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The Assessment of Quality of Life in Patients With Peritoneal Dialysis and Hemodialysis

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2011 by Taipei Medical University WanFang Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Taipei Medical University WanFang Hospital
ClinicalTrials.gov Identifier:
NCT01195519
First received: September 3, 2010
Last updated: April 22, 2011
Last verified: April 2011
History of Changes
  Purpose

Currently, lots of researches aimed at quality of life of patients with peritoneal dialysis and hemodialysis related issues. There is no study related to establish the predictive model of quality of life. This study will investigate the predictive model of quality of life in terms of peritoneal dialysis (PD) or hemodialysis (HD) patients. These results will offer the further evidence to the government to develop the effective interventions for dialysis patients. The optimal goal is to promote the quality care.


Condition
Peritoneal Dialysis
Hemodialysis

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: The Study Will Investigate the Quality of Life in PD or HD Patients

Resource links provided by NLM:

MedlinePlus related topics: Dialysis
U.S. FDA Resources

Further study details as provided by Taipei Medical University WanFang Hospital:

Estimated Enrollment: 95
Study Start Date: September 2010
Estimated Study Completion Date: September 2011
Groups/Cohorts
peritoneal dialysis and hemodialysis patients
peritoneal dialysis and hemodialysis patients

  Eligibility

Ages Eligible for Study:   20 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

peritoneal dialysis and hemodialysis patients

Criteria

Inclusion Criteria:

  • above 20 years old PD or HD patients
  • conscious clear and no psychosis
  • literate and can communicate
  • willing to participate and sign informed consent

Exclusion Criteria:

  • Not volunteer
  • subject felt weak or uncomfortable and patients decision to withdraw from the study
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01195519

Contacts
Contact: Wan Fang, hospital 02-29307930 ext 8117 huiyi072@yahoo.com.tw

Locations
Taiwan
Taipei Medical University WanFang Hospital Recruiting
Taipei, NO.111, Section 3, Hsing-Long Rd, Taipei, Taiwan
Contact: Tso-Hsiao Chen, Dean     02-29307930 ext 8117     tsohsiao@tmu.edu.tw    
Sponsors and Collaborators
Taipei Medical University WanFang Hospital
Investigators
Principal Investigator: Tso-Hsiao Chen Taipei Medical University WanFang Hospital
  More Information

Additional Information:
Click here for more information about this study  This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party: Tso-Hsiao Chen, Nephrology Dean
ClinicalTrials.gov Identifier: NCT01195519     History of Changes
Other Study ID Numbers: 99039
Study First Received: September 3, 2010
Last Updated: April 22, 2011
Health Authority: Taiwan: Department of Health

Keywords provided by Taipei Medical University WanFang Hospital:
peritoneal dialysis
hemodialysis patients

ClinicalTrials.gov processed this record on June 17, 2013