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Trial · NCT05336175

Registered outcomes42

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBaseline Blood Biomarkers - Neurology 4-Pleax A, pTau-181, and pTau 231 as measured by the Quanterix Simoa Neurology 4-plex A and Simoa pTau-181 and 283 advantage kitsThese measurements will be taken at baseline
We will use the Quanterix Simoa Neurology 4-Plex A (N4PA) Advantage kit to measure Neurology 4-Plex A (GFAP, NF-light, Total Tau, UCH-L1 and the Simoa pTau-181 and 283 Advantage kits to measure pTau-181 and pTau 231.
PrimaryBaseline evaluations of associative, verbal memory as measured by the verbal paired associates task (version 2)These measurements will be taken at baselineThe verbal paired associates task (version 2) will be used to evaluate associative, verbal memory. Scores can range from 0 to 36 with higher scores indicating better outcomes.
PrimaryBaseline evaluations of associative, visual memory as measured by the Face Name Associative Memory TestThese measurements will be taken at baselineThe Face Name Associative Memory Test will be used to evaluate associative, visual memory. Scores can range from 0 to 12 with higher scores indicating better outcomes.
PrimaryBaseline evaluations of pattern separation memory as measured by the Mnemonic Similarity TaskThese measurements will be taken at baselineThe Mnemonic Similarity Task will be used to evaluate pattern separation memory. Scores can range from 0 to 1.0 with higher scores indicating better outcomes
PrimaryBaseline evaluations of executive functions - updating/working memory as measured by the Keep Track TaskThese measurements will be taken at baselineThe Keep Track Task will be used to evaluate executive function - updating/working memory. Scores can range from 0 to 30 with higher scores indicating better performance.
PrimaryBaseline evaluations of executive functions - switching as measured by the Number-Letter TaskThese measurements will be taken at baselineThe Number-Letter task will be used to evaluate executive function - switching. Scores can range from 0.2sec to 10 sec with higher scores indicating worse outcomes
PrimaryBaseline evaluations of executive functions - attention/inhibition as measured by the Flanker TaskThese measurements will be taken at baselineThe Flanker Task will be used to evaluate executive function - attention/inhibition. Scores can range from 200ms - 2000ms with higher scores indicating worse outcomes
PrimaryBaseline evaluations of processing speeds - simple/complex processing speeds as measured by the Deary-Liewald Reaction Time TaskThese measurements will be taken at baselineThe Deary-Liewald Reaction Time Task will evaluate processing speed - simple/complex processing speed. Scores can range from 200ms - 1500ms with higher scores indicating worse outcomes
PrimaryBaseline evaluations of reading ability/vocabulary as measured by the North American Reading TestThese measurements will be taken at baselineThe North American Reading Test will be used to evaluate reading ability/vocabulary. Scores can range from 0 to 61 with higher score indicating better outcomes
PrimaryBaseline evaluations of global cognitive functioning as measured by the Montreal Cognitive AssessmentThese measurements will be taken at baselineThe Montreal Cognitive Assessment will be used to evaluate global cognitive functioning/ Scores can range from 0 - 30 with higher scores indicating better outcomes.
PrimaryParticipants sleep quality will be assessed as measured by the Pittsburgh Sleep Quality IndexThese measurements will be taken at baselineThe Pittsburgh Sleep Quality Index will be used to assess sleep quality. Scores can range from 0 to 21 with higher scores indicating worse outcomes
PrimaryParticipants quality of life will be assessed as measured by the World Health Organization Quality of Life - BREF (WHOQOL-BREF)These measurements will be taken at baselineThe World Health Organization Quality of Life - BREF (WHOQOL-BREF) will be used to assess participant's quality of life. Score can range from 3 to 40 with higher scores indicating better outcomes
PrimaryParticipants disability due to health/mental health conditions will be assessed as measured by the World Health Organization Disability Assessment Schedule 2.0These measurements will be taken at baseline
The World Health Organization Disability Assessment Schedule 2.0 will be used to assess participant's disability due to health/mental health conditions. Scores can range from 7 to 36 with higher scores indicating worse outcomes.
PrimaryParticipants physical activity will be assessed as measured by Rapid Assessment of Physical ActivityThese measurements will be taken at baselineThe Rapid Assessment of Physical Activity will be used to assess participant's physical activity. Scores can range from 1 to 10 with higher scores indicating better outcomes.
PrimaryParticipants heart failure health status will be assessed as measured by the Kansas City Cardiomyopathy QuestionnaireThese measurements will be taken at baselineThe Kansas City Cardiomyopathy Questionnaire. Scores can range from 12 to 118 with higher scores indicating better outcomes
PrimaryParticipants independent living skills will be assessed as measured by the Lawton-Brody Instrumental Activities of Daily Living Scale (I.A.D.L)These measurements will be taken at baselineThe Lawton-Brody Instrumental Activities of Daily Living Scale (I.A.D.L). Scores can range from 0 to 8 with higher scores indicating better outcomes.
Primary12-week Blood Biomarkers - Neurology 4-Pleax A, pTau-181, and pTau 231 as measured by the Quanterix Simoa Neurology 4-plex A and Simoa pTau-181 and 283 advantage kitsThese measurements will be taken after the 12 week drug course
We will use the Quanterix Simoa Neurology 4-Plex A (N4PA) Advantage kit to measure Neurology 4-Plex A (GFAP, NF-light, Total Tau, UCH-L1 and the Simoa pTau-181 and 283 Advantage kits to measure pTau-181 and pTau 231.
Primary12-week evaluations of associative, verbal memory as measured by the verbal paired associates task (version 2)These measurements will be taken after the 12 week drug courseThe verbal paired associates task (version 2) will be used to evaluate associative, verbal memory. Scores can range from 0 to 36 with higher scores indicating better outcomes.
Primary12-week evaluations of associative, visual memory as measured by the Face Name Associative Memory TestThese measurements will be taken after the 12 week drug courseThe Face Name Associative Memory Test will be used to evaluate associative, visual memory. Scores can range from 0 to 12 with higher scores indicating better outcomes.
Primary12-week evaluations of pattern separation memory as measured by the Mnemonic Similarity TaskThese measurements will be taken after the 12 week drug courseThe Mnemonic Similarity Task will be used to evaluate pattern separation memory. Scores can range from 0 to 1.0 with higher scores indicating better outcomes

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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