Supporting Care and Independence at Home

NCT00189852 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2016-02-19

No results posted yet for this study

Summary

The primary objective of this project is to investigate whether, in a pilot randomised controlled trial, the use of telecare (remote monitoring) technologies reduces the frequency of hospital admissions for people with chronic heart failure (CHF) and to inform the design of a larger randomised controlled trial of telecare for CHF.

Secondary objectives are:

1. To investigate whether there are benefits to users
2. To understand the impact on carers in terms of carer stress
3. To investigate whether there are benefits to the NHS and other statutory provisions
4. To investigate which users receive the greatest benefits
5. To inform whether remote monitoring of CHF patients should be provided as part of hospital discharge for a set period of time or whether it should be provided long term and be used in a preventative manner
6. To investigate whether CHF episodes can be detected and predicted based on lifestyle changes
7. To determine whether lifestyle monitoring equipment can be correlated with the information from the CHF monitoring system to determine the potential to detect deteriorating health.

Conditions

Interventions

DEVICE

Chronic heart failure monitoring system

DEVICE

Lifestyle monitoring system

Sponsors & Collaborators

  • Engineering and Physical Sciences Research Council, UK

    collaborator OTHER
  • Imperial College London

    collaborator OTHER
  • University College, London

    collaborator OTHER
  • University of Dundee

    collaborator OTHER
  • Anchor Trust

    collaborator OTHER
  • Thomas Pocklington Trust

    collaborator OTHER
  • Tunstall

    collaborator UNKNOWN
  • Barnsley Hospital

    lead OTHER

Principal Investigators

  • Mark Hawley · Barnsley Hospital NHS Foundation Trust

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-11-30
Primary Completion
2007-09-30
Completion
2009-02-28

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00189852 on ClinicalTrials.gov