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Clinical Time and Temporal Dynamics Study (CLIN-TIME) (CLIN-TIME)

4 septembre 2026 mis à jour par: Truway Health, Inc.

Prospective Evaluation of Temporal Clinical Dynamics, Physiologic Trajectories, and Time-Dependent Digital Biomarkers for Prediction of Clinically Meaningful Patient Outcomes

TH-CLINICAL-TIME is a prospective, longitudinal observational study evaluating how changes in clinical measurements over time may help researchers better understand patient health trajectories and clinically meaningful outcomes. The study will examine patterns such as changes from an individual's baseline, rate of change, persistence of abnormalities, variability, recurrence, and recovery following clinical events. Data may include routinely collected clinical measurements, physiologic observations, laboratory results, cardiac measurements, imaging-derived measurements, patient-reported information, and remote or digital health data when available and permitted by the study protocol. The study will investigate whether these temporal patterns provide additional information beyond individual measurements taken at a single point in time. The planned study horizon extends from 2026 through 2076, while individual participant follow-up will occur according to the approved study schedule, consent, and applicable requirements.

Aperçu de l'étude

Description détaillée

TH-CLINICAL-TIME is a prospective longitudinal observational research study designed to investigate the role of temporal dynamics in clinical medicine. The fundamental premise is that a clinical measurement may have different significance depending on its relationship to a patient's prior measurements, the direction and rate of change, the duration of an observed abnormality, the sequence of preceding or subsequent observations, and the patient's subsequent recovery or deterioration.

The study will establish longitudinal research datasets that permit evaluation of individual and population-level clinical trajectories. Depending on the participating cohort and available clinical data, observations may include vital signs, physiologic measurements, electrocardiographic information, cardiovascular measurements, point-of-care ultrasound or other imaging-derived measurements, laboratory results, symptoms, medications, procedures, healthcare encounters, patient-reported outcomes, and appropriately governed remote or digital health measurements.

A principal research objective is to determine whether time-dependent clinical features provide incremental information beyond conventional point-in-time measurements. Investigational temporal features may include baseline deviation, velocity of change, acceleration or deceleration, persistence, variability, recurrence, temporal sequence, time between clinically relevant observations, and recovery kinetics.

The study will investigate the concept of an individualized Clinical Temporal Phenotype, representing the longitudinal behavior of selected clinical variables rather than a single measurement. Individualized analyses may compare a participant's current observations with their own longitudinal baseline as well as with appropriate population reference distributions.

The research program may evaluate whether temporal patterns are associated with predefined clinical outcomes, including clinically meaningful deterioration, hospitalization, emergency evaluation, cardiovascular events, procedure-related outcomes, recovery characteristics, readmission, or other protocol-defined outcomes. Specific endpoints, populations, data sources, analytic methods, and follow-up schedules will be prespecified in the applicable study protocol and statistical analysis plan.

Where appropriate, longitudinal statistical and computational methods may be used to evaluate trajectories and dynamic prediction. These may include longitudinal regression, survival analysis, time-dependent modeling, recurrent-event analysis, joint longitudinal-survival models, dynamic risk prediction, and machine-learning methods. Any predictive models will be evaluated using appropriate temporal validation methods designed to prevent incorporation of future information into predictions of earlier events.

An additional research objective is to evaluate clinical lead time, defined as the interval between identification of a prespecified research signal and a subsequently documented clinical event or clinical recognition point. Research analyses may also evaluate whether recovery kinetics, recurrent deviations, or accelerating changes contain prognostic information.

Remote and digital data may be incorporated when specifically permitted by the study protocol, participant authorization, applicable privacy requirements, and institutional policies. Research-generated alerts or analytical signals will not independently constitute clinical diagnoses or treatment recommendations unless a separately authorized clinical-care process exists.

The study has a planned 50-year study-level horizon from 2026 through 2076 to permit investigation of long-term longitudinal patterns. The study horizon does not imply that every participant will be followed continuously for 50 years. Individual participation and follow-up duration will be governed by the approved protocol, informed consent or other applicable authorization, participant withdrawal, availability of follow-up data, and applicable institutional and regulatory requirements.

The study will employ coded research identifiers and appropriate data-governance procedures. Direct participant identifiers will be maintained separately from research datasets to the extent required by the applicable protocol and institutional policies. Research data will be subject to appropriate access controls, auditability, security safeguards, quality-control procedures, and retention and disposition requirements.

The study is observational and does not, by itself, assign participants to an experimental drug, biologic, or device intervention. Any clinical care received by participants remains under the direction of their treating healthcare professionals and is not altered solely by participation in the observational research unless separately specified in an approved protocol.

The overarching scientific objective is to determine whether clinical time itself can be characterized as a measurable dimension of patient state, and whether longitudinal trajectories, rather than isolated observations, can yield reproducible research biomarkers of clinical change, deterioration, and recovery.

Type d'étude

Observationnel

Inscription (Estimé)

1000

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

    • New York
      • New York, New York, États-Unis, 10016
        • Truway Health, Inc.

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

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

The study population will consist of adults aged 18 years and older, including individuals with and without established medical conditions. Participants will be followed longitudinally to characterize individualized clinical trajectories and temporal dynamics using available clinical, physiologic, laboratory, imaging-derived, patient-reported, and remote or digital health information as permitted by the protocol. The population is intended to support evaluation of temporal biomarkers, longitudinal patterns, clinical trajectory features, and time-dependent associations with clinically meaningful outcomes.

La description

Inclusion Criteria:

  • Adults aged 18 years or older.
  • Able and willing to provide informed consent, when informed consent is required by the approved study protocol and applicable regulations.
  • Willing and able to participate in longitudinal collection or evaluation of clinical, physiologic, laboratory, imaging-derived, patient-reported, or remote/digital health information as applicable to the study protocol.
  • Ability to complete the protocol-defined follow-up schedule or provide sufficient longitudinal observations for analysis.
  • Individuals with or without established medical conditions may be eligible, provided their participation is consistent with the study protocol.
  • Availability of sufficient baseline information or measurements to establish an individualized reference state when required for the applicable analysis.

Exclusion Criteria:

  • Inability to provide informed consent when consent is required and no legally authorized representative process is applicable.
  • Inability to comply with protocol-defined data collection or follow-up requirements.
  • Circumstances that, in the judgment of the investigator, would prevent reliable longitudinal data collection or interpretation.
  • Enrollment in another research protocol that would materially interfere with participation or interpretation of the outcomes, when applicable.
  • Any other exclusion criterion specifically identified in the IRB/ethics-approved protocol.

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

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
Clinical Time Longitudinal Cohort
Participants enrolled in this prospective observational cohort will be followed longitudinally according to the approved study schedule. The cohort will be evaluated for temporal clinical dynamics, including changes from individualized baseline, rate and acceleration of change, persistence, variability, recurrence, temporal sequence, and recovery following clinically meaningful events. Analyses will integrate available longitudinal clinical, physiologic, laboratory, imaging-derived, patient-reported, and remote or digital health measurements when permitted by the study protocol. No experimental intervention is assigned by the study.
This is a prospective observational study with no protocol-assigned drug, biologic, device, behavioral intervention, or other therapeutic intervention. Participants receive clinical care according to usual practice and applicable clinical decisions. The study observes and analyzes longitudinal clinical and physiologic data to characterize temporal dynamics and their association with clinically meaningful outcomes. Data collection may include routinely available clinical measurements, laboratory results, imaging-derived measurements, patient-reported information, and remote or digital health measurements when permitted by the protocol.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Time-Dependent Predictive Discrimination of Clinically Meaningful Patient Outcomes
Délai: At baseline and at 30 days, 90 days, 6 months, and 12 months after enrollment.
Change in predictive discrimination of longitudinal temporal clinical features compared with point-in-time clinical measurements for prespecified clinically meaningful patient outcomes. Predictive discrimination will be quantified using the prespecified time-dependent area under the receiver operating characteristic curve (AUC) or concordance index (C-index), as applicable to the outcome and statistical analysis plan. Temporal features will include individualized baseline values and longitudinal rates of change.
At baseline and at 30 days, 90 days, 6 months, and 12 months after enrollment.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Within-Participant Temporal Trajectory Variability
Délai: At 30 days, 90 days, 6 months, and 12 months after enrollment.
Quantification of within-participant longitudinal variability in prespecified physiologic and clinical measurements using the coefficient of variation calculated from repeated assessments. The analysis will characterize individualized temporal trajectories while preserving participant-level longitudinal structure.
At 30 days, 90 days, 6 months, and 12 months after enrollment.
Clinical Lead-Time to Prespecified Outcome
Délai: From baseline through 12 months after enrollment.
Time in days between the first prespecified temporal signal meeting the protocol-defined detection threshold and the subsequent occurrence or clinical recognition of the corresponding prespecified clinically meaningful outcome. Lead-time will be calculated only for participants experiencing the applicable outcome during observation.
From baseline through 12 months after enrollment.
Calibration of Time-Dependent Clinical Prediction Models
Délai: At 30 days, 90 days, 6 months, and 12 months after enrollment.
Calibration of prespecified longitudinal clinical prediction models for clinically meaningful patient outcomes, assessed by the calibration slope and calibration-in-the-large at each scheduled assessment point. Model calibration will be evaluated according to the prespecified statistical analysis plan.
At 30 days, 90 days, 6 months, and 12 months after enrollment.
Temporal Phenotype Stability
Délai: At 90 days, 6 months, and 12 months after enrollment.
Proportion of participants whose prespecified individualized temporal phenotype classification remains concordant across consecutive scheduled longitudinal assessments. Stability will be determined using the protocol-defined phenotype classification algorithm.
At 90 days, 6 months, and 12 months after enrollment.

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Chercheur principal: Gavin C Solomon, MD, Truway Health, Inc.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

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)

1 septembre 2026

Achèvement primaire (Estimé)

1 septembre 2076

Achèvement de l'étude (Estimé)

1 septembre 2076

Dates d'inscription aux études

Première soumission

1 septembre 2026

Première soumission répondant aux critères de contrôle qualité

4 septembre 2026

Première publication (Réel)

10 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

10 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

4 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

Individual participant-level data (IPD) will be considered for sharing with qualified researchers following publication of the primary study results, subject to applicable informed consent, institutional policies, privacy requirements, data-use agreements, and regulatory requirements. Shared datasets will be de-identified or appropriately anonymized and will exclude direct participant identifiers. Requests will be evaluated based on scientific merit, data availability, participant privacy, and compatibility with the study consent and governance framework. Data may be provided through a controlled-access process rather than unrestricted public release.

Délai de partage IPD

Individual participant-level data (IPD) and supporting information will become available after publication of the primary study results and completion of data-quality, privacy, and governance review. Data will be available beginning at that time for qualified research purposes through a controlled-access process. The study protocol, statistical analysis plan, clinical study report, and analytic code will be made available when finalized and permitted by applicable policies and agreements. Access will continue for as long as the data and supporting materials remain available and appropriate for controlled research use, subject to applicable privacy, consent, regulatory, and institutional requirements.

Critères d'accès au partage IPD

De-identified individual participant-level data and applicable supporting information may be requested by qualified researchers for scientifically valid research purposes. Requests will be reviewed by the designated study research governance authority for scientific merit, feasibility, data availability, participant privacy, consistency with informed consent, and applicable regulatory and institutional requirements. Approved researchers will be required to execute an appropriate data-use agreement and comply with confidentiality, security, and permitted-use restrictions. Data will be provided through a controlled-access mechanism; direct participant identifiers will not be provided. Supporting materials may include the study protocol, statistical analysis plan, clinical study report, and analytic code, as available and permitted.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE
  • ANALYTIC_CODE
  • RSE

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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