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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00187785
Other study ID # UMC200552
Secondary ID
Status Terminated
Phase N/A
First received September 14, 2005
Last updated January 13, 2006
Start date September 2005
Est. completion date December 2006

Study information

Verified date August 2005
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Does use of a translator or use of less than perfect Spanish diminish provider-patient communication compared to a native speaker.


Description:

Spanish speaking drop-in patients will be consented then randomized to receive care by a native Spanish speaker, an English speaker using a translator, or an English speaker with intermediate Spanish skills using Spanish. After the visit, the researcher will enquire about patient satisfaction, when the next appointment is, whether medication has been changed, and what instructions their provider gave them. Each provider will do a similar questionnaire. A blinded researcher will score a concordance of plans between provider and patient to see if there is a significant difference in retained information between the groups.


Recruitment information / eligibility

Status Terminated
Enrollment 100
Est. completion date December 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Spanish speaker

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Educational/Counseling/Training


Intervention

Behavioral:
Spanish speaker level


Locations

Country Name City State
United States UMC Family Health Center Fresno California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary retention of medical information
Secondary patient satisfaction
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