Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Telehome Monitoring for Chronic Disease Management

12. Januar 2022 aktualisiert von: Claudia Baquet, University of Maryland, Baltimore

Effectiveness of Telehome Monitoring on Quality of Life and Health Resources Utilization Among People With Chronic Disease Residing in Rural Maryland

People living in rural areas are at increased risk for poor health outcomes due to: long distance to health care facilities, less available health care resources such as primary care and specialty services, transportation problems, higher elderly population, poverty, high uninsured rates and the lack of timely access to new technologies. Called Telehome Care (THC), in the form of equipment in the home, may provide an innovative and potentially cost-effective solution to enhancing chronic disease management services using technology and may influence the reduction in emergency department (ED) visits and hospitalizations in rural areas. However, telehealth research is still in its infancy, it is not well understood, and is often done without an overarching scientific framework. The provision of in home health monitoring and health education also may be a potential population based health research tool for chronically ill patients. Demonstration of the possible benefits, patient acceptance and satisfaction with THC requires a scientific approach as is used in this study.

Studienübersicht

Detaillierte Beschreibung

While the nation's overall health status has improved over the past decade, disparities persist among racial/ethnic minorities, low-income whites, the medically under-served, and rural residents. The disparities in disease morbidity and mortality are a compelling crisis and the elimination of such disparities is a national priority. With an aging population, the changing demographics are increasing the disease burden attributable to chronic diseases.

The broad goal of this project is to evaluate the potential value of using THC technology in chronically ill patients in rural Maryland, within the broad context of social determinants of health. This builds upon a completed pilot research study in Garrett County on a small scale THC program in rural Garrett County Maryland funded by the Maryland Cigarette Restitution Fund (CRF) supported Other Tobacco Related Diseases (OTRD grant) (CBaquet PI) in collaboration with the division of cardiology and department of family medicine. This research study will look at whether the THC equipment in the home for 60 days will make a difference in the health of the patients who get the unit in their home compared to the patients who will not receive the unit for 60 days. And we will look at whether this technology will support patient monitoring in the home. The use of the technology will be evaluated to determine whether patient monitoring using THC equipment will influence the hospitalization rates or emergency department visits for the patients. Evaluation of the influence of the THC equipment on medical resource utilization in rural and medically underserved communities will be studied.

Telehome care (THC) may provide augmentation to current face to face monitoring through home visits (usual method for Center for Medicaid and Medicare Services (CMS) billable home health services) of chronically ill patients and may provide an innovative and potentially cost-effective solution to improving patients' outcomes and health care resource utilization in rural areas. THC can support the coordination of care by assessing and monitoring patients in their homes and giving health care providers appropriate feedback to assure patient compliance with discharge instructions such as medication, home care and other aspects of recommended treatment regimens. Further, THC may improve service coordination at discharge and provide ongoing monitoring/engagement of patients, which is considered essential to prevent re-hospitalizations and emergency department visits. Demonstration of the potential benefits on care pathways, and patient and provider acceptance and satisfaction with the technology requires systematic larger scale and scientifically rigorous studies.

Purpose The project's broad goals are to evaluate the effects of telehome care (THC), a form of remote patient home monitoring,(within the broad context of social determinants of health) for chronic disease management among rural residing minority, low-income white, and medically underserved patients by: (a) providing an innovative telehome care (THC) capacity and infrastructure in two Maryland rural and medically underserved communities; and (b) using the THC infrastructure to generate scientifically rigorous and high quality evidence on whether the THC technology improves patient monitoring, influences clinical outcomes, and has an impact on medical resource utilization. [NOTE: THC uses telecommunication technologies to enable home health agency clinical staff at a rural home health agency to monitor their patients in the home.]

The major aim for this study are: 1) To evaluate the impact of the 60-day in home THC monitoring on medical resource utilization (emergency department visits; re-hospitalization rates) and Quality of Life related to the management of Metabolic Syndrome/Diabetes Mellitus (DM), Chronic Heart Failure (CHF), Hypertension (HTN), and Chronic Obstructive Pulmonary Disease (COPD) compared to those patients that receive only an educational pamphlet. Secondary aim hopes to support patient education to enhance acceptability, patient independence and satisfaction.

In this study, remote in-home patient monitoring using a THC system from VitelNet (telehealth equipment vendor) will provide patient monitoring remotely or non billable services for the experimental study arm for this project in addition to routine billable home health services. This project does not substitute billable in-home monitoring of patients which is a prerequisite for enrollment into this study(conventional home health services) but provides remote monitoring for the study arm in addition to conventional/billable services delivered.

Patients are randomized to either THC use for 60 days with 60, 90 day follow up or "usual care" with 60, 90 day follow up.

In addition, new knowledge will be generated by this study on methods for conduct of health disparities research and training of non-research clinical personnel who are community based in data collection and research ethics.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

23

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Maryland
      • Hughesville, Maryland, Vereinigte Staaten, 20637
        • Chesapeake-Potomac Home Health Agency
      • Oakland, Maryland, Vereinigte Staaten, 21550
        • Garrett County Health Department Home Health Agency

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

21 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Home bound at a home health agency (i.e., Garrett County Health Department Home Health Agency or Chesapeake-Potomac Home Health Agency)
  • Clinical diagnosis of at least one of the following: chronic obstructive pulmonary disease, chronic heart failure, uncontrolled hypertension, diabetes mellitus and taking anti-hyperglycemic oral therapy
  • Able to operate the telehome care system
  • Agreeable to have the telehome care system installed at residence for 60 days
  • Residing in an environment where care can be provided safely

Exclusion Criteria:

  • Not eligible for home health care
  • With a clinical diagnosis of a medical condition other than obstructive pulmonary disease, chronic heart failure, uncontrolled hypertension, diabetes mellitus and taking anti-hyperglycemic oral therapy
  • Unable to follow instructions about or be able to operate the telehome care system
  • Residing in an environment that is unsafe to provide home health care

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Unterstützende Pflege
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Kein Eingriff: Übliche Pflege
Experimental: Telehome Care Monitoring + Usual Care
Telehome care monitoring over a 60-day period wherein patients transmit health measurements to their health care professional on a daily basis

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Self reported Quality of life
Zeitfenster: The Outcome Measure(s) are assessing a change from Baseline and 90-day post-baseline
Assessing change from baseline to 90 day evaluated.
The Outcome Measure(s) are assessing a change from Baseline and 90-day post-baseline
Number of emergency department visits
Zeitfenster: The Outcome Measure(s) are assessing a change from Baseline and 90-day post-baseline

Assessing change from baseline to 90 day post baseline for:

  • exacerbation of a recent or remote diagnosis of chronic heart failure (post-baseline) requiring emergency department visit
  • exacerbation of chronic obstructive pulmonary disease (post-baseline) requiring emergency department visit
  • episodes of uncontrolled hypo/hyperglycemia (post-baseline) requiring emergency department visit
  • episodes of severe hypertension (post-baseline) requiring emergency department visit
The Outcome Measure(s) are assessing a change from Baseline and 90-day post-baseline
Re-hospitalization
Zeitfenster: Assessing change from baseline and 90-day post-baseline

Assessing change from baseline to 90 day post baseline for:

  • exacerbation of a recent or remote diagnosis of chronic heart failure (post-baseline) requiring hospital management
  • exacerbation of chronic obstructive pulmonary disease (post-baseline)requiring hospital management
  • episodes of uncontrolled hypo/hyperglycemia requiring emergency hospital management
  • episodes of severe hypertension requiring hospital management
Assessing change from baseline and 90-day post-baseline

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of contacts (visits or phone calls) with health care providers
Zeitfenster: Assessing change from baseline and 90-day post-baseline
Assessing change from baseline and 90-day post-baseline
Adequacy of hypertension control
Zeitfenster: Measures change from baseline and 90-day post-baseline
Measures change from baseline to 90 day post baseline for:adequacy of blood pressure control (<140/90 mmHg)
Measures change from baseline and 90-day post-baseline
Adequacy of diabetes control
Zeitfenster: Measures change from baseline and 90-day post-baseline
adequacy of glycemic control of HbA1C of <7.5
Measures change from baseline and 90-day post-baseline
Compliance with recommended (by discharging physician/primary health professional) drug therapy use for heart failure
Zeitfenster: Assessing change from baseline and 90-day post-baseline
Assessing change from baseline and 90-day post-baseline

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Claudia R Baquet, MD MPH, University of Maryland School of Medicine

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Februar 2011

Primärer Abschluss (Tatsächlich)

1. August 2012

Studienabschluss (Tatsächlich)

1. August 2012

Studienanmeldedaten

Zuerst eingereicht

16. Januar 2013

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

10. Januar 2014

Zuerst gepostet (Schätzen)

14. Januar 2014

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

27. Januar 2022

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

12. Januar 2022

Zuletzt verifiziert

1. Januar 2022

Mehr Informationen

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Klinische Studien zur Herzfehler

Klinische Studien zur Telehome Care Monitoring

3
Abonnieren