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Fitness pour aider le cerveau et les compétences cognitives (Fit ABCS)

21 septembre 2026 mis à jour par: Donald Mabbott, The Hospital for Sick Children

Développement d'un programme d'entraînement physique basé sur le Web pour la réparation du cerveau et la récupération cognitive pour les survivants de tumeurs cérébrales pédiatriques dans la communauté : une étude de faisabilité

The study will assess the feasibility of a pilot clinical trial of community-led aerobic exercise training for paediatric brain tumour survivors (PBTS) and the feasibility of a web-based platform to deliver this exercise training. It is hypothesized that 12 weeks of community-led exercise training will be feasible for PBTS and the web-based platform will be feasible to deliver exercise training by community-based instructors.

Aperçu de l'étude

Description détaillée

PBTS will complete 12 consecutive weeks of exercise training. Exercise training will involve 90-minute group sessions of aerobic activity 3 times/week with a 30-minute snack/reward time. The investigators anticipate participants will complete the exercise training program in cohorts, each comprised of a minimum of 3 and maximum of 10 participants. With a minimum of 3 participants per cohort, in order for us to achieve the investigators' goal of recruiting 30 participants, the investigators anticipate running approximately 7 cohorts. Participants will be assigned to a cohort based on proximity to session location and availability to attend sessions.

Site Description:

This is a single-site trial, as participants will be recruited from SickKids. Community-led exercise training will be delivered at various locations across the Greater Toronto and Hamilton Area (GTHA). Exercise training sessions will be conducted in partnership with Wellspring, a network of community support services across the GTHA for individuals diagnosed and treated for cancer. The investigators have developed a web-based platform for Fitness Trainers/Therapists (FTTs) to i) educate them on working with PBTS, ii) build exercise session plans, and iii) provide feedback on sessions and overall web-based platform functionality and usability. The web-based platform will allow the administration of community-led exercise training in any location. To test the feasibility of the web-based platform, the investigators will be administering exercise training in approximately 5 locations associated with Wellspring centres (and/or surrounding gymnasiums or outdoor space) and Wellspring FTTs.

Study Intervention Description:

Exercise training will consist of group sessions of aerobic exercise. Each session will include five (5) components:

  1. Warm-up activities
  2. Aerobic training activities
  3. Group sports/games
  4. Cool-down activities
  5. Snack/reward time The goal of the intervention is to increase and maintain participants' heart rate for at least 30 minutes per session at a minimum of 80% of participants' peak heart rate achieved during a baseline fitness assessment. Increased heart rate will mainly take place during the aerobic circuit training and group sport/game components of each session. Heart rate will be measured using heart rate monitors.

Description of study population:

  • Sample size: n = 40 (30 PBTS, 10 Healthy Controls)
  • Age: 6-17 years
  • Sex: males and females
  • General health [PBTS]: Patients who have completed treatment for hemispheric or posterior fossa tumours and do not have severe neurological/motor dysfunction that would preclude safe participation in an exercise program
  • General health [Healthy Controls]: Do not have neurological/motor dysfunction that would preclude safe participation in baseline assessment or have a prior history of neurodevelopmental or neurological disorder, cerebral palsy, developmental delay or learning disability at time of enrollment
  • Geographic location: Canada

Type d'étude

Interventionnel

Inscription (Réel)

26

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Ontario
      • Toronto, Ontario, Canada, M5G 1X8
        • The Hospital for Sick Children

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

6 ans à 18 ans (Enfant, Adulte)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Between 6 years and 17 years and 11 months of age at time of enrollment
  2. Diagnosed with a brain tumour
  3. 1 to 15 years between diagnosis and time of study enrollment
  4. Medically stable (i.e. must be in remission) as determined by a permanent SickKids staff Neuro-Oncologist
  5. Either declare English as their native language or have at least two years of schooling in English at the time of their first assessment
  6. Have a parent or legal guardian willing to complete the Health and Quality of Life measures
  7. Informed consent (and assent, where applicable) will be obtained from the participants and/or their legal guardians

Exclusion Criteria:

  1. Any condition or diagnosis, that could in the opinion of the Principal Investigator or delegate, interfere with the participant's ability to comply with study instructions, might confound the interpretation of the study results, or put the participant at risk
  2. Diagnosed with a neurodevelopmental or neurological disorder, cerebral palsy, developmental delay or learning disability prior to initial brain tumour diagnosis that would preclude safe participation
  3. Receiving palliative care
  4. Require sedation for neuroimaging
  5. Have ferrous metal implants (i.e. cochlear implant, braces, etc.)
  6. Have a programmable shunt
  7. Pregnant
  8. Completed any prior cognitive rehabilitation intervention within three months of enrollment

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: FitABCS exercise

Web-based community-led, 12-week exercise program

Community based FTTs will use a web-based platform to deliver a 12-week exercise training program (120-minute group sessions of aerobic activity 3 times/week). Each session will include:

  • Warm-up activities
  • Aerobic activities and fitness training in a game-like fashion
  • Organized sports/games
  • Cool down activity
  • Snack/reward time
Aucune intervention: FitABCS control

Healthy control

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Feasibility of the exercise program: The probability that 30 eligible patients will be recruited
Délai: 24 Months

In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory patient recruitment. The goal is to recruit n=30 participants (≥25% probability)

Measure: The Bayesian probability statistic that 30 eligible patients will be recruited

24 Months
Feasibility of the exercise program: The probability that a recruited participant will attend ≥60% of exercise training sessions
Délai: 24 weeks

In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory participant attendance. The goal is for a participant to attend ≥60% of exercise training sessions (≥80% probability of participants).

Measure: The Bayesian probability statistic that participants will rate the therapeutic alliance between participant/instructor as cooperative and collaborative.

24 weeks
Feasibility of the exercise program: The probability that a recruited participant will complete all study procedures
Délai: 24 weeks

In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory participant adherence to study procedures (neuroimaging, cognitive, health and quality of life (QOL), cardiovascular fitness and physical functioning assessments). The goal is for a recruited participant to complete all study procedures (≥80% probability).

Measure: The Bayesian probability statistic that a recruited participant will complete all study procedures

24 weeks
Feasibility of the exercise program: The probability that instructors will adhere to the web-based platform to deliver exercise training
Délai: 24 weeks

In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory instructor adherence to deliver the program. The goal is for instructors to adhere to the web-based platform to deliver exercise training (≥80% probability).

Measure: The Bayesian probability statistic that instructors will adhere to the web-based platform to deliver exercise training

24 weeks
Feasibility of the exercise program: The probability that instructors will develop a therapeutic alliance with the participants
Délai: 24 weeks

In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory rating by the participant of the therapeutic alliance between participants and instructors. The goal is for participants to have a cooperative and collaborative relationship with the instructors, as rated by the Therapeutic Alliance Scales for Children-Revised questionnaire.

Measure: The Bayesian probability statistic that the therapeutic alliance between participant/instructor will be comparable across cohorts.

24 weeks
Feasibility of the web-based platform: The probability that instructors will rate the platform as acceptable
Délai: 24 weeks

In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as acceptable (e.g. would recommend to others, would continue to use). The goal is for instructors to rate the the platform as acceptable, indicating ease of use and satisfaction (≥80% probability).

Measure: The Bayesian probability statistic that instructors will rate the platform as acceptable

24 weeks
Feasibility of the web-based platform: The probability that instructors will rate the platform as relevant
Délai: 24 weeks

In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as relevant (e.g. includes all necessary components to administer an exercise program, would choose to use such a tool to deliver an exercise program).The goal is for the instructors to rate the platform as relevant, indicating the presence of necessary information (≥80% probability).

Measure: The Bayesian probability statistic that instructors will rate the platform as relevant

24 weeks
Feasibility of the web-based platform: The probability that instructors will rate the platform as efficient
Délai: 24 weeks

In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as efficient (e.g. is useful). The goal is for the instructors to rate the platform as efficient, indicating its usefulness (≥80% probability).

Measure: The Bayesian probability statistic that instructors will rate the platform as efficient

24 weeks

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Comparison of community-led vs. historical hospital-led exercise training program: Changes in hippocampal volume
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training for PBTS in terms of changes in hippocampal volume using MRI (magnetic resonance imaging).

Measures: Anatomical T1 weighted MRI will acquire estimates of hippocampal volume

Baseline, Week 13, and Week 25
Comparison of community-led vs. historical hospital-led exercise training program: Changes in neural communication
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training for PBTS in terms of changes in neural communication, as estimated by functional connectivity during magnetoencephalography (MEG) recording.

Measures: The weighted phase lag index (wPLI) will be used to measure functional connectivity during MEG recording as an estimate of neural communication

Baseline, Week 13, and Week 25
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in information processing speed
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in information processing speed.

Measure: Scores on the Rapid Visual Information Processing subtest of the Cambridge Neuropsychological Test Automated Battery

Baseline, Week 13, and Week 25
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in controlled attention
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in controlled attention.

Measure: Scores on the Match to Sample Visual Search Task subtest of the Cambridge Neuropsychological Test Automated Battery

Baseline, Week 13, and Week 25
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in declarative memory
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in declarative memory.

Measures: Scores on the Delayed Matching to Sample Task subtest of the Cambridge Neuropsychological Test Automated Battery

Baseline, Week 13, and Week 25
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in cardiovascular fitness (heart rate, and sub-maximal and maximal work rates)
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in cardiovascular fitness, including heart rate, sub-maximal and and maximal work rates.

Measures: 6-Minute Walk Test and electrically braked cycle ergometer to measure heart rate, and sub-maximal and maximal pro-rated work rates

Baseline, Week 13, and Week 25
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in physical functioning (bilateral coordination and balance, and running speed/agility and strength)
Délai: Baseline, Week 13, and Week 25

To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in physical functioning, including bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility).

Measure: Bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility) using the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition. Minimum points scored: 0, maximum points scored: 80; higher scores account for greater motor proficiency (better outcomes)

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in white matter microstructure
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in white matter microstructure using diffusion kurtosis imaging (DKI)

Measures: DKI will acquire kurtosis measures of water diffusion in the brain (mean, axial, radial kurtosis)

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in hippocampal volume
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes hippocampal volume using Anatomical T1 MRI

Measures: Hippocampal volume estimated using Anatomical T1 MRI

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in neural communication
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in neural communication as estimated by functional connectivity during MEG recording.

Measures: The wPLI will be used to measure functional connectivity during MEG recording as an estimate of neural communication

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in information processing speed
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in information processing speed.

Measures: Scores on the Pattern Comparison Processing Speed Test subtest of the National Institutes of Health Toolbox and Reaction Time Task subtest RTI subtest of the Cambridge Neuropsychological Test Automated Battery

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in controlled attention
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in controlled attention

Measures: Scores on the Flanker Inhibitory Control & Attention Task subtest of the National Institutes of Health Toolbox, and the Stop Signal Task, Rapid Visual Information Processing, and Match to Sample Visual Search subtests of the of the Cambridge Neuropsychological Test Automated Battery

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in declarative memory
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in declarative memory

Measures: Scores on the Children's Auditory Verbal and Learning Test-2 or Rey Auditory Verbal Learning Test (for participants who will be 18 years of age at the time of study completion) and Delayed Matching to Sample subtest of the Cambridge Neuropsychological Test Automated Battery

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in full scale intelligence
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in full scale intelligence.

Measures: Scores on the Vocabulary and Matrix Reasoning subtests of the Wechsler Abbreviated Scale of Intelligence-Second Edition

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in MEG behavioural measures
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in MEG behavioural measures.

Measures: Reaction time and accuracy scores on the Simple and Choice Visual-Motor Reaction Time Task, and Multi-Source Interference Task during MEG recording

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Health and QOL
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in health and QOL

Measure: Scores on the Patient-Reported Outcomes Measurement Information System - Global health 7+2, Pediatric Quality of Life Scale generic core scale, physical activity preference questionnaire and Habitual Physical Activity Scale. All health and QOL measures are parent-proxy reports.

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in cardiovascular fitness (heart rate, and sub-maximal and maximal work rates)
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in cardiovascular fitness, including heart rate, sub-maximal and and maximal work rates.

Measures: 6-Minute Walk Test and electrically braked cycle ergometer to measure heart rate, and sub-maximal and maximal pro-rated work rates

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in physical functioning (bilateral coordination and balance, and running speed/agility and strength, and ataxia)
Délai: Baseline, Week 13, and Week 25

To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in physical functioning, including bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility), and ataxia.

Measure: Bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility) using the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition. Minimum points scored: 0, maximum points scored: 80; higher scores account for greater motor proficiency (better outcomes), strength assessment conducted by a registered Physiotherapist and the Scale for the Assessment and Rating of Ataxia. Minimum points scored: 0, maximum points scored: 40; higher scores indicate increased severity of ataxia (worse outcome)

Baseline, Week 13, and Week 25
Impact of this study intervention on PBTS: Changes in physical functioning as reported by parent (PEDI-CAT)
Délai: week 25

To investigate the impact of community-let exercise training in PBTS to improve physical functioning in the participant's daily life, as reported by their parent.

Measure: Parent report the ease of physical (and cognitive) activities in their child's daily life.

week 25
Comparing brain structure outcomes before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in brain structure following exercise training and at 3-month follow up compared to before exercise training.

Measures: brain structure (MRI) as assessed through white matter microstructure as estimated by kurtosis (mean, axial, and radial).

Baseline
Comparing brain function outcomes before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in brain function following exercise training and at 3-month follow up compared to before exercise training.

Measures: Hippocampal volume and functional connectivity (MEG) as estimated by the weighted Phase Lag Index (wPLI)

Baseline
Comparing cognitive outcomes (information processing speed) before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in cognition following exercise training and at 3-month follow up compared to before exercise training

Measures: Pattern Comparison Processing Speed Test, Reaction Time (RTI) (reaction time for simple and 5-choice conditions= measured in milliseconds, shorter reaction time is better)

Baseline
Comparing cognitive outcomes (controlled attention) before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in cognition following exercise training and at 3-month follow up compared to before exercise training

Measures: Flanker Inhibitory Control & attention Task, SST, RVP, and MTS)

SST: Stop Signal Task (stop signal reaction time = milliseconds, lower is better)

RVP: Rapid Visual information Processing (A prime = range 0-1, higher is better)

MTS: Match To Sample visual search (correct trials (all trials) = %, higher is better)

Baseline
Comparing cognitive outcomes (declarative memory) before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in cognition following exercise training and at 3-month follow up compared to before exercise training

Measures: CAVLT-2 or RAVLT, DMS

CAVLT-2: Children's Auditory Verbal Learning Test 2 (standard scores range from <60 to >140, higher is better)

RAVLT: Rey Auditory Verbal Learning Test (T scores range from < 20 to >80, higher is better)

DMS: Delayed Matching to Sample (correct trials (all trials) = %, higher is better)

Baseline
Comparing cognitive outcomes (full scale intelligence quotient) before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in cognition following exercise training and at 3-month follow up compared to before exercise training

Measures: 2 subtests (Vocabulary, Matrix Reasoning) where T-scores are computed (20-80 range) with a higher value denoting a better score.

Baseline
Comparing cognitive outcomes (MEG behavioral measures) before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in cognition following exercise training and at 3-month follow up compared to before exercise training

Measures: Go/No-Go task, MSIT

MSIT: Multi Source Interference Task (reaction time= milliseconds, lower is better; accuracy = /1, higher is better; this also applies to Go/No-Go)

Baseline
Comparing health outcomes before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in health and quality of life following exercise training and at 3-month follow- up compared to before exercise training.

Measure: PROMIS parent proxy scale- Global health 7+2, PedsQL generic core parent-proxy report

PROMIS: Patient-Reported Outcomes Measurement Information System (T-scores range 14.7-68.78, higher is better)

PedsQL: Pediatric Quality of Life scale (range 0-100, higher score is better QoL)

Baseline
Comparing quality of life outcomes before and after community-based exercise training to a group of healthy age-matched peers
Délai: Baseline

To investigate whether PBTS participants more closely resemble their healthy peers in health and quality of life following exercise training and at 3-month follow- up compared to before exercise training.

Measure: HAES parent-proxy report, and PEDI-CAT

HAES: Habitual Activity Estimation Scale (active hours = higher is better, inactive hours= lower is better)

PEDI-CAT: pediatric evaluation of disability inventory computer adaptive test (scaled scores range 20-80, higher is better)

Baseline

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Donald J Mabbott, The Hospital for Sick Children

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

7 octobre 2021

Achèvement primaire (Réel)

11 mars 2025

Achèvement de l'étude (Réel)

11 mars 2025

Dates d'inscription aux études

Première soumission

22 avril 2022

Première soumission répondant aux critères de contrôle qualité

4 mai 2022

Première publication (Réel)

10 mai 2022

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

24 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

21 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 1000073462

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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