Telerehabilitation in Alzheimer's Disease (VRTAD)
30. juli 2026 oppdatert av: Sandro Iannaccone, IRCCS San Raffaele
Home-based Virtual Reality Cognitive Training as an add-on to Telerehabilitation in Alzheimer's Disease: Validation of a Protocol to Slow Down Cognitive Decline and Reduce Caregivers' Burden
Telemedicine has developed rapidly during the COVID-19 pandemic and is now integrated into the clinical practice of many hospitals. Telemedicine offers many advantages, and even after the end of the pandemic, many patients still choose to undergo healthcare visits remotely. However, the rapid expansion of telemedicine may be associated with the risk of providing patients with unvalidated and uncontrolled telehealth solutions, potentially negatively impacting their health.
In this study, the researchers aim to investigate the effectiveness of remote cognitive training in patients with mild-to-moderate Alzheimer's disease (AD) using tablets equipped with virtual reality-based cognitive exercises. The investigators also aim to evaluate the impact of online supervision of cognitive training by a neuropsychologist and to compare the costs and burden of home-based versus hospital-based cognitive training in patients with AD. This project will define the optimal modalities for cognitive telerehabilitation to ensure validated protocols for the continuity of care in AD.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
This project aims to use new technologies and telemedicine to ensure continuity of care and slow cognitive decline in patients with Alzheimer's disease (AD). The investigators also aim to reduce caregiver burden and healthcare costs for the national healthcare system.
The investigators hypothesize that patients provided with a VRRS tablet and undergoing autonomous cognitive training as an adjunct to cognitive telerehabilitation will achieve better cognitive outcomes than patients who do not receive a VRRS tablet.
The investigators also hypothesize that patients receiving both forms of cognitive training-autonomous training using the VRRS tablet combined with online cognitive telerehabilitation supervised by a professional neuropsychologist-will show greater improvements in cognitive function than patients who do not receive online cognitive telerehabilitation.
This is a prospective, interventional, randomized, single-blind, monocentric clinical study.
Study population: 48 patients with AD (MMSE score 18-24) and one caregiver for each patient (48 caregivers in total).
To minimize potential bias, the neuropsychologist responsible for patient and caregiver assessments will be blinded to treatment allocation.
Patients will be randomized in a 1:1:1 ratio to one of the following treatment groups:
- Intervention Group 1:** 16 patients provided with a VRRS tablet to perform autonomous home-based cognitive training (5 days per week), in addition to online cognitive telerehabilitation sessions supervised by a neuropsychologist at San Raffaele Hospital twice weekly.
- Intervention Group 2:** 16 patients provided with a VRRS tablet to perform autonomous home-based cognitive training (5 days per week), without neuropsychologist-supervised cognitive telerehabilitation.
- Comparator Group 3:** 16 patients receiving online cognitive telerehabilitation sessions supervised by a neuropsychologist twice weekly. These patients will not receive a VRRS tablet for home use.
No interim analysis is planned.
Study design:
Each group will undergo a 3-month intervention according to the following schedule.
Group 1:
Autonomous home-based cognitive training using the VRRS tablet for 1 hour per day, 5 days per week.
Remote cognitive telerehabilitation sessions supervised by a neuropsychologist twice weekly.
Group 2:
Autonomous home-based cognitive training using the VRRS tablet for 1 hour per day, 5 days per week.
No cognitive telerehabilitation sessions.
Group 3:
Remote cognitive telerehabilitation sessions supervised by a neuropsychologist twice weekly.
No VRRS tablet and no additional autonomous home-based cognitive training.
- Study visits:
Patients and caregivers will attend the following visits:
- Enrolment.
- Screening (Day 1) and treatment initiation.
- Post-treatment assessment (after 3 months of treatment).
Follow-up assessment (3 months after completion of treatment).
- Methods of data collection
The following data will be collected:
- patients' neuropsychological performance;
- electroencephalographic (EEG) activity;
- caregivers' mental health and caregiver burden;
- system usability;
- costs associated with telerehabilitation and cognitive training.
- Assessment of patients' neuropsychological performance:
Patients will undergo a comprehensive neuropsychological assessment at three time points: baseline, after the 3-month treatment period, and at the 3-month follow-up.
The assessment battery will include:
- Montreal Cognitive Assessment (MoCA) (primary outcome): a screening tool for cognitive impairment providing a total score and six domain-specific index scores (Memory, Executive Function, Attention, Language, Visuospatial Ability, and Orientation). Total scores range from 0 to 30, with scores ≥26 generally considered normal.
- Mini-Mental State Examination (MMSE).
- Quality of Life in Alzheimer's Disease (QoL-AD).
- Geriatric Depression Scale (GDS).
- Attention Matrices.
- Raven's Progressive Matrices.
- Token Test.
- Semantic Fluency Test.
- Phonemic Fluency Test.
- Naming Test.
- Word-Picture Naming Test.
- Digit Span Test (forward and backward).
- Corsi Block-Tapping Test.
- Rey Complex Figure Test.
- Trail Making Test.
- EEG assessment:
Five minutes of resting-state EEG will be recorded using 32-channel EEG caps before and after the intervention to perform time-frequency analyses.
- Assessment of caregivers' mental health and burden:
- Beck Depression Inventory-II (BDI-II).
- Zarit Burden Interview.
Assessment of system usability:
System Usability Scale (SUS). Usability will be evaluated in terms of effectiveness, efficiency, and user satisfaction.
- Assessment of the costs of telerehabilitation and cognitive training:
The following cost components will be analysed:
- healthcare professional costs (neuropsychologist);
- outpatient clinic costs;
- telemedicine equipment costs for both patients and the hospital;
- patients' travel costs;
- cognitive training equipment costs;
- caregiver burden;
- system usability.
Any future research involving the collected data will require prior approval from the Ethics Committee (EC).
Studietype
Intervensjonell
Registrering (Antatt)
48
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Elise Houdayer, PhD
- Telefonnummer: +390226435739
- E-post: houdayer.elise@hsr.it
Studer Kontakt Backup
- Navn: Sandro Iannaccone, MD
- Telefonnummer: +390226435760
- E-post: iannaccone.sandro@hsr.it
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Ja
Beskrivelse
Inclusion criteria for patients with Alzheimer's disease (AD):
- Age between 50 and 90 years.
- Diagnosis of Alzheimer's disease according to established diagnostic criteria.
- Mini-Mental State Examination (MMSE) score between 18 and 24.
- Stable pharmacological treatment for at least 3 months before enrolment.
- Ability and willingness to provide written informed consent.
Inclusion criteria for caregivers:
- Age ≥18 years.
- Availability to assist the patient throughout the study.
- Ability and willingness to provide written informed consent.
Exclusion criteria for patients with Alzheimer's disease (AD):
- Refusal or inability to provide written informed consent.
- History of psychiatric disorders.
- Significant cerebrovascular disease.
- Severe visual or hearing impairment that could interfere with study procedures.
- Psychosis.
- Major depressive disorder.
- Alcohol or substance abuse.
- Use of psychotropic medications that may interfere with neuropsychological assessment or study treatment.
- Concurrent participation in another interventional pharmacological clinical trial.
- Any contraindication to undergoing EEG recording.
Exclusion criteria for caregivers:
- Refusal or inability to provide written informed consent.
- History of psychiatric disorders.
- Major depressive disorder.
- Alcohol or substance abuse.
- Use of psychotropic medications that may interfere with neuropsychological assessment.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Tablet + Telerehabilitation
Group 1: Participants will perform autonomous home-based cognitive training using a VRRS tablet (Khymeia Home Tablet) for 5 days per week, combined with online cognitive telerehabilitation sessions conducted twice weekly by a neuropsychologist based at San Raffaele Hospital (telemedicine sessions delivered remotely between the patient's home and the hospital).
The intervention will last 3 months.
|
Online sessions of cognitive telerehabilitation, twice a week, supervised by a neuropsychologist based at the San Raffaele hospital.
Patients equipped with VRRS tablets to undergo autonomous home-based cognitive training (5 days a week).
|
|
Eksperimentell: Tablet only
Group 2: Participants will perform autonomous home-based cognitive training using a VRRS tablet (Khymeia Home Tablet) for 5 days per week.
No cognitive telerehabilitation sessions supervised by a neuropsychologist will be provided.
The intervention will last 3 months.
|
Patients equipped with VRRS tablets to undergo autonomous home-based cognitive training (5 days a week).
|
|
Aktiv komparator: Telerehabilitation only
Group 3: Participants will receive online cognitive telerehabilitation sessions supervised by a neuropsychologist twice weekly (telemedicine sessions delivered remotely between the patient's home and the hospital).
Participants will not receive a VRRS tablet and will not perform additional autonomous home-based cognitive training.
|
Online sessions of cognitive telerehabilitation, twice a week, supervised by a neuropsychologist based at the San Raffaele hospital.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Montreal Cognitive Assessment (MoCA)
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
MoCA is a screening instrument to detect cognitive impairment.
It generates a total score and six domain-specific index scores: (1) Memory, (2) Executive Functioning, (3) Attention, (4) Language, (5) Visuospatial, and (6) Orientation.
The total possible score is 30 points; a score of 26 or above is considered normal, while scores below 26 may indicate cognitive impairment.
Increase in MoCA scores meaning improvement in cognitive functioning.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Telerehabilitation's costs
Tidsramme: At 3 months follow-up.
|
The total costs for 3 months of telerehabilitation will be evaluated. Costs related to the following elements will be summed up:
|
At 3 months follow-up.
|
|
Hospital-based cognitive training costs
Tidsramme: At 3 months follow-up.
|
The total costs for 3 months of cognitive rehabilitation in the outpatient clinic of the San Raffaele Hospital (Milan, Italy) will be evaluated. Costs related to the following elements will be summed up:
|
At 3 months follow-up.
|
|
Electroencephalographic (EEG) activity
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
Patients' electroencephalographic activity: 5 min of resting state EEG will be recorded using a 32 channel cap in order to perform time-frequency analyses before and after training.
EEG power in the alpha, beta and theta rangers will be analyzed.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Caregivers' mental status
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
- Beck Depression Inventory-II (BDI): 21-item self-report instrument assessing the common cognitive symptoms of depression.
BDI is considered a valid and reliable instrument for depression screening in the general population.
The BDI is scored by summing the highest ratings for each of the 21 items.
Each item is rated on a 4-point scale ranging from 0 to 3, and the total scores can range from 0 to 63. BDI total scores ranging from 0 to 13 represent "Minimal" depression; total scores from 14 to 19 represent "Mild" depression; total scores from 20 to 28 represent "Moderate" depression; and total scores from 29 to 63 represent "Severe" depression.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Caregivers' burden
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
Zarit Burden Interview: a standardized, 22-item assessment tool used by healthcare professionals to measure the subjective burden experienced by caregivers of individuals with chronic illnesses or dementia.
It evaluates the emotional, physical, social, and financial impacts of caregiving to identify individuals at risk for burnout.
It contains 22 questions rated on a 5-point scale (0 = Never, 1 = Rarely, 2 = Sometimes, 3 = Quite frequently, 4 = Nearly always).
The total score ranges from 0 to 88, with higher scores indicating greater perceived strain.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
System usability
Tidsramme: At the end of the 3-month rehabilitation period.
|
System Usability Scale (SUS): a reliable, 10-item questionnaire used in research to quickly measure the perceived usability of a product, software, or website.
Usability measurements consider different aspects: effectiveness (users can successfully achieve their goals), efficiency (how much effort and resources are spent to achieve those goals) and satisfaction (the experience was satisfactory).
Participants rate 10 statements (alternating positive and negative) on a 5-point scale (1 = Strongly Disagree, 5 = Strongly Agree), covering areas like ease of use, consistency, and complexity.
A SUS score does not represent a percentage.
Instead, scores are generally understood using standardized benchmarks and grading scales: (1) 80.3: Excellent (Grade A); (2) 71 - 80: Good (Grade B); (3) 68: Okay/Average; (4) 51 - 68: Poor (Grade C/D); (5) <51: Worst Imaginable (Grade F).
|
At the end of the 3-month rehabilitation period.
|
|
Mini Mental State Examination (MMSE)
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
The MMSE is a 30-point, 11-question screening tool used by clinicians to assess cognitive impairment.
It evaluates functions like memory, orientation, attention, language, and visuospatial skills, taking just 5 to 10 minutes to administer.
It is most commonly used to detect conditions like dementia or track cognitive decline over time.
The MMSE covers several key domains of mental ability to establish a comprehensive overview of a person's present cognitive performance: Orientation (10 points), registration (3 points), Attention and Calculation (5 points), Recall (3 points), Language and Visual Construction (9 points).
Scores are tallied out of 30, with higher scores indicating better cognitive function.
A score of 24 or higher is generally considered normal, while scores below that threshold suggest varying levels of cognitive impairment.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Quality of Live in Alzheimer's Disease (QoL-AD)
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
The QOL-AD is a 13-item questionnaire designed to assess-through both the patient and the caregiver-the quality of life (QOL) of patients diagnosed with Alzheimer's disease (AD).
The scale comprises 13 items measuring physical condition, mood, memory, functional abilities, interpersonal relationships, the ability to participate in meaningful activities, financial situation, and global assessments of self and overall QOL.
Items are rated on a four-point scale, with descriptors ranging from 1 (poor) to 4 (excellent).
Separate scores are calculated for patients and caregivers and then combined into a composite score (QoL-AD CS), in which patient ratings are weighted twice as heavily as caregiver ratings.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Geriatric Depression Scale (GDS)
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
The most widely used rating scale for assessing depressive symptoms in frail elderly patients and patients with dementia.
The scale consists of 15 binary-response questions (yes or no), each scored as 1 or 0. The final score ranges from 0 (no depressive symptoms) to 15 (probable presence of depression).
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Attention matrices
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
Attentional Matrices is a classic paper-and-pencil diagnostic tool primarily used to assess selective visual attention and visual scanning.
It requires patients to rapidly identify and cross out target numbers hidden among distractors within a strict time limit.
The test typically consists of three separate matrices containing rows and columns of random digits.
The patient is handed a sheet and given a brief timeframe (usually 45 seconds) to scan the matrix and cross out specific, pre-defined target numbers.
The task becomes progressively complex across the three matrices.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Raven's Progressive Matrices (RPM)
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
RPM are a widely used, non-verbal psychometric assessment designed to measure fluid intelligence, abstract reasoning, and problem-solving skills.
It evaluates an individual's ability to deduce relationships, identify patterns, and impose meaning on complex, abstract visual information.
Test-takers are presented with a series of visual matrices-typically 3 × 3 geometric patterns-with one piece missing.
The goal is to identify the underlying logical rule governing the pattern and select the correct missing piece from a set of multiple-choice options.
The test is "progressive" because the visual puzzles begin simply and become increasingly difficult, demanding more complex cognitive operations to solve as the test goes on.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Token test
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
The Token Test is a standardized neuropsychological assessment used to evaluate receptive language disorders (auditory comprehension).
It requires patients to follow increasingly complex spoken commands to manipulate small, colored plastic shapes (tokens).
During the assessment, 20 physical tokens-featuring combinations of two shapes (circles and squares), two sizes (large and small), and five colors (red, blue, green, yellow, and white)-are placed in front of the patient.
The test is typically divided into six sections of increasing difficulty: Simple commands: "Touch the red circle"; Complex/Two-part commands: "Touch the large green square and the small red circle"; Relational commands: "Touch the red circle with the blue sqaure".
While the original test by A widely used short version consists of 36 commands.
Points are awarded for correct manipulations.
Lower or cutoff scores (e.g., 25 or below on the 36-item version) indicate varying levels of receptive language impairments.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Semantic and phonemic fluency
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
emantic and phonemic fluency are critical neuropsychological tests evaluating language and executive functions like working memory, mental flexibility, and strategy generation.
Semantic fluency requires producing words within a specific category (e.g., animals), heavily relying on temporal lobe networks and semantic memory.
Phonemic fluency requires generating words starting with a specific letter (e.g., F, A, S), taxing frontal lobe executive systems and phonological knowledge.
The primary score is the sum of all valid, unique words generated within the 60-second limit.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Naming
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
Naming test evaluates an individual's ability to retrieve and articulate the names of visually presented objects or pictures.
It is primarily used to diagnose anomia (word-finding difficulty) and localize language impairments caused by stroke, traumatic brain injury, or neurodegenerative diseases like Alzheimer's.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Word-picture naming test
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
It is a core neuropsychological evaluation that asks a patient to verbally identify common objects, animals, or actions shown in pictures.
It is used to measure lexical retrieval (word finding), semantic memory, and speech fluency.
The examiner presents a series of line drawings or photographs one by one.
The patient is asked to state the name of the object as quickly and accurately as possible.
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
|
Digit Span test
Tidsramme: (1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
|
The Digit Span test is a core neuropsychological assessment of memory.
It features two parts: Digits Forward, which measures passive short-term verbal memory and attention by requiring verbatim repetition, and Digits Backward, which assesses executive working memory by demanding mental manipulation and sequence reversal.
Digits Forward: The examiner reads a random sequence of numbers aloud (e.g., "5-8-2-1") at a rate of one digit per second.
The participant must repeat the sequence in the exact same order.
Digits Backward: The examiner reads a sequence of numbers, and the participant must repeat the sequence in reverse order (e.g., if the examiner says "3-9-2", the correct response is "2-9-3").
|
(1) before telerehabilitation, (2) at the end of the 3-month rehabilitation period, and (3) 3 months following the end of treatment.
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
- Buschert V, Bokde AL, Hampel H. Cognitive intervention in Alzheimer disease. Nat Rev Neurol. 2010 Sep;6(9):508-17. doi: 10.1038/nrneurol.2010.113. Epub 2010 Aug 17.
- Laver KE, George S, Thomas S, Deutsch JE, Crotty M. Virtual reality for stroke rehabilitation. Cochrane Database Syst Rev. 2015 Feb 12;2015(2):CD008349. doi: 10.1002/14651858.CD008349.pub3.
- Gatica-Rojas V, Mendez-Rebolledo G. Virtual reality interface devices in the reorganization of neural networks in the brain of patients with neurological diseases. Neural Regen Res. 2014 Apr 15;9(8):888-96. doi: 10.4103/1673-5374.131612.
- Yang JG, Thapa N, Park HJ, Bae S, Park KW, Park JH, Park H. Virtual Reality and Exercise Training Enhance Brain, Cognitive, and Physical Health in Older Adults with Mild Cognitive Impairment. Int J Environ Res Public Health. 2022 Oct 15;19(20):13300. doi: 10.3390/ijerph192013300.
- Emedoli D, Houdayer E, Della Rosa PA, Zito A, Brugliera L, Cimino P, Padul JD, Tettamanti A, Iannaccone S, Alemanno F. Continuity of care for patients with dementia during COVID-19 pandemic: flexibility and integration between in-person and remote visits. Front Public Health. 2024 Jan 8;11:1301949. doi: 10.3389/fpubh.2023.1301949. eCollection 2023.
- Emedoli D, Alemanno F, Houdayer E, Brugliera L, Iannaccone S, Tettamanti A. Mobile application tool for remote rehabilitation after discharge from coronavirus disease-19 rehabilitation unit. Healthc Technol Lett. 2022 Aug 8;9(4-5):70-76. doi: 10.1049/htl2.12033. eCollection 2022 Aug-Oct.
- Elbaz S, Cinalioglu K, Sekhon K, Gruber J, Rigas C, Bodenstein K, Naghi K, Lavin P, Greenway KT, Vahia I, Rej S, Sekhon H. A Systematic Review of Telemedicine for Older Adults With Dementia During COVID-19: An Alternative to In-person Health Services? Front Neurol. 2021 Dec 14;12:761965. doi: 10.3389/fneur.2021.761965. eCollection 2021.
- Grabher BJ. Effects of Alzheimer Disease on Patients and Their Family. J Nucl Med Technol. 2018 Dec;46(4):335-340. doi: 10.2967/jnmt.118.218057. Epub 2018 Aug 23.
- Manenti R, Gobbi E, Baglio F, Macis A, Ferrari C, Pagnoni I, Rossetto F, Di Tella S, Alemanno F, Cimino V, Binetti G, Iannaccone S, Bramanti P, Cappa SF, Cotelli M. Effectiveness of an Innovative Cognitive Treatment and Telerehabilitation on Subjects With Mild Cognitive Impairment: A Multicenter, Randomized, Active-Controlled Study. Front Aging Neurosci. 2020 Nov 16;12:585988. doi: 10.3389/fnagi.2020.585988. eCollection 2020.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
1. oktober 2026
Primær fullføring (Antatt)
1. oktober 2029
Studiet fullført (Antatt)
1. oktober 2029
Datoer for studieregistrering
Først innsendt
3. juli 2026
Først innsendt som oppfylte QC-kriteriene
18. juli 2026
Først lagt ut (Faktiske)
23. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
3. august 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
30. juli 2026
Sist bekreftet
1. juli 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- RF-2024-12380126 VRTAD
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
IPD-planbeskrivelse
We do not plan to share IPD since this is a monocentric study, but all outcomes will be recorded and stored on a eCRF platform and will be be able to share data if requested by other researchers.
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .