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Stimulatie om het geheugen te verbeteren (STIM)

29 juni 2026 bijgewerkt door: Benjamin Hampstead, PhD, University of Michigan

High Definition Transcranial Direct Current Stimulation (HD-tDCS) testen als behandeling van milde cognitieve stoornissen

Deze studie zal de effecten testen van verschillende doses van een vorm van niet-invasieve hersenstimulatie voor de behandeling van personen met milde cognitieve stoornissen (MCI) en dementie van het Alzheimer-type (DAT).

Studie Overzicht

Gedetailleerde beschrijving

Dit onderzoek wordt uitgevoerd om belangrijke informatie te verkrijgen over de effecten van zwakke elektrische stimulatie op het functioneren van de hersenen bij mensen met milde cognitieve stoornissen (MCI) en dementie van het Alzheimer-type (DAT). De bevindingen zullen helpen bepalen "hoeveel" stimulatie nodig is om het geheugen en denkvermogen te verbeteren, hoe het de werking van de hersenen beïnvloedt en wie er waarschijnlijk baat bij heeft. Uiteindelijk kan deze informatie de behandelingsinspanningen begeleiden voor mensen in verschillende stadia van de ziekte van Alzheimer. De studie zal hersenbeeldvorming gebruiken om te zien of deze behandelingen de manier veranderen waarop deelnemers informatie leren en onthouden. Functionele magnetische resonantie beeldvorming (fMRI) en positronemissietomografie (PET) scans zullen worden gebruikt. De studie zal ook cognitieve tests en vragenlijsten gebruiken om te onderzoeken of het geheugen van de deelnemers (en gerelateerde vaardigheden) veranderen als gevolg van de behandeling. De studie zal deelnemers inschrijven met een diagnose van MCI of DAT. Het wordt verwacht, maar is niet vereist, dat deelnemers mede worden ingeschreven in het University of Michigan Memory and Aging Project (UM-MAP; HUM00000382).

Studietype

Ingrijpend

Inschrijving (Werkelijk)

233

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Michigan
      • Ann Arbor, Michigan, Verenigde Staten, 48105
        • University of Michigan

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

55 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusiecriteria:

  1. Diagnose van milde cognitieve stoornissen (MCI) of dementie van het Alzheimer-type (DAT)
  2. Moet MRI-compatibel zijn, criteria die ook gelden voor High Definition transcraniële gelijkstroomstimulatie (HD-tDCS; bijv. afwezigheid van metalen of elektronische implantaten in het bovenlichaam of hoofd)
  3. Stabiel op relevante medicijnen gedurende ten minste 4 weken voorafgaand aan de studie-inschrijving

Uitsluitingscriteria:

  1. Bepaalde neurologische aandoeningen
  2. Bepaalde psychiatrische aandoeningen
  3. Ernstige zintuiglijke beperking

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verdrievoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Sham-vergelijker: Schijnstimulatie
Sham (placebo) dosis van HD-tDCS-behandeling gedurende 30 minuten, voor tussen de 5-30 sessies.
Deelnemers krijgen schijn (placebo) HD-tDCS gedurende 30 minuten, voor tussen de 5-30 sessies.
Experimenteel: 1 mA Dosering Stimulatie
1 milliAmp dosis HD-tDCS-behandeling gedurende 30 minuten, voor tussen de 5-30 sessies.
Deelnemers ontvangen HD-tDCS bij 1 mA gedurende 30 minuten, gedurende 5-30 sessies.
Experimenteel: 2 mA Dosering Stimulatie
2 milliAmp dosis HD-tDCS-behandeling gedurende 30 minuten, voor tussen de 5-30 sessies.
Deelnemers ontvangen HD-tDCS bij 2 mA gedurende 30 minuten, gedurende 5-30 sessies.
Experimenteel: 3 mA Dosering Stimulatie
3 milliAmp dosis HD-tDCS-behandeling gedurende 30 minuten, voor tussen de 5-30 sessies.
Deelnemers ontvangen HD-tDCS bij 3 mA gedurende 30 minuten, gedurende 5-30 sessies.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Lateral Temporal Cortex Connectivity
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Primary outcome focuses on default mode network (DMN) between-network functional connectivity because the lateral temporal cortex is a core component of the DMN. Between-network functional connectivity is estimated from fMRI data as strength of temporal coupling between the DMN and other high-level (association) brain networks. For each participant and time point, correlation-based connectivity (Pearson r; Fisher r-to-z transformed; arbitrary units) computed between DMN regions and other regions of the association cortex defined using standard functional atlas. Higher values reflect stronger functional connectivity between DMN and other regions. A Z-score's range is infinite. Expected value is between -3 to 3. Analyses conducted separately for amyloid negative (A-) and amyloid positive (A+) participants. Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.
Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Self-Report of Contentment With Memory
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

The Multifactorial Memory Questionnaire (MMQ) consists of three scales measuring separate aspects of metamemory. Items are rated on a 5-point Likert scale (0-4) based on the test taker's experiences over the previous two weeks.

MMQ-Satisfaction (formerly called MMQ-Contentment) scale measures satisfaction, concern, and overall appraisal of one's own memory. Each of 18 statements is rated based on degree of agreement. The score range is 0 to 72, with higher scores indicating a higher degree of satisfaction.

Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Self-Report of Memory Mistakes
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

Multifactorial Memory Questionnaire (MMQ) Ability Score - This scale measures self-perception of everyday memory ability. Respondents rate how often they experienced each of 20 common memory mistakes over the previous two weeks. The score range is 0 to 80, with higher scores indicating better self-reported memory ability.

Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Self-Report of Memory Strategies Used
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

Multifactorial Memory Questionnaire (MMQ) Strategies Score - This scale measures the use of practical memory strategies and aids in day-to-day life. Respondents rate how often they used each of 19 memory strategies over the previous two weeks. The score range is 0 to 76, with higher scores indicating greater use of memory strategies.

Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Change in Memory Functioning
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
The Repeatable Battery of the Assessment of Neuropsychological Status (RBANS) is a comprehensive neuropsychological battery for the evaluation of global cognition. The delayed memory section is a measure of delayed recall and recognition for verbal and visual information. It includes the subtests List Recall, List Recognition, Story Memory, and Figure Recall. Low scores on this index indicate difficulties with recognition and retrieval of information from long-term memory stores This index is composed of both auditory and visual measures; therefore, a severe deficit in language, auditory processing, or visual functioning may impact one of the measures more than the other. Analysis included the sum of the raw scores for each of the delayed memory subtests, with possible scores ranging from 0 to 62. Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.
Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Change in Overall Fluid Cognitive Abilities
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

Cognitive function was determined using the NIH Toolbox-Cognition Battery computerized tests, specifically the Fluid composite score. It is derived by averaging the subtests in the Fluid domain to achieve an overall standard score. Fully Corrected T-scores are adjusted for for age, gender, race/ethnicity, and educational attainment. The score compares the score of the participant to those in the NIH Toolbox nationally representative normative sampling. The T-score has a mean of 50 in the general population and a SD of 10. Scores higher than the mean indicate better performance.

Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Cumulative Working Memory Effects of HD-tDCS Across Treatment Sessions
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

The n-back test is a working memory task where participants identify stimulus that matches stimulus experienced "n" steps back. Participants performed a 2-back test, in which they were asked to remember and press a button when shown a stimulus that appeared 2 steps before the current one (e.g. square, circle, square).

The number of correct and incorrect identifications are normalized (z-score). Total score is the z-score of correct button presses minus the z-score of incorrect button presses. A higher score (d') reflects better working memory performance. Possible scores range from -4.85 to 4.85. Positive change (increase) in 2-back score across treatment sessions indicates improvement in working memory performance. Data is shown as the mean slope calculation of participants across first 5 days of treatment and across all treatments, x=days of treatment, y=n-back score.

Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Cumulative Memory Accuracy Effects of HD-tDCS Across Treatment Sessions
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

Paired Associates task is a verbal memory task that asks participants to learn a list of word pairs. After a delay, participants are shown correct and mismatched word pairs one at a time and asked to identify if the displayed word pair was from the list they were asked to learn or not.

Total accuracy is a proportion (total correct responses divided by total trials completed) ranging from 0 to 1 that measures the accuracy of a participant's responses to both correct and mismatched word pairs. Higher scores indicate better verbal memory performance, and positive changes over time indicate an improvement in verbal memory performance, measured after baseline (Session 1) and every intervention session (Sessions 2-5)

Data is shown as the mean slope calculation of participants across first 5 days of treatment and across all treatments, x=days of treatment, y= total accuracy.

Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Cumulative Memory Sensitivity Effects of HD-tDCS Across Daily Sessions
Tijdsspanne: Baseline
Verbal memory performance for computerized Paired Associates task, summarized with a computational model (linear ballistic accumulator decision model). The model uses each participant's accuracy and reaction times across trials to estimate how efficiently they accumulate information to distinguish previously studied (target) word pairs from new (lure) pairs. Reported outcome is the average memory sensitivity score at baseline, expressed as unitless model values (scores on a scale) where higher scores indicate better discrimination, scores near zero indicate chance-level performance, and negative scores (if present) indicate performance worse than chance.
Baseline
Tolerability of HD-tDCS
Tijdsspanne: Assessed immediately after each HD-tDCS session (participants received up to 30 sessions over approximately 1-12 weeks); values represent mean symptom burden averaged across all post-stimulation assessments
Tolerability was assessed using the HD-tDCS Safety Questionnaire, an 11-item symptom checklist. The questionnaire assesses the presence (yes/no) of 10 specific self-reported symptoms (Itching, Burning, Tingling, Scalp Pain, Trouble Concentrating, Sleep problems, Headache, Mood Change, Neck Pain, and Other symptoms) and 1 oberserved symptom, Skin Redness. Skin Redness was excluded from this analysis as it is not related to the participant's perception of tolerability. The total score (symptom burden) was calculated by summing the number of symptoms present across the 10 items for each session. Score range: 0 to 10 symptoms, where 0 = no symptoms present and 10 = all symptoms present. Higher scores indicate worse tolerability (more symptoms experienced). Values represent the mean number of symptoms per session, calculated by averaging symptom burden scores across all post-stimulation assessments within each treatment group.
Assessed immediately after each HD-tDCS session (participants received up to 30 sessions over approximately 1-12 weeks); values represent mean symptom burden averaged across all post-stimulation assessments
Effectiveness of Blinding of HD-tDCS
Tijdsspanne: Assessed immediately after each HD-tDCS session (participants received up to 30 sessions over approximately 1-12 weeks)
Participant's perception of treatment assignment assessed after each stimulation session using a 3-category ordinal scale. Participants guessed whether they received: (0) Sham stimulation, (1) Don't Know, or (2) Active stimulation. The scale is ordinal with Sham < Don't Know < Active. Effective blinding is indicated by no significant difference in the distribution of perceived assignment between active and sham groups (i.e., participants in active groups cannot reliably distinguish their treatment from sham). Higher proportional odds ratios would indicate active group participants were more likely to guess "active"; lower ratios would indicate sham participants were more likely to guess "active" (paradoxical pattern suggesting convincing sham condition).
Assessed immediately after each HD-tDCS session (participants received up to 30 sessions over approximately 1-12 weeks)
Change in Default Mode Network Connectivity
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

The outcome focuses on default mode network (DMN) within-network functional connectivity. Within-network functional connectivity is estimated from fMRI data as strength of temporal coupling within DMN regions (nodes). For each participant and time point, correlation-based connectivity (Pearson r; Fisher r-to-z transformed; arbitrary units) was computed between DMN regions defined using a standard functional atlas. Higher values reflect stronger functional connectivity within DMN. A Z-score's range is infinite. Expected value is around -3 to 3. Analyses are conducted separately for amyloid negative (A-) and amyloid positive (A+) participants.

Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Cumulative Cognitive Change Across Daily Consecutive Sessions
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Measured through change in Cogstate or other comparable computerized cognitive testing scores across consecutive daily sessions.
Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).
Change in Global Cognition
Tijdsspanne: Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

The Repeatable Battery of the Assessment of Neuropsychological Status (RBANS) is a comprehensive neuropsychological battery for the evaluation of global cognition and has been validated in subjects with mild cognitive impairment, moderate to severe traumatic brain injuries, vascular dementias, and Alzheimer's disease. Data was analyzed using the sum of the subtest raw scores, which is an indicator of the general cognitive functioning of the examinee. Low scores suggest general cognitive impairment even when some individual subtest scores may be within normal limits. Individuals with low scores on this measure exhibit problems with attention, memory, language, and construction skills. Possible scores range from 0 to 321.

Post Intervention data collection was on day 5 of treatment. Post-Expansion (PE) appointments were not consecutive. Mean time between enrollment and PE was 10 wks, longest was 43 wks.

Change from Baseline to Post-Intervention (after tDCS Session 5 - day 5 of treatment) and from Baseline to Post-Expansion (after the participant's final tDCS session beyond Session 5, up to 43 weeks).

Andere uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Verandering in remmingsvermogen
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
A priori intentie om te meten door verandering in de NIH Toolbox Flanker Inhibitory Control en Attention Test Score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in begripsvermogen
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
A priori intentie om te meten door verandering in de NIH Toolbox Dimensional Change Card Sort Test Score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Wijziging in geheugen voor beeldreeksen
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
A priori intentie om te meten door verandering in de NIH Toolbox Picture Sequence Memory Test Score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in werkgeheugenvermogen
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
A priori intentie om te meten door verandering in de NIH Toolbox List Sorting Working Memory Test Score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in verwerkingssnelheid
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
A priori intentie om te meten door verandering in de NIH Toolbox Pattern Comparison Processing Speed ​​Test Score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in visueel-ruimtelijk functioneren
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
Gemeten door verandering in de RBANS Visuospatial Index-score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in taalfunctioneren
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
Gemeten door verandering in de RBANS Language Index-score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in aandacht
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
Gemeten via verandering in de RBANS Attention Index-score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in geheugenfunctie
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
Gemeten via verandering in de RBANS Immediate Memory Index-score
Baseline en post-interventie (na tDCS-sessies 5 & 30)
Verandering in cognitief functioneren
Tijdsspanne: Baseline en post-interventie (na tDCS-sessies 5 & 30)
A priori intentie om te meten via veranderingen in RBANS-subtestscores
Baseline en post-interventie (na tDCS-sessies 5 & 30)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Benjamin Hampstead, PhD, Associate professor

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 april 2019

Primaire voltooiing (Werkelijk)

6 december 2024

Studie voltooiing (Werkelijk)

19 december 2024

Studieregistratiedata

Eerst ingediend

11 maart 2019

Eerst ingediend dat voldeed aan de QC-criteria

13 maart 2019

Eerst geplaatst (Werkelijk)

14 maart 2019

Updates van studierecords

Laatste update geplaatst (Werkelijk)

2 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

29 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Ja

product vervaardigd in en geëxporteerd uit de V.S.

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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