NCT01195519

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
95

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Sep 2010

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2010

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

September 3, 2010

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 6, 2010

Completed
12 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2011

Completed
Last Updated

April 26, 2011

Status Verified

April 1, 2011

First QC Date

September 3, 2010

Last Update Submit

April 22, 2011

Conditions

Peritoneal DialysisHemodialysis

Keywords

peritoneal dialysishemodialysis patients

Study Arms (1)

peritoneal dialysis and hemodialysis patients

peritoneal dialysis and hemodialysis patients

Eligibility Criteria

Age20 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

peritoneal dialysis and hemodialysis patients

You may qualify if:

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

You may not qualify if:

  • Not volunteer
  • subject felt weak or uncomfortable and patients decision to withdraw from the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taipei Medical University WanFang Hospital

Taipei, No.111, Section 3, Hsing-Long Rd, Taipei, Taiwan

RECRUITING

Related Links

Study Officials

  • Tso-Hsiao Chen

    Taipei Medical University WanFang Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Wan Fang, hospital

CONTACT

02-29307930huiyi072@yahoo.com.tw

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 3, 2010

First Posted

September 6, 2010

Study Start

September 1, 2010

Study Completion

September 1, 2011

Last Updated

April 26, 2011

Record last verified: 2011-04

Locations

TW(1)