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| Name | Class |
|---|---|
| University of Lausanne Hospitals | OTHER |
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The objective of this study is to simultaneously establish the metrological characteristics of the new executive function markers (decision making and multiple flow management) derived from repeated ERP variations and to identify their ability to test whether a short treatment using Ginkgo biloba versus placebo extracts can modify the cognitive performance and functional capacity of patients in the very early stages of age-related cognitive decline. This trial, using subjects as their own control (cross-over) in repeated measurements will establish the reproducibility characteristics of the measurements and intra-individual variations of ERP over time in this population
This study is a single-center, randomized clinical trial testing the effects of Ginkgo biloba extracts versus placebo on event related potential ERP registration measurements in Electroencephalography (EEG) during neuropsychological tasks. The Hold-Release (HR) neuropsychological test allows the study of behavioral and neurofunctional correlates using several different techniques for online recording of brain activity. This test measures the engagement of focused attention and the loading of information into working memory, as opposed to the disengagement of attention.
The study will be carried out in a randomized cross-over design, with "Ginkgo" vs. Placebo", or inversely, for 170 days each (approximately 6 months), separated by an 8-weeks wash-out period. A follow-up visit will be held 3 months after the last treatment of the study.
The cross-over design uses each patient as its own control, which allows an easy comparison between the 2 groups "Placebo" vs. "Ginkgo" by limiting inter-patient variations. In addition, by doubling the number of patients per treatment compared to a classic study design in 2 groups, cross-over reduces the number of patients to be recruited, which facilitates recruitment on a single site.
The study requires the recruitment of sixteen (16) informative participants with cognitive complaints.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group Ginkgo-Placebo | Other | Cross-over design: In Group Ginkgo-Placebo participants are allocated first to the IMP Symfona® during 6 months and after 2 months of wash-out period are allocated to the placebo for 6 months. |
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| Group Placebo-Ginkgo | Other | Cross-over design:In Group Placebo-Ginkgo participants are allocated first to the placebo during 6 months and after 2 months of wash-out period are allocated the IMP Symfona® for 6 months. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ginkgo biloba extract | Drug | Symfona® commercial standardized Ginkgo biloba extracts are used in this study, at a rate of 2 capsules of 120 mg per day for 170 days. |
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| Measure | Description | Time Frame |
|---|---|---|
| Reproducibility of contingent negative variation (CNV) event-related potential (ERP) component amplitude (microV) during the Hold-Release (HR) neuropsychological test | Reproducibility of CNV will be assessed by interclass correlation coefficient (ICC) | through study completion, an average of 14 months |
| Intra-individual variability of contingent negative variation (CNV) event-related potential (ERP) component amplitude (microV) during the Hold-Release (HR) neuropsychological test | Intra-individual variability of CNV will be assessed by Interclass Coefficient Correlation (ICC) | through study completion, an average of 14 months |
| Reproducibility of P300/P300' event-related potential (ERP) component amplitude (microV) during the Hold-Release (HR) neuropsychological test | Reproducibility of P300/P300' will be assessed by Interclass Coefficient Correlation (ICC) | through study completion, an average of 14 months |
| Intra-individual variability of P300/P300' event-related potential (ERP) component amplitude (microV) during the Hold-Release (HR) neuropsychological test | Intra-individual variability of P300/P300' will be assessed by Interclass Coefficient Correlation (ICC) | through study completion, an average of 14 months |
| Change in cognitive performance as assessed by variation in amplitude (mivroV) of the CNV component measured during the Hold-Release (HR) neuropsychological test after 6 months of Ginkgo biloba treatment | the statistical model of repeated measurements of variance analysis will be used | through study completion, an average of 14 months |
| Change in cognitive performance as assessed by variation in amplitude (mivroV) of the P300/P300' component measured during the Hold-Release (HR) neuropsychological test after 6 months of Ginkgo biloba treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Change in cognitive performance as assessed using the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) test after 6 months of Ginkgo biloba treatment | the statistical model of repeated measurements of variance analysis will be used | 6 months |
| Change in scores of categorical semantic verbal fluency after 6 months of Ginkgo biloba treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Predictive metrological characteristics of ERP modulation in term of its ability to detect a more sensitive cognitive variation than usual method | a mixed linear model approach will be applied to assess prediction | through study completion, an average of 14 months |
| Predictive metrological characteristics of ERP modulation in term of its ability to detect a slope break during cognitive decline |
Inclusion Criteria
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jean-François Démonet, Prof | Universitary Lausanne Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Leenaards de la mémoire (CLM) CHUV | Lausanne | Canton of Vaud | 1011 | Switzerland |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 19067364 | Background | Amieva H, Le Goff M, Millet X, Orgogozo JM, Peres K, Barberger-Gateau P, Jacqmin-Gadda H, Dartigues JF. Prodromal Alzheimer's disease: successive emergence of the clinical symptoms. Ann Neurol. 2008 Nov;64(5):492-8. doi: 10.1002/ana.21509. | |
| 25201166 | Background | Luck T, Luppa M, Matschinger H, Jessen F, Angermeyer MC, Riedel-Heller SG. Incident subjective memory complaints and the risk of subsequent dementia. Acta Psychiatr Scand. 2015 Apr;131(4):290-6. doi: 10.1111/acps.12328. Epub 2014 Sep 9. |
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randomized double-blind crossover design
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Investigational Medicinal Product (IMP), e.g Placebo and Ginkgo Biloba, is located and dispensed by Central Pharmacy.
Only pharmacists are not blinded but they are neither involved in the conduct of the study not the analysis of the results
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| Placebo | Drug | The placebo is presented in the form of capsules of identical mass, color and shape to those of the study product. It is composed of lactose, the excipients present in Symfona® 120 mg and colorants. The dosage is identical to that of the investigational product. |
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the statistical model of repeated measurements of variance analysis will be used |
| through study completion, an average of 14 months |
the statistical model of repeated measurements of variance analysis will be used |
| 6 months |
| Change in scores of verbal fluency letter instruction after 6 months of Ginkgo biloba treatment | the statistical model of repeated measurements of variance analysis will be used | 6 months |
| Change in anxiety and depression as assessed using the Hospital Anxiety and Depression Scale (HAD-A/D) after 6 months of Ginkgo biloba treatment | the statistical model of repeated measurements of variance analysis will be used | 6 months |
| Change in reaction time (ms) during the Hold-Release (HR) neuropsychological test after 6 months of Ginkgo biloba treatment | the statistical model of repeated measurements of variance analysis will be used | 6 months |
| Magnitude of repetition effects (Test-retest Reliability, TTR) on the contingent negative variation (CNV) event-related potential (ERP) component during the Hold-Release (HR) neuropsychological test. | Combination of an analysis of variance (ANOVA) in repeated measurements and an analysis of variance (ANOVA) in correlation analysis will be used to assess respectively differences (microV) between measurement sessions and the existence of shared associations (correlation coefficient). | through study completion, an average of 14 months |
| Magnitude of repetition effects (Test-retest Reliability, TTR) on P300/P300' event-related potential (ERP) component during the Hold-Release (HR) neuropsychological test. | Combination of an analysis of variance (ANOVA) in repeated measurements and an analysis of variance (ANOVA) in correlation analysis will be used to assess respectively differences (microV) between measurement sessions and the existence of shared associations (correlation coefficient). | through study completion, an average of 14 months |
| Association (correlation coefficient) between a transversal measurement of VPN event-related potential (ERP) component during the Hold-Release (HR) neuropsychological test and the conventional verbal fluency scores. | a mixed linear model approach will be applied to assess prediction | through study completion, an average of 14 months |
| Association (correlation coefficient) between a transversal measurement of P300/P300' event-related potential (ERP) component during the Hold-Release (HR) neuropsychological test and the conventional verbal fluency scores. | a mixed linear model approach will be applied to assess prediction | through study completion, an average of 14 months |
| Association (correlation coefficient) between a transversal measurement of VPN event-related potential (ERP) component during the Hold-Release (HR) neuropsychological test and evolution of its own value during the participant's follow-up | a mixed linear model approach will be applied to assess prediction | through study completion, an average of 14 months |
| Association (correlation coefficient) between a transversal measurement of P300/P300' event-related potential (ERP) component during the Hold-Release (HR) neuropsychological test and evolution of its own value during the participant's follow-up | a mixed linear model approach will be applied to assess prediction | through study completion, an average of 14 months |
a mixed linear model approach will be applied to assess prediction |
| through study completion, an average of 14 months |
| 9811557 | Background | Thierry G, Doyon B, Demonet JF. ERP mapping in phonological and lexical semantic monitoring tasks: A study complementing previous PET results. Neuroimage. 1998 Nov;8(4):391-408. doi: 10.1006/nimg.1998.0371. |
| 20361039 | Background | Martin CD, Thierry G, Demonet JF. ERP characterization of sustained attention effects in visual lexical categorization. PLoS One. 2010 Mar 25;5(3):e9892. doi: 10.1371/journal.pone.0009892. |
| 25114079 | Background | Tan MS, Yu JT, Tan CC, Wang HF, Meng XF, Wang C, Jiang T, Zhu XC, Tan L. Efficacy and adverse effects of ginkgo biloba for cognitive impairment and dementia: a systematic review and meta-analysis. J Alzheimers Dis. 2015;43(2):589-603. doi: 10.3233/JAD-140837. |
| 12895688 | Background | Kennedy DO, Scholey AB, Drewery L, Marsh VR, Moore B, Ashton H. Electroencephalograph effects of single doses of Ginkgo biloba and Panax ginseng in healthy young volunteers. Pharmacol Biochem Behav. 2003 Jun;75(3):701-9. doi: 10.1016/s0091-3057(03)00120-5. |
| ID | Term |
|---|---|
| C063170 | Ginkgo biloba extract |
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