Heart Failure Clinical Trial
— iCDMOfficial title:
Utilization of an Interactive Internet-based Platform for Managing Chronic Diseases at a Distance
NCT number | NCT01342263 |
Other study ID # | 711174 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 2011 |
Est. completion date | September 2018 |
Verified date | September 2018 |
Source | Simon Fraser University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In 2005, more then one-third of Canadians were burdened with one or more chronic diseases.
Patients with one chronic disease often have, or are at risk for, another chronic disease.
This group of complex patients represents a substantial challenge to healthcare resources.
For patients in rural communities, the opportunity to attend ambulatory care clinics is not
always an option. Additionally, the opportunity for rural patients to receive quality care
close to, or within their homes, is of great benefit as it reduces the need for extensive
travel and the potential burden of clinical visits. The use of telehealth has been identified
as an effective modality for chronic disease management and is actively promoted by national
organizations as having great promise for health service delivery in rural areas. The
Internet as a mode for healthcare delivery has numerous advantages: 1. it is ubiquitous with
increasing access in all age groups, 2. it is inexpensive, 3. it facilitates both patient
data transfer and patient feedback, thereby supporting patient self-management, 4. it is
scalable to large patient volumes, 5. it delivers health care directly to the patient and 6.
it requires minimal set-up for patients with current Internet access.
The investigators propose to develop and evaluate a multi-chronic disease management program
delivered through the Internet (with telephone supports) focused on high-impact chronic
diseases targeted to patients in rural communities.
This study will consist of a single-blinded randomized controlled trial to investigate the
efficacy of the iCDM in 318 patients with two or more of the target chronic diseases living
in rural areas. Within this Aim, the investigators will be able to address the following
research questions:
Q1. What is the effect of iCDM on healthcare utilization and patient self-management
outcomes? Q2. What is the long-term compliance to the iCDM? Q3. What is the level of patient
and provider satisfaction?
Status | Completed |
Enrollment | 234 |
Est. completion date | September 2018 |
Est. primary completion date | September 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: - two or more of the following chronic diseases; heart disease, heart failure, chronic kidney disease, diabetes and COPD - daily Internet access - able to read, write and understand English Exclusion Criteria: - patients with significant co-morbidities that may interfere with effective management - patients who have scheduled surgical procedures - patients who are unable to provide informed consent |
Country | Name | City | State |
---|---|---|---|
Canada | St. Paul's Hospital | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
Simon Fraser University | Canadian Institutes of Health Research (CIHR), Michael Smith Foundation for Health Research |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Healthcare utilization | Hospital admissions, length of hospital stay, emergency room visits, physician visits, diagnostic and lab procedures. | 24 months | |
Secondary | health-related Quality of life | Assessed by the Medical Outcomes Study 36-item Short Form survey. | 24 months | |
Secondary | Self-management | Assessed by the Health Education Impact Questionnaire (heiQ). | 24 months | |
Secondary | Social support | Assessed using the Medical Outcomes Study Social Support Scale. | 24 months | |
Secondary | Patient and Provider Experience and Satisfaction | Patients enrolled in the iCDM intervention and their family physicians will undergo a semi-structured, open-ended interview at the end of the intervention to explore patient experiences and to increase our understanding of patient factors that influence acceptance and use. | 24 months | |
Secondary | Adherence to the iCDM | Assessed through website use (logins) and completion of data entry. | 24 months | |
Secondary | Health outcomes | Assessed by the EuroQol EQ-5D-5L health questionnaire. | 24 months |
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