NCT00789100

Brief Summary

Nottingham Primary Care Trust has launched telemonitoring to support: independent living and self-management ability of people with congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD) and co-morbidities; and reduce the health care utilisation associated with these patients, including the number of hospitalisations, GP visits and community matron and specialist community nurse home visits. The Multidisciplinary Assessment of Technology Centre for Healthcare (MATCH) will evaluate the technology and its impact of this telemonitoring system on quality of care (i.e. process measures), patient outcomes and direct healthcare costs from an NHS perspective.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Feb 2009

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 10, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 11, 2008

Completed
3 months until next milestone

Study Start

First participant enrolled

February 1, 2009

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2010

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2011

Completed
Last Updated

July 17, 2014

Status Verified

July 1, 2014

Enrollment Period

1.5 years

First QC Date

November 10, 2008

Last Update Submit

July 15, 2014

Conditions

Keywords

telehealthtelemonitortelemedicineCo-morbidities

Outcome Measures

Primary Outcomes (1)

  • Hospitalizations, hospital days, encounters with health professionals

    Collected until end date

Study Arms (2)

1

Group provided with home-based monitor

2

Group receives no home-based monitor

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD) and co-morbidities referred to the community specialist nurse or care matron

You may qualify if:

  • Participants selected will be those: diagnosed with CHF, COPD or co-morbidities and referred to the community management service by its selection procedure for severity of the condition; are considered eligible for home-based telemonitoring; consent to receiving telemonitoring; have an active phone connection; are able to read and speak English (language of the equipment); are capable and willing to use the home monitoring device.

You may not qualify if:

  • Patients are considered ineligible: if they have psychological or psychiatric disorders; if they have a cognitive deficiency that makes them unable to participate in their self-treatment; if they have a visual or motor deficiency that renders them incapable of using the telemonitoring device (unless a spouse or an informal caregiver is able to help); if they are currently scheduled for a hospital admission; if their life expectancy is shorter than 2 years; or if they already participate in another study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nottingham PCT

Nottingham, Nottinghamshire, United Kingdom

Location

MeSH Terms

Conditions

Heart FailurePulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesLung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Malcolm Clarke, PhD

    Brunel University

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Reader

Study Record Dates

First Submitted

November 10, 2008

First Posted

November 11, 2008

Study Start

February 1, 2009

Primary Completion

August 1, 2010

Study Completion

February 1, 2011

Last Updated

July 17, 2014

Record last verified: 2014-07

Locations