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Clinical Trials/NCT00233142
NCT00233142
Completed
Phase 2

Expressive Writing: Complementary Treatment for Diabetes

Syracuse University4 sites in 1 country187 target enrollmentSeptember 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Diabetes Mellitus
Sponsor
Syracuse University
Enrollment
187
Locations
4
Primary Endpoint
hemoglobin A1C (indicator of blood glucose)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

This study will determine whether the psychological benefits of expressive writing extend to diabetic patients, how long the benefits will last, and whether additional expressive writing "booster" sessions will lead to greater and more sustained improvement in diabetes symptoms and well-being.

Detailed Description

Diabetes is one of the leading causes of blindness, kidney failure, and nontraumatic lower extremity amputation in the United States. Conditions such as stress and depression have been shown to worsen diabetic symptoms. Data indicate that expressive writing (an activity during which individuals deal with stressful experiences by writing about them on paper) has beneficial effects on psychological and physiological outcomes. This study will determine whether diabetes patients can benefit from expressive writing. This study will also determine the duration of the benefits and the effectiveness of booster sessions in improving their diabetic symptoms. Participants will be randomly assigned to engage in expressive writing or neutral writing for 18 months. Participants in the expressive writing group will write about traumatic or stressful events; participants in the neutral writing group will write about neutral topics that do not affect them emotionally. Some participants in the expressive writing group will receive an additional 4 months of booster sessions of expressive writing. All participants will undergo interviews, blood collection, physical exams and complete clinical scales on their disease status, quality of life, and psychological well-being; these assessments will occur at study entry, every 4 months during the study, and at the end of the study.

Registry
clinicaltrials.gov
Start Date
September 2005
End Date
February 2009
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of diabetes mellitus made after age 24

Exclusion Criteria

  • Diabetes-related emergency room visit within 3 months prior to study entry
  • Use of psychiatric medication within 3 months prior to study entry
  • Visual or manual limitations that preclude reading and writing
  • Use of insulin within the first year of diabetes diagnosis
  • Pregnancy or plan to become pregnant

Outcomes

Primary Outcomes

hemoglobin A1C (indicator of blood glucose)

Time Frame: baseline, 4 months, 8 months, 12 months, and 16 months

Secondary Outcomes

  • Diabetes symptoms(baseline, 4 months, 8 months, 12 months, and 16 months)
  • quality of life(baseline, 4 months, 8 months, 12 months, and 16 months)
  • depression(baseline, 4 months, 8 months, 12 months, and 16 months)
  • cognitive function(baseline, 4 months, 8 months, 12 months, and 16 months)
  • stress levels(baseline, 4 months, 8 months, 12 months, and 16 months)

Study Sites (4)

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