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A research study to evaluate the "current management" of patients with chronic heart failure with the "usual care" plus "additional" remote monitoring by study doctors and a research nurse

A prospective randomised controlled trial to evaluate the effects of remote physiological monitoring for chronic heart failure (CHF) on emergency department presentations and unplanned hospital admissions for chronic heart failure.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000082202
Acronym
WATCH Study
Enrollment
102
Registered
2009-02-04
Start date
2008-11-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Physiological monitoring of community patients with at-risk chronic heart failure randomised into one of 2-groups. Group 1 -Current management by the Sir Charles Gairdner Hospital Heart Failure Clinic including written Patient Education + Phone Support compared with Group 2 - Home computer recording of physiological measurements by the patient and centrally evaluated by the Trial Nurse / Doctor. We hypothesise that daily review of physiological parameters will facilitate early medical intervention and thereby reduce emergency department presentations and unplanned hospital admissions for chronic heart failure.

Interventions

12 months daily home electronic measurements by patients of their physiological parameters - 1. Pulse rate & Electrocardiograph (ECG) by placing their hands on an "external monitoring plate" 2. Temperature & Oxygen Saturation by digital pulse oximetry 3. Blood pressure by automated cuff measurements 4. Weight by external scales. The above modules are attached to the remote monitoring system and measurements are transmitted via the patients telephone line to a central monitoring database and acce

12 months daily home electronic measurements by patients of their physiological parameters - 1. Pulse rate & Electrocardiograph (ECG) by placing their hands on an "external monitoring plate" 2. Temperature & Oxygen Saturation by digital pulse oximetry 3. Blood pressure by automated cuff measurements 4. Weight by external scales. The above modules are attached to the remote monitoring system and measurements are transmitted via the patients telephone line to a central monitoring database and accessed by the study Doctor and Research Nurse to facilitate early medical intervention. 5. Daily Patient Health Diary entries will be recorded manually and entered electronically at a later time by trial staff. 6. Quality of Life Questionnaires will be recorded by trial staff addressing each question over the telephone with the patient. 7. Health Record review by trial staff on site will be manual and electronic. 8. General Practitioner visits and communication will be recorded manually by the patient in the daily Patient Health Diary. Actions/treatments initiated during patient General Practitioner visits will be clarified by trial staff with the relevant General Practitioner as necessary.

Sponsors

Curtin University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Age > 65 years, primary diagnosis of chronic heart failure, New York Heart Association (NYHA) > Grade 2, can give informed consent

Exclusion criteria

Documented cognitive deficit, non-english speaking or participation in another trial

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026