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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00659932
Other study ID # 02/03/13/3.18
Secondary ID
Status Completed
Phase N/A
First received April 14, 2008
Last updated April 14, 2008
Start date May 2002
Est. completion date March 2005

Study information

Verified date December 2007
Source Hunter and New England Health
Contact n/a
Is FDA regulated No
Health authority Australia: Human Research Ethics Committee
Study type Interventional

Clinical Trial Summary

This study was designed to assess whether a cognitive behavior therapy (CBT) program for diabetes clinic patients was acceptable, improved quality of life and produced measurable change in levels of depression, anxiety and stress.


Description:

Having co-morbid anxiety or depression makes it difficult to carry out the activities for diabetes selfcare. Psychological interventions have been shown to result in improvements in HbA1C and depression. Reports on psychosocial outcomes are conflicting and there are no studies of quality of life. Our diabetes outpatient population has a higher prevalence of anxiety and depression compared to the general public and this led to the development of a group CBT intervention designed to reduce anxiety as a co-morbidity of diabetes.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date March 2005
Est. primary completion date March 2005
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Consenting attendees of the Hunter Area Diabetes Services RNH Diabetes Outpatient Clinic

Exclusion Criteria:

- Accessibility problems including:

- limited English

- developmental disability

- physical immobility

- geographical distance

- extreme age/frailty

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Immediate Cognitive behavioural therapy (CBT)
The Dealing with Anxiety CBT Group Program comprises 7 group sessions: an initial five hour session followed by 6 three hour sessions over a three month period
Delayed CBT
Commencement of the CBT Group Program is delayed 3 months

Locations

Country Name City State
Australia Royal Newcastle Hospital Newcastle New South Wales

Sponsors (1)

Lead Sponsor Collaborator
Hunter and New England Health

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hemoglobin A1C (HbA1C) 6 months No
Secondary Depression Anxiety Stress Scale (DASS) 6 months No
Secondary Diabetes Quality of Life (ADDQoL) 6 months No
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