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Validation of the geriatric anxiety inventory in a duloxetine clinical trial for elderly adults with generalized anxiety disorder

Published online by Cambridge University Press:  30 April 2015

Susan G. Ball ,
Sarah Lipsius  and
Rodrigo Escobar
Susan G. Ball*
Affiliation:
Eli Lilly and Company, Corporate Center DC 1542, Indianapolis, IN 46285, USA Indiana University School of Medicine, Indianapolis, IN 46202, USA
Sarah Lipsius
Affiliation:
Biostatistician InVentiv Health Clinical, 1787 Sentry Parkway, Suite 300, Bldg 16, Blue Bell, PA 19422, USA
Rodrigo Escobar
Affiliation:
Eli Lilly and Company DC 1546, Corporate Center, Indianapolis, IN 46285, USA
*
Correspondence should be addressed to: Susan G. Ball, Ph.D. Principal Clinical Research Scientist, Eli Lilly and Company, Corporate Center DC 1542, Indianapolis, IN 46285, USA. Phone: (317) 292-8735; Fax: (317) 277-2049. Email: ballsg@lilly.com.
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Abstract

Background:

The Generalized Anxiety Inventory (GAI) has been developed for use in the assessment of anxiety symptoms in older adults (≥ 65 years), but previous validation work has not examined the psychometric qualities of the instrument in relation to treatment. The objective of this study was to examine the performance of the GAI for its internal reliability, convergent and divergent validity, and its sensitivity to treatment.

Methods:

Elderly patients with generalized anxiety disorder (GAD) participated in a 10-week double-blind study of duloxetine treatment for patients with GAD. Anxiety symptoms were assessed with the Hamilton Anxiety Rating Scale (HAMA), the Hospital Anxiety and Depression Scale (HADS) anxiety and depression subscales, and the GAI. Internal reliability of the GAI was assessed with Cronbach's α. Correlations among the HAMA, HADS, and GAI scores were analyzed to determine convergent and divergent validity. Patients were also compared on remission status using recommended cut-off scores for the GAI.

Results:

Patients with GAD, who were at least 65 years of age, were randomly assigned to double-blind treatment with either duloxetine (N = 151) or placebo (N = 140) for 10 weeks acute therapy. The mean change on the GAI was significantly greater with duloxetine compared with placebo treatment (−8.36 vs. −4.96, respectively, p ≤ 0.001). The GAI demonstrated good internal consistency, good convergent and divergent validity, but suggested cut-off values for caseness with the GAI did not correspond to remission status as measured by the HAMA.

Conclusions:

Within an elderly patient population with GAD, the GAI demonstrated sound psychometric qualities and sensitivity to change with treatment.

Keywords

anxietyclinical assessmentscales
Type
Research Article
Information
International Psychogeriatrics , Volume 27 , Issue 9 , September 2015 , pp. 1533 - 1539
Copyright
Copyright © International Psychogeriatric Association 2015 

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