Web-based Interactive Health Communication Application (IHCA) for Successful Home Dialysis (WISHED)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2012 by St. Joseph's Healthcare Hamilton.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
McMaster University
Information provided by (Responsible Party):
Scott Brimble, St. Joseph's Healthcare Hamilton
ClinicalTrials.gov Identifier:
NCT01403454
First received: July 21, 2011
Last updated: June 5, 2012
Last verified: June 2012
  Purpose

This study involves Chronic Kidney Disease patients that must choose the type of dialysis therapy they ultimately wish to perform. These patients receive education regarding dialysis types from nurses and Nephrologists at a Kidney Function Program. The investigators have developed a web-based Interactive Health Communication Application that could provide more education and support to patients about their dialysis choices. The investigators will compare patients that will receive usual care dialysis education versus patients that will receive additional education through this web-based application. The investigators feel that this tool may increase the proportion of patients who start home dialysis, which offers advantages such as improvement in quality of life and deceased overall healthcare costs, over hospital hemodialysis.


Condition Intervention
Chronic Kidney Disease
Behavioral: Interactive Health Communication Application
Behavioral: No Intervention: Usual Care

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Official Title: Web-based IHCA for Successful Home Dialysis

Resource links provided by NLM:


Further study details as provided by St. Joseph's Healthcare Hamilton:

Primary Outcome Measures:
  • Number of patients that start home-based dialysis. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
    Difference between groups in proportion of patients starting home-based dialysis.


Secondary Outcome Measures:
  • Number intended to start home-based dialysis [ Time Frame: 1 year ] [ Designated as safety issue: No ]
    Difference between groups in proportion of patients intending to perform home-based dialysis

  • Increase in dialysis knowledge [ Time Frame: 1 year ] [ Designated as safety issue: No ]
    Difference between groups in dialysis knowledge.

  • Increase in decision making and social support. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
    Difference between groups in decision conflict and sense of social support.

  • Mortality differences [ Time Frame: 1 year ] [ Designated as safety issue: No ]
    Difference between groups in all-cause mortality.


Estimated Enrollment: 152
Study Start Date: March 2012
Estimated Study Completion Date: January 2014
Estimated Primary Completion Date: March 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
No Intervention: usual care Behavioral: No Intervention: Usual Care
Usual care person to person dialysis modality intervention.
Active Comparator: Health Communication Application Behavioral: Interactive Health Communication Application
web-based application

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • enrolled in Kidney Function Program (KFP)
  • previously received KFP-administered dialysis modality education
  • personal access to a home computer (ie. either their own or a close friend/family member) with internet access
  • most recent eGFR < or = 20mL/min/1.73m2

Exclusion Criteria:

  • inability to provide informed consent
  • inability to use a home computer or internet
  • inability to understand English (written or spoke)
  • severe visual or auditory impairment
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01403454

Contacts
Contact: Scott K Brimble, MD 905-522-1155 ext 33787 brimbles@mcmaster.ca
Contact: Cathy Z Moreau, BSc 905-522-1155 ext 32284 cmoreau@stjoes.ca

Locations
Canada, Ontario
St. Joseph's Healthcare Hamilton Recruiting
Hamilton, Ontario, Canada, L9N 4A6
Contact: Scott K Brimble, Dr.    905-522-1155 ext 33787    brimbles@mcmaster.ca   
Principal Investigator: Scott K Brimble, Dr.         
Sponsors and Collaborators
St. Joseph's Healthcare Hamilton
McMaster University
Investigators
Principal Investigator: Scott K Brimble, MD St. Joseph's Healthcare Hamilton
  More Information

No publications provided

Responsible Party: Scott Brimble, Principal Investigator, St. Joseph's Healthcare Hamilton
ClinicalTrials.gov Identifier: NCT01403454     History of Changes
Other Study ID Numbers: 11-3536, Grant
Study First Received: July 21, 2011
Last Updated: June 5, 2012
Health Authority: Canada: Ethics Review Committee

Keywords provided by St. Joseph's Healthcare Hamilton:
chronic kidney disease
web-based application
dialysis education

Additional relevant MeSH terms:
Kidney Diseases
Renal Insufficiency, Chronic
Urologic Diseases
Renal Insufficiency

ClinicalTrials.gov processed this record on July 31, 2014