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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01515111
Other study ID # IDRC-006
Secondary ID RITC of IDRC
Status Completed
Phase N/A
First received January 13, 2012
Last updated January 18, 2012
Start date April 2011
Est. completion date January 2012

Study information

Verified date January 2012
Source Unidad de Cirugía Cardiovascular
Contact n/a
Is FDA regulated No
Health authority Guatemala: Ministerio de Salud Pública y Asistencia Social
Study type Observational

Clinical Trial Summary

A national cross-sectional survey was conducted to evaluate recommendations on clinical preventive services and additional information on non-communicable disease prevention. Trained surveyors interviewed interns, residents and attendings of the Internal Medicine departments of all teaching hospitals in Guatemala. Analysis compared recommendation practices within and between hospitals.


Description:

A voluntary, anonymous, self-completed, cross-sectional survey was administered to all available internal medicine staff in Guatemalan teaching hospitals.

The questionnaire included: physician's demographics, work time dedicated to outpatients, knowledge of leading causes of death in Guatemala, guidelines used for non-communicable disease prevention, simulated cases asking for recommendation(s) on different preventive services for asymptomatic adults (i.e. whether they recommended them or not, appropriate frequency and starting age, preferred screening method, and availability of the service(s) at their hospital). The survey also assessed barriers faced in providing adequate services, and opinions on who should implement changes in national health care and in medical education.

The answers given by the internal medicine staff were compared with the United States Preventive Services Task Forces (USPSTF) Recommendations and Guatemalan Ministry of Health Guidelines.

Analysis compared recommendation practices within and between hospitals.


Recruitment information / eligibility

Status Completed
Enrollment 394
Est. completion date January 2012
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All interns, internal medicine residents and attendings (including department director, unit directors and regular attendings) that are currently training or working in an Internal Medicine department in any of the ten teaching hospitals in Guatemala.

Exclusion Criteria:

- Staff that is on vacations, on sick leave or suspended by any reason.

Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Guatemala Hospital Nacional Pedro Bethancourt Antigua Guatemala Sacatepequez
Guatemala Hospital Nacional de Escuintla Escuintla
Guatemala Hospital Centro Médico Militar Guatemala
Guatemala Hospital General de Enfermedad Común - IGSS Guatemala
Guatemala Hospital General San Juan de Dios Guatemala
Guatemala Hospital Hermano Pedro Guatemala
Guatemala Hospital Roosevelt Guatemala
Guatemala Hospital Universitario Esperanza Guatemala
Guatemala Unidad de Cirugía Cardiovascular Guatemala
Guatemala Hospital Regional de Occidente, San Juan de Dios Quetzaltenango

Sponsors (3)

Lead Sponsor Collaborator
Unidad de Cirugía Cardiovascular International Development Research Centre, Canada, Washington University School of Medicine

Country where clinical trial is conducted

Guatemala, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recommendations of clinical preventive services for non-communicable diseases. Recommendations on eleven clinical preventive services for non-communicable diseases were evaluated considering:
Whether they recommended them or not
Appropriate frequency and starting age
Preferred screening method
Availability of the service(s) at their hospital
After accepting to participate in the study, participants will be followed the time necesary to complete the structured questionnaire, an average of 1 hour. No
Secondary Barriers faced in providing adequate services. Self-perceived barriers to provide clinical preventive services adequately. After accepting to participate in the study, participants will be followed the time necesary to complete the structured questionnaire, an average of 1 hour. No
Secondary Opinion on who should implement changes in clinical preventive services provision. Participant's opinion on who should be responsible to implement changes in:
Chronic disease prevention in national health care
Medical education in this field.
After accepting to participate in the study, participants will be followed the time necesary to complete the structured questionnaire, an average of 1 hour. No
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