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 |
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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
- 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: