Disaster Preparedness Among Families Caring for Children With Diabetes

NCT ID: NCT00781313

Last Updated: 2016-07-20

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 142 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2008-06-30
• Study Completion Date: 2009-10-31

Brief 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.

Detailed 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.

Conditions

Diabetes

Study Design

• Observational Model Type: CASE_CROSSOVER
• Study Time Perspective: CROSS_SECTIONAL

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Baylor College of Medicine

OTHER

Sponsor Role: lead

Responsible Party

Rubina Heptulla, MD

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

RUBINA A HEPTULLA, MD

Role: PRINCIPAL_INVESTIGATOR

Baylor College of Medicine

Locations

Texas Children Hospital

Houston, Texas, United States

Countries

United States

Other Identifiers

H-23261

Identifier Type: -

Identifier Source: org_study_id