Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00789100

Evaluation of Remote Patient Monitoring.

Evaluation of a Home-based Telemonitor Service

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
Brunel University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

The study is designed to evaluate the impact of home-based monitoring to support community based nursing services and care matrons in the management of patients with CHF and COPD and co-morbidities. The main issue is to design a study that will determine the impact of the use of the technology independent of other factors. A randomised controlled trial has been chosen in which equal numbers of participants with and without home-based monitoring will be followed over the study to determine differences in utilisation of healthcare services including number of hospitalisations, length of stay in hospital, GP visits and community matron and specialist community nurse home visits. The ethical issue is how to determine those that will receive home-based monitoring and those that will be denied. The study requires that participants are matched for severity of their condition in each arm and this could deny some from the potential benefits of monitoring. However, as only a limited number of home-based monitors are available and all participants will continue to receive normal health care services, we believe that those denied monitoring will not receive care that is different to patients not in the study and the ethical issues are acceptable.

Conditions

Timeline

Start date
2009-02-01
Primary completion
2010-08-01
Completion
2011-02-01
First posted
2008-11-11
Last updated
2014-07-17

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00789100. Inclusion in this directory is not an endorsement.