Clincosm LogoSign in Get a demo

Ability to Cope With Type 1 Diabetes

Sponsor
Baylor College of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT00206362
Collaborator
(none)
100
Enrollment
1
Location
69
Duration (Months)
1.4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to learn about the relationship that exists between coping skills and blood glucose control. In addition to this, we will study the effect of type 1 diabetes on coping skills in different age groups, genders, ethnicities, socioeconomic groups, and the duration of diabetes.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Coping with type 1 diabetes can be very difficult. Type 1 diabetes is a very unique chronic disease because it requires constant attention to several responsibilities such as daily glucose monitoring, multiple daily insulin doses, and strict diet and exercise. Several studies have shown that increased rates of poorer glucose control are a result of struggling to cope with type 1 diabetes. This may be due to the fact that many type 1 diabetics experience a feeling of exhaustion, or "burnout," after a certain period of time due to an overwhelming amount of responsibility.

    In our study we would like to determine how children's ability to cope with diabetes affects glucose control. By completing several questionnaires, we can analyze different kinds of coping skills through a complex scoring system. These scores will then be analyzed in comparison to your glucose control using HbA1c.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of Ongoing Management of Type 1 Diabetes
    Study Start Date :
    Jul 1, 2004
    Actual Primary Completion Date :
    Feb 1, 2010
    Actual Study Completion Date :
    Apr 1, 2010

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      8 Years to 21 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:

      • Subjects must be type 1 diabetic

      • English/spanish speaking

      • The legal guardian must be present.

      Exclusion Criteria:

      • Non-cognitive or mentally ill

      • Under the age of 8.0 years

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Texas Children's Hospital Houston Texas United States 77030

      Sponsors and Collaborators

      • Baylor College of Medicine

      Investigators

      • Principal Investigator: Rubina A Heptulla, MD, Baylor College of Medicine

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Rubina Heptulla, MD, Principal Investigator, Baylor College of Medicine
      ClinicalTrials.gov Identifier:
      NCT00206362
      Other Study ID Numbers:
      • 16040
      First Posted:
      Sep 21, 2005
      Last Update Posted:
      Jul 20, 2016
      Last Verified:
      Jul 1, 2016
      Individual Participant Data (IPD) Sharing Statement:
      No
      Plan to Share IPD:
      No
      Keywords provided by Rubina Heptulla, MD, Principal Investigator, Baylor College of Medicine
      Depression
      Socioeconomic status
      Type 1 diabetes mellitus
      Children
      Adolescents
      Additional relevant MeSH terms:
      Diabetes Mellitus, Type 1
      Depression

      Study Results

      No Results Posted as of Jul 20, 2016