Acute Chest Triage Rapid Intervention Guided by Home Care or Telecare
ISRCTN | ISRCTN55776263 |
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DOI | https://doi.org/10.1186/ISRCTN55776263 |
Secondary identifying numbers | N/A |
- Submission date
- 22/08/2005
- Registration date
- 08/09/2005
- Last edited
- 14/12/2010
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Respiratory
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Prof Frances Mair
Scientific
Scientific
Department of General Practice and Primary Care
Division of Community-based Sciences
1 Horselethill Road
University of Glasgow
Glasgow
G12 9LX
United Kingdom
fm46c@clinmed.gla.ac.uk |
Study information
Study design | Randomised controlled trial |
---|---|
Primary study design | Interventional |
Secondary study design | Randomised controlled trial |
Study setting(s) | Not specified |
Study type | Treatment |
Scientific title | |
Study acronym | ACTRIGHT |
Study objectives | To compare a telecare intervention with traditional home care delivered by nurses to patients with acute exacerbations of COAD |
Ethics approval(s) | Not provided at time of registration |
Health condition(s) or problem(s) studied | Chronic Obstructive Airways Disease (COAD) |
Intervention | Telecare delivered in patient's own home versus traditional nurse visits. |
Intervention type | Other |
Primary outcome measure | 1. Respiratory-related Quality of Life 2. Economic outcomes |
Secondary outcome measures | 1. Nurse and patient satisfaction measures 2. Quality and reliability of equipment |
Overall study start date | 01/10/2001 |
Completion date | 30/09/2005 |
Eligibility
Participant type(s) | Patient |
---|---|
Age group | Adult |
Sex | Both |
Target number of participants | 200 across intervention (telecare) and control (home care) arms |
Key inclusion criteria | Patients referred to Accident and Emergency (A&E) for assessment, following exacerbation of COAD. Inclusion criteria include forced expiratory volume in 1 second (FEV1) <80% predicted, Systolic blood pressure (BP) >100 mmHg, pH >7.4, pO2 >6.7 kPa |
Key exclusion criteria | Exclusion criteria include pneumothorax, uncontrolled left ventricular failure (LVF), acute electrocardiogram (ECG) changes, asthma, pneumonia, and previous participation in trial. |
Date of first enrolment | 01/10/2001 |
Date of final enrolment | 30/09/2005 |
Locations
Countries of recruitment
- Scotland
- United Kingdom
Study participating centre
Department of General Practice and Primary Care
Glasgow
G12 9LX
United Kingdom
G12 9LX
United Kingdom
Sponsor information
North Liverpool Primary Care Trust (UK)
Hospital/treatment centre
Hospital/treatment centre
Cottage 2
Newhall Campus
Longmoor Lane
Liverpool
L10 1LD
England
United Kingdom
Phone | +44 (0)151 293 1900 |
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enquiries@northliverpoolpct.nhs.uk |
Funders
Funder type
Government
NHS Modernisation Fund
No information available
NHS R&D Support Funding
No information available
Results and Publications
Intention to publish date | |
---|---|
Individual participant data (IPD) Intention to share | No |
IPD sharing plan summary | Not provided at time of registration |
Publication and dissemination plan | Not provided at time of registration |
IPD sharing plan |
Study outputs
Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
---|---|---|---|---|---|
Results article | preliminary results | 01/01/2005 | Yes | No | |
Results article | results | 01/06/2008 | Yes | No |