Clinical Time and Temporal Dynamics Study (CLIN-TIME) (CLIN-TIME)
Prospective Evaluation of Temporal Clinical Dynamics, Physiologic Trajectories, and Time-Dependent Digital Biomarkers for Prediction of Clinically Meaningful Patient Outcomes
Studieoversigt
Status
Status
Betingelser
Betingelser
- Biomarkører
- Telemedicin
- Forudsigende værdi af tests
- Kliniske resultater
- Pandemi
- Dødens tid
- Misbrugsstoffer
- Epidemisk sygdom
- Sexadfærd
- Fremtidsstudier
- Tidsopfattelse
- Befolkning
- Sundhedsrisici
- Kirurgisk
- Cardio-pulmonary
- Population Groups
- Kønshormon
- Kønskarakteristika
- Tidsstyring
- Tidseffektivitet
- Tidsreaktion
- Longitudinal Studies
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Kontakter og lokationer
Studiesteder
-
-
New York
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New York, New York, Forenede Stater, 10016
- Truway Health, Inc.
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Antal grupper/kohorter
Kohorter og interventioner
Gruppe / kohorteGruppe / kohorte |
Intervention / BehandlingIntervention / Behandling |
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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.
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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.
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Time-Dependent Predictive Discrimination of Clinically Meaningful Patient Outcomes
Tidsramme: At baseline and at 30 days, 90 days, 6 months, and 12 months after enrollment.
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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.
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At baseline and at 30 days, 90 days, 6 months, and 12 months after enrollment.
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Within-Participant Temporal Trajectory Variability
Tidsramme: At 30 days, 90 days, 6 months, and 12 months after enrollment.
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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.
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At 30 days, 90 days, 6 months, and 12 months after enrollment.
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Clinical Lead-Time to Prespecified Outcome
Tidsramme: From baseline through 12 months after enrollment.
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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.
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From baseline through 12 months after enrollment.
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Calibration of Time-Dependent Clinical Prediction Models
Tidsramme: At 30 days, 90 days, 6 months, and 12 months after enrollment.
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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.
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At 30 days, 90 days, 6 months, and 12 months after enrollment.
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Temporal Phenotype Stability
Tidsramme: At 90 days, 6 months, and 12 months after enrollment.
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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.
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At 90 days, 6 months, and 12 months after enrollment.
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Efterforskere
Efterforskere
- Ledende efterforsker: Gavin C Solomon, MD, Truway Health, Inc.
Publikationer og nyttige links
Generelle publikationer
- Badawy R, Hameed F, Bataille L, Little MA, Claes K, Saria S, Cedarbaum JM, Stephenson D, Neville J, Maetzler W, Espay AJ, Bloem BR, Simuni T, Karlin DR. Metadata Concepts for Advancing the Use of Digital Health Technologies in Clinical Research. Digit Biomark. 2019 Oct 7;3(3):116-132. doi: 10.1159/000502951. eCollection 2019 Sep-Dec.
- Chodankar D, Raval TK, Jeyaraj J. The role of remote data capture, wearables, and digital biomarkers in decentralized clinical trials. Perspect Clin Res. 2024 Jan-Mar;15(1):38-41. doi: 10.4103/picr.picr_219_22. Epub 2023 Oct 13.
- Holler E, Chekani F, Ai J, Meng W, Khandker RK, Ben Miled Z, Owora A, Dexter P, Campbell N, Solid C, Boustani M. Development and Temporal Validation of an Electronic Medical Record-Based Insomnia Prediction Model Using Data from a Statewide Health Information Exchange. J Clin Med. 2023 May 5;12(9):3286. doi: 10.3390/jcm12093286.
- Carrasco-Ribelles LA, Llanes-Jurado J, Gallego-Moll C, Cabrera-Bean M, Monteagudo-Zaragoza M, Violan C, Zabaleta-Del-Olmo E. Prediction models using artificial intelligence and longitudinal data from electronic health records: a systematic methodological review. J Am Med Inform Assoc. 2023 Nov 17;30(12):2072-2082. doi: 10.1093/jamia/ocad168.
- Pungitore S, Subbian V. Assessment of Prediction Tasks and Time Window Selection in Temporal Modeling of Electronic Health Record Data: a Systematic Review. J Healthc Inform Res. 2023 Aug 14;7(3):313-331. doi: 10.1007/s41666-023-00143-4. eCollection 2023 Sep.
- Bull LM, Lunt M, Martin GP, Hyrich K, Sergeant JC. Harnessing repeated measurements of predictor variables for clinical risk prediction: a review of existing methods. Diagn Progn Res. 2020 Jul 9;4:9. doi: 10.1186/s41512-020-00078-z. eCollection 2020.
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
- Digital sundhed
- Fjernovervågning
- Forudsigende analyse
- Dynamisk risikoforudsigelse
- Longitudinal Monitoring
- Clinical Temporal Dynamics
- Clinical Time
- Temporal Biomarkers
- Longitudinal Clinical Data
- Physiologic Trajectories
- Temporal Phenotyping
- Clinical Trajectory
- Individualized Baseline
- Physiologic Velocity
- Physiologic Acceleration
- Recovery Kinetics
- Temporal Digital Biomarkers
- Clinical Surveillance
- Time-Dependent Outcomes
- Long-Term Clinical Outcomes
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- TH-CLINICAL-TIME-2026-001
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
- CSR
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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