blind randomized design 1 h and a half before the test. The same number of HC (n=12) performed the SPST without receiving any medication. Each volunteer participated in only one experimental session in a double-blind procedure. Subjective ratings on the Visual Analogue Mood Scale (VAMS) and Negative Self-Statement scale (SSPS-N) and physiological measures (blood pressure, heart rate, and skin conductance) were measured at six different time points during the SPST. The results were submitted to a repeated-measures analysis of variance. Pretreatment with CBD significantly reduced anxiety, cognitive impairment and discomfort in their speech performance, and significantly decreased alert in their anticipatory speech. The placebo group presented higher anxiety, cognitive impairment, discomfort, and alert levels when compared with the control group as assessed with the VAMS. The SSPS-N scores evidenced significant increases during the testing of placebo group that was almost abolished in the CBD group. No significant differences were observed between CBD and HC in SSPS-N scores or in the cognitive impairment, discomfort, and alert factors of VAMS. The increase in anxiety induced by the SPST on subjects with SAD was reduced with the use of CBD, resulting in a similar response as the HC.
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