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Health Related Quality of Life and Cognitive Function Among Norwegian Dialysis Patients

Sponsor
Norwegian University of Science and Technology (Other)
Overall Status
Completed
CT.gov ID
NCT00806130
Collaborator
St. Olavs Hospital (Other)
40
Enrollment
1
Location
2
Actual Duration (Months)
20
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to assess health related quality of life and its predictors among chronic dialysis patients and to assess cognitive function using 3 different tests.

(undergraduate medical student research project; not published)

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    40 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Health Related Quality of Life and Cognitive Function Among Norwegian Dialysis Patients, a Cross-sectional Study
    Actual Study Start Date :
    Sep 1, 2008
    Actual Primary Completion Date :
    Nov 1, 2008
    Actual Study Completion Date :
    Nov 1, 2008

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:

      • Chronic kidney failure

      • Active dialysis treatment

      • Aged over 18 years

      • Able to read and answer the quality of life questionaire

      Exclusion Criteria:

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Trondheim Sør-Trøndelag Norway

      Sponsors and Collaborators

      • Norwegian University of Science and Technology
      • St. Olavs Hospital

      Investigators

      • Principal Investigator: Inger Karin Lægreid, MD, Norwegian University of Science and Technology

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Norwegian University of Science and Technology
      ClinicalTrials.gov Identifier:
      NCT00806130
      Other Study ID Numbers:
      • 4.2008.334
      First Posted:
      Dec 10, 2008
      Last Update Posted:
      Nov 9, 2017
      Last Verified:
      Nov 1, 2017
      Studies a U.S. FDA-regulated Drug Product:
      No
      Studies a U.S. FDA-regulated Device Product:
      No
      Additional relevant MeSH terms:
      Renal Insufficiency
      Kidney Failure, Chronic

      Study Results

      No Results Posted as of Nov 9, 2017