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Working Memory and Physical Exercise Training in Patients With Mild Cognitive Impairment

Offene Rekrutierung
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT05948930 ist eine interventionsstudie zur Untersuchung von Leichte kognitive Beeinträchtigung und hat den Status offene rekrutierung. Die Studie startete am 8. Januar 2024 und soll 90 Teilnehmer aufnehmen. Durchgeführt von Universität von Maryland, Baltimore ist der Abschluss für 7. August 2026 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 11. April 2025 aktualisiert.
Kurzbeschreibung
The prevalence of dementia will double in the next three decades in the U.S.; effective treatment or prevention for dementia is urgently needed. The current exploratory project aims to evaluate and understand how the brain and cognition may improve after a 12-week intervention that combines brain training and aerobic exercise training to improve brain function, both in those with mild cognitive impairment (some with possible prodromal Alzheimer's disease) and with healthy aging. Findings from this pilot project will guide and refine the development of a future larger clinical trial that aligns with the goals of the National Alzheimer's Plan of Action (NAPA), especially regarding "Prevent and Effectively Treat Alzheimer's Disease (AD) by 2025.
Offizieller Titel

Adaptive Working Memory and Physical Exercise Training to Improve Brain and Mitochondrial Function in MCI

Erkrankungen
Leichte kognitive Beeinträchtigung
Publikationen
Wissenschaftliche Artikel und Forschungspapiere zu dieser klinischen Studie:
Weitere Studien-IDs
  • HP-00105789
NCT-Nummer
Studienbeginn (tatsächlich)
2024-01-08
Zuletzt aktualisiert
2025-04-11
Studienende (vorauss.)
2026-08-07
Geplante Rekrutierung
90
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Offene Rekrutierung
Primäres Ziel
Supportivtherapie
Zuteilungsmethode
Nicht randomisiert
Interventionsmodell
Parallel
Verblindung
Einfach verblindet
Studienarme/Interventionen
Teilnehmergruppe/StudienarmIntervention/Behandlung
ExperimentellAerobic Exercise
Progressive aerobic exercise 3x/week for 12 weeks.
Progressive Aerobic Exercise
Progressive aerobic exercise
ExperimentellCognitive Training
Adaptive cognitive training on Cogmed 5x/week for a total of 25 sessions in 5-8 weeks.
Adaptive Cognitive Training
Adaptive cognitive training
ExperimentellCombined Cognitive and Aerobic Exercise
Combined progressive aerobic exercise 3x/week for 12 weeks and adaptive cognitive training on Cogmed 5x/week for a total of 25 sessions in 5-8 weeks simultaneously.
Combined
Combine adaptive cognitive and progressive aerobic exercise training
Hauptergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Changes in Brain structure measures
Changes in brain volume measures from T1-weighted images (volumes in mm3)
At baseline and at 4 weeks after the corresponding training program.
Changes in brain cortical thickness measures
Changes in brain cortical thickness measures from T1-weighted images (thickness measures in mm)
At baseline and at 4 weeks after the corresponding training program.
Changes in Brain microstructure measures
Changes in brain measures of diffused tensor imaging (diffusion coefficient in mm²/s)
At baseline and at 4 weeks after the corresponding training program.
Changes in Brain blood flow from Arterial spin labeling magnetic resonance imaging (ASL-MRI) in milliliters/100 g/minutes
Changes in Brain blood flow from Arterial spin labeling magnetic resonance imaging (ASL-MRI) in milliliters/ 100 g/ minutes
At baseline and at 4 weeks after the corresponding training program.
Changes in Brain Activation on functional MRI
Changes in functional MRI from blood oxygen level dependence (BOLD) contrast on fMRI (in percentage change)
At baseline and at 4 weeks after the corresponding training program.
Changes in cognitive performance, emotions, and motor function based on NIH toolbox
Changes in cognitive performance, emotions, and motor function in raw scores measured by the NIH Toolbox® (reports will be generated as T scores, with higher T scores indicating better outcomes)
At baseline and at 4 weeks after the corresponding training program.
Changes in executive function using the Behavior Rating Inventory of Executive Function-Adult Version (BRIEF-A)
Changes in executive function using the Behavior Rating Inventory of Executive Function-Adult Version (BRIEF-A) (reports will be generated as T scores, with lower T scores indicating better outcomes and T scores higher than 65 indicating significant impairments in the executive function)
At baseline and at 4 weeks after the corresponding training program.
Changes in Blood Bioenergetic Markers
Platelet mitochondrial respiration (OCR) and extracellular acidification rates (ECAR) will be evaluated to assess bioenergetic profiles in platelets isolated from whole blood of fasted participants. OCR will be measured using a Seahorse model XFe96 machine as the high throughput platform. Measurements of OCR/ECAR will be performed with the following modifications. Platelets will be isolated from whole blood with a Beckman Allegra model X-30R centrifuge. Platelets will be counted using a Nexcelom Bioscience Cellometer (Lawrence, MA) using Calcein acetoxymethyl (AM) ester dye to enable the seeding of 10,000,000 platelets per well.
At baseline and at 4 weeks after the corresponding training program.
Nebenergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
VO2peak
VO2peak will be used as the primary measure of aerobic capacity. Subjects will be asked to exercise to voluntary exhaustion during a treadmill test using a modified Bruce protocol. Oxygen (O2) consumption, carbon dioxide (CO2) production, and minute ventilation will be measured breath-by-breath using a metabolic cart and the average of the final two 20 second values of O2 consumption are VO2peak.
At baseline and within one week after the corresponding training program.
Eignungskriterien

Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
50 Years
Zugelassene Geschlechter
Alle
Akzeptiert gesunde Freiwillige
Ja
  • Adult men and women of all races and ethnicities who are 50-80 years of age will be eligible.
  • Only sedentary adults will be eligible (engaging in structured activity for exercise <3x/week) for Progressive aerobic exercise or Combined training
  • Ability to use, and accessibility to, an iPad or computer is required for the Adaptive cognitive training and Combined training.
  • Fluent in English.
  • The diagnosis of MCI will first be confirmed at the screening evaluation using the clinical dementia rating (CDR) scale and the Montreal Cognitive Assessment (MoCA). We will also evaluate their ADL using instrumental activities of daily living (IADL) to ensure they have preserved independence in functional abilities despite the cognitive deficits. The primary caregivers will be interviewed (either in person or by phone) for the participants' IADL to corroborate the independent functional status.

  • Does not have access to a computer or internet to perform the Cogmed® training AND is unwilling to come to the lab for the training.
  • Unable to undergo an MRI investigation based on claustrophobia or metal foreign bodies.
  • Symptomatic heart disease, Coronary artery disease, congestive heart failure, uncontrolled hypertension, uncontrolled diabetes (HbA1c>10%), significant cardiovascular disorders (on EKG and graded exercise test) that would prevent the participant from the exercise training; neurologic, musculoskeletal, or other condition that limits the subject's ability to complete study physical assessments.
  • Estimated verbal Intelligence Quotient (IQ) below 70 (based on the Wechsler Test of Adult Reading) which would invalidate the informed consent process for the study.
  • Self-reported moderate to severe substance use disorder(s) (e.g., self-reported intake >3 oz liquor, or three 4 oz glasses of wine, or three 12 oz cans of beer per day or illicit drug use).
  • Severe chronic or acute medical or other (non-MCI) neuropsychiatric conditions that might confound the cognitive or brain imaging measures (e.g., liver function tests >2.5 normal range or evidence for renal failure).
  • Body mass index >40 kg/m2.
University of Maryland, Baltimore logoUniversität von Maryland, Baltimore200 aktive klinische Studien zum Erkunden
Verantwortliche Partei
Linda Chang, Hauptprüfer, Principal Investigator, University of Maryland, Baltimore
Zentrale Studienkontakte
Kontakt: Linda Chang, M.D., M.S., 410 706 1036, [email protected]
1 Studienstandorte in 1 Ländern

Maryland

University of Maryland Baltimore, Baltimore, Maryland, 21201, United States
Huajun Liang, MBBS, PhD, Kontakt, 410-706-1031, [email protected]
Offene Rekrutierung