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NCT00938093 Clinical Trial

Treatment of Late-life Anxiety in Primary Care Settings

Generalized Anxiety Disorder Clinical Trial

Official title:
Treatment of Late-life Anxiety in Primary Care Settings

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00938093
Other study ID # MH65281
Secondary ID MH65281
Status Completed
Phase N/A
First received
Last updated
Start date March 2006
Est. completion date February 2009

Study information
Verified date August 2018
Source Wake Forest University Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The research study proposed is designed to examine the outcomes of a cognitive behavioral guided self-care intervention with older adults diagnosed with generalized anxiety disorder and recruited from a primary care setting. It is hypothesized that the cognitive behavioral guided self-care intervention will produce greater declines in worry and anxiety than enhanced usual care.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date February 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- age = 60 years

- a DSM-IV diagnosis of GAD

- able to read English.

Exclusion Criteria:

- current psychotherapy

- a DSM-IV diagnosis of alcohol or substance abuse

- a diagnosis of dementia or global cognitive impairment operationalized as a score of < 24 of the Mini-Mental Status Examination

- psychotic symptoms

- active suicidal ideation

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Cognitive behavioral therapy
Participants receive 10 telephone therapy sessions and an accompanying workbook focused on cognitive-behavioral techniques for managing anxiety.
• Enhanced usual care
Participants receive written information about anxiety, referrals for treatment, and an optional letter to their primary care physician.

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Wake Forest University Health Sciences National Institute of Mental Health (NIMH)

Outcome
Type Measure Description Time frame Safety issue
Primary PSWQ-A 4 months
Primary HAM-A 4 months
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