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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00781313
Other study ID # H-23261
Secondary ID
Status Completed
Phase N/A
First received October 27, 2008
Last updated July 19, 2016
Start date June 2008
Est. completion date October 2009

Study information

Verified date July 2016
Source Baylor College of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The primary aim of the survey is to ascertain the emergency preparedness among our families with diabetes mellitus and to obtain a percentage of unprepared to the ones who are prepared. The secondary aim is to demonstrate the relationship between disaster preparedness and factors like socio-economic status, parent's marital status, ethnicity and those who had prior experience of a disaster to those who have not experienced a disaster.


Description:

This is a cross-sectional study. The subjects are the parent/parents/legal guardian, who will be coming to the clinic for their routine appointment for diabetes management. During the time in which the subject is waiting for the doctor or after their check-up, a research team member will approach the family and ask for their permission to administer the survey. The survey consists of a series of questions designed to ascertain the awareness towards emergency preparedness among families. After they have completed the questionnaire they would be given and/or mailed handouts to enhance their awareness towards disaster preparedness.

Potential Benefits:

This study will help to increase awareness regarding disaster preparedness among the surveyed families. Subjects and families will gain valuable information about caring for diabetes in the event of a disaster.

The potential benefit to the society is that through this study we can ascertain the primary caregiver's awareness of disaster preparedness in regard to a family member with a chronic illness. We will suggest measures to improve their competency towards dealing with disasters. We will be providing educational literature to the primary care givers in the form of handouts at the end of the survey.


Recruitment information / eligibility

Status Completed
Enrollment 142
Est. completion date October 2009
Est. primary completion date January 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Subjects include families of children with type 1 and type 2 diabetes mellitus attending the Diabetes/ Endocrine Clinic at Texas Children Hospital.

Exclusion Criteria:

- Subjects excluded are families of Children with illnesses other than type 1 and type 2 diabetes mellitus attending the Diabetes/ Endocrine Clinic at Texas Children Hospital.

Study Design

Observational Model: Case-Crossover, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
United States Texas Children Hospital Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Baylor College of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary aim is to ascertain the emergency preparedness among our families with diabetes mellitus and to obtain a percentage of unprepared to the ones who are prepared. September 2008 No
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