Validity and Reliability of Vietnamese Version of 17items-Hamilton Depression Rating Scale

Sponsor
University of Medicine and Pharmacy at Ho Chi Minh City (Other)
Overall Status
Unknown status
CT.gov ID
NCT04205747
Collaborator
(none)
200
15

Study Details

Study Description

Brief Summary

this reseach examines the reliability and validity of 17 items- Hamilton Depression rating scale in Vietnamese population, which has been commonly used in clinical depression practice and study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    • Cross-sectional study

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Case-Crossover
    Time Perspective:
    Cross-Sectional
    Official Title:
    Department of Psychiatry University of Medicine and Pharmacy at Ho Chi Minh City
    Anticipated Study Start Date :
    Jan 1, 2020
    Anticipated Primary Completion Date :
    Aug 1, 2020
    Anticipated Study Completion Date :
    Apr 1, 2021

    Outcome Measures

    Primary Outcome Measures

    1. validity and reliability of Vietnamese version of HDRS -17 [2020-2021]

      the study measures validity and reliability of Vietnamese version of HDRS -17

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • patients accept paticipating in reasearch
    Exclusion Criteria:
    • patients don't answer full HRDS

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Medicine and Pharmacy at Ho Chi Minh City

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nguyen Dao Uyen Trang, Resident doctor of Psychiatry, University of Medicine and Pharmacy at Ho Chi Minh City
    ClinicalTrials.gov Identifier:
    NCT04205747
    Other Study ID Numbers:
    • 3697/QD-ĐHYD
    First Posted:
    Dec 19, 2019
    Last Update Posted:
    Dec 19, 2019
    Last Verified:
    Dec 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 19, 2019