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Pharmacological Treatment of Generalized Anxiety Disorder in the Elderly (Sert-GAD)

Primary Purpose

Generalized Anxiety Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
sertraline 50 mg daily
sertraline 100 mg daily
Placebo 50 or 100 mg
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Generalized Anxiety Disorder focused on measuring sertraline, pharmacotherapy, geriatric

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males and females of any race, ages 60 years and older.
  • Willingness to accept randomization.
  • Subjects who meet current (Diagnostic and Statistical Manual of Psychiatric Disorders forth edition (DSM-IV) criteria for a principal diagnosis of GAD
  • Patients must have a minimum of a "moderately ill" rating on the Clinicians Global Impression-Severity Scale for GAD.
  • Patients will have a score of 10 or more on the Hospital Anxiety and Depression Rating Scale (HADS) Anxiety subscale.
  • Subjects entering the study will be free of psychotropic medications.

Exclusion Criteria:

  • Subjects with DSM-IV current major depressive episode will be excluded.
  • Subjects who exhibit suicidal ideation or are judged to be a significant suicide risk.
  • Subjects who meet DSM-IV criteria for a substance (drug and alcohol) abuse and dependence disorder within the past 6 months
  • Subjects who meet current or past DSM-IV criteria for psychotic disorder, or bipolar disorder.
  • Subjects who meet DSM-IV criteria for dementia.
  • Subjects with DSM-IV current major depressive episode will be excluded.
  • Subjects who exhibit suicidal ideation or are judged to be a significant suicide risk.
  • Subjects who meet DSM-IV criteria for a substance (drug and alcohol) abuse and dependence disorder within the past 6 months
  • Subjects who meet current or past DSM-IV criteria for psychotic disorder, or bipolar disorder.
  • Subjects who meet DSM-IV criteria for dementia.

Sites / Locations

  • VA Medical Center, Tuscaloosa
  • Miami VA Healthcare System, Miami, FL
  • Ralph H Johnson VA Medical Center, Charleston

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Sertraline 50mg

Sertraline 100mg

Placebo

Arm Description

sertraline 50 mg daily

sertraline 100mg daily

placebo 50 or 100mg

Outcomes

Primary Outcome Measures

Comparisons of End of Study HAM-A Score Means for Sertraline 50 mg vs Placebo, Sertraline 100 mg vs Placebo, and Sertraline 50 mg vs. Sertraline 100 mg
Least squares (LS) means estimate and p-value from mixed effects model with baseline and site as covariates and Tukey-Kramer adjustment for multiple comparisons Hamilton Rating Scale for Anxiety (HAM-A) is a widely used rating scale for anxiety describes the presence/absence of the severity of anxiety symptoms. It's clinician-rated scale of 14 items rated from 0-4. Generally, total score of <17 is mild anxiety; 18-24 is mild to moderate, and 25 and up is moderate to severe.

Secondary Outcome Measures

Full Information

First Posted
June 17, 2008
Last Updated
November 2, 2016
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT00701675
Brief Title
Pharmacological Treatment of Generalized Anxiety Disorder in the Elderly
Acronym
Sert-GAD
Official Title
Pharmacological Treatment of Generalized Anxiety Disorder in the Elderly
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
September 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Generalized anxiety disorder (GAD) is a very common disorder in the geriatric population with prevalence rates reaching 7% and even higher rates of 8% among elderly veterans. However, despite such high prevalence treating clinicians are presently forced to address treatment issues in this population without the guidance of scientific data. This proposal aims to begin to address this void. In light of emerging information regarding efficacy of the newer anti anxiety agents, specifically the selective serotonin reuptake inhibitors (SSRIs), in the treatment of young adult GAD patients it is time to prospectively evaluate the safety and efficacy of these medications in the treatment of elderly GAD patients. Therefore, this study will examine the effects and safety of the SSRI sertraline at different doses (50mg and 100mg per day) for older patients with GAD.
Detailed Description
Generalized anxiety disorder (GAD) is a serious and distinct illness that occurs in significant numbers, affecting at least 7 million people in the United States alone. The prevalence of GAD is higher in the primary care setting with rates twice as high as the rates reported in community samples. GAD is a life-long disorder with low remission rates, resulting in high disability and morbidity. Of significance are emerging epidemiological data suggesting that GAD is highly prevalent in the geriatric population with prevalence rates ranging from 1.9% to 7.1% and accounting for the majority of anxiety disorder cases in this age group. More alarming is the fact that the presence of anxiety symptoms leads to considerable functional impairment, increased morbidity, and mortality among the affected elderly population, thus leading to increases in the costs of their care. However, despite advances made in GAD treatment in the adult population, no prospective data are presently available on the treatment of GAD in the elderly population, forcing clinicians to provide treatment without the guidance of scientific data. These findings are of particular relevance to the Veterans Affairs Health Care System where the average age of patients treated in primary care clinics is currently 60-64 years. The present application focuses on this target subpopulation of elderly veterans. This proposal aims to provide evidence-based guidelines for pharmacological management of elderly veterans suffering from generalized anxiety disorder. This will be accomplished by conducting a clinical trial in elderly veterans suffering from GAD by evaluating the efficacy and safety of sertraline - a proven anxiolytic compound widely used in the young adult population. We believe that this proposed study will be one of the first studies in this area. Thus, it may also serve as a first step in a future line of research aimed at developing comprehensive pharmacological and psychosocial interventions in the treatment of anxiety in the elderly. (b) HYPOTHESIS/RESEARCH QUESTIONS Study Hypothesis In a double-blind, placebo-controlled trial in elderly veterans diagnosed with GAD, sertraline will be more effective and equally safe as placebo in reducing symptoms of generalized anxiety disorder. Research Question Will the presence of differences in pharmacokinetics (PK) (i.e., mean population values of steady state plasma concentrations) and plasma levels of sertraline explain differences in efficacy and side effect profile between and within the two fixed sertraline doses studied, if detected? (c) SPECIFIC OBJECTIVE The objective of the proposed study is to conduct a multi-site, double-blind, placebo-controlled trial evaluating the efficacy and safety of sertraline at fixed doses vs. placebo in the treatment of GAD among elderly primary care outpatient veterans.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Generalized Anxiety Disorder
Keywords
sertraline, pharmacotherapy, geriatric

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sertraline 50mg
Arm Type
Experimental
Arm Description
sertraline 50 mg daily
Arm Title
Sertraline 100mg
Arm Type
Experimental
Arm Description
sertraline 100mg daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo 50 or 100mg
Intervention Type
Drug
Intervention Name(s)
sertraline 50 mg daily
Other Intervention Name(s)
zoloft 50 mg daily
Intervention Description
50 mg daily
Intervention Type
Drug
Intervention Name(s)
sertraline 100 mg daily
Other Intervention Name(s)
zoloft 100mg daily
Intervention Description
100 mg daily
Intervention Type
Drug
Intervention Name(s)
Placebo 50 or 100 mg
Other Intervention Name(s)
50mg or 100mg matching placebo
Intervention Description
50mg or 100mg matching placebo
Primary Outcome Measure Information:
Title
Comparisons of End of Study HAM-A Score Means for Sertraline 50 mg vs Placebo, Sertraline 100 mg vs Placebo, and Sertraline 50 mg vs. Sertraline 100 mg
Description
Least squares (LS) means estimate and p-value from mixed effects model with baseline and site as covariates and Tukey-Kramer adjustment for multiple comparisons Hamilton Rating Scale for Anxiety (HAM-A) is a widely used rating scale for anxiety describes the presence/absence of the severity of anxiety symptoms. It's clinician-rated scale of 14 items rated from 0-4. Generally, total score of <17 is mild anxiety; 18-24 is mild to moderate, and 25 and up is moderate to severe.
Time Frame
11 weeks from baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females of any race, ages 60 years and older. Willingness to accept randomization. Subjects who meet current (Diagnostic and Statistical Manual of Psychiatric Disorders forth edition (DSM-IV) criteria for a principal diagnosis of GAD Patients must have a minimum of a "moderately ill" rating on the Clinicians Global Impression-Severity Scale for GAD. Patients will have a score of 10 or more on the Hospital Anxiety and Depression Rating Scale (HADS) Anxiety subscale. Subjects entering the study will be free of psychotropic medications. Exclusion Criteria: Subjects with DSM-IV current major depressive episode will be excluded. Subjects who exhibit suicidal ideation or are judged to be a significant suicide risk. Subjects who meet DSM-IV criteria for a substance (drug and alcohol) abuse and dependence disorder within the past 6 months Subjects who meet current or past DSM-IV criteria for psychotic disorder, or bipolar disorder. Subjects who meet DSM-IV criteria for dementia. Subjects with DSM-IV current major depressive episode will be excluded. Subjects who exhibit suicidal ideation or are judged to be a significant suicide risk. Subjects who meet DSM-IV criteria for a substance (drug and alcohol) abuse and dependence disorder within the past 6 months Subjects who meet current or past DSM-IV criteria for psychotic disorder, or bipolar disorder. Subjects who meet DSM-IV criteria for dementia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olga Brawman-Mintzer, MD
Organizational Affiliation
Ralph H Johnson VA Medical Center, Charleston
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Medical Center, Tuscaloosa
City
Tuscaloosa
State/Province
Alabama
ZIP/Postal Code
35404
Country
United States
Facility Name
Miami VA Healthcare System, Miami, FL
City
Miami
State/Province
Florida
ZIP/Postal Code
33125
Country
United States
Facility Name
Ralph H Johnson VA Medical Center, Charleston
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29401-5799
Country
United States

12. IPD Sharing Statement

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Pharmacological Treatment of Generalized Anxiety Disorder in the Elderly

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