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

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ClinicalTrials.gov Identifier: NCT01195519
Recruitment Status : Unknown
Verified April 2011 by Taipei Medical University WanFang Hospital.
Recruitment status was:  Recruiting
First Posted : September 6, 2010
Last Update Posted : April 26, 2011
Sponsor:
Information provided by:

Study Description
Brief Summary:
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 or disease
Peritoneal Dialysis Hemodialysis

Study Design

Study Type : Observational
Estimated Enrollment : 95 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: The Study Will Investigate the Quality of Life in PD or HD Patients
Study Start Date : September 2010
Estimated Study Completion Date : September 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dialysis
U.S. FDA Resources

Groups and Cohorts

Group/Cohort
peritoneal dialysis and hemodialysis patients
peritoneal dialysis and hemodialysis patients


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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:
Responsible Party: Tso-Hsiao Chen, Nephrology Dean
ClinicalTrials.gov Identifier: NCT01195519     History of Changes
Other Study ID Numbers: 99039
First Posted: September 6, 2010    Key Record Dates
Last Update Posted: April 26, 2011
Last Verified: April 2011

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