Telephone-Based Care Management Program for Individuals With Anxiety Disorders

Phase 3

Completed

• Conditions: Anxiety Disorders; Panic Disorder
• Interventions: Behavioral: Telephone-based collaborative care; Behavioral: Usual care

• Registration Number: NCT00158327
• Lead Sponsor: University of Pittsburgh

Brief Summary

This study will determine the impact of a telephone-based care management program for primary care patients with panic disorder or generalized anxiety disorder.

Detailed Description

Numerous studies have shown that telephone-based collaborative care programs may be an effective way to monitor the quality of life of individuals with mental health issues such as anxiety disorders. With regular monitoring through telephone conversations, health care providers can gain information from their patients in a convenient forum. This study will determine whether a telephone-based care management program can improve anxiety symptoms, alcohol abuse, employment patterns, use of health care services, and health-related quality of life for individuals with panic disorder or generalized anxiety disorder (GAD).

Participants will be randomly assigned to receive either usual care or a telephone-based collaborative care program for 12 months. Usual care may include one or more of several different treatments such as pharmacotherapy and cognitive behavioral therapy; the treatments will be chosen by participants' physicians. Participants assigned to the telephone-based program will have a choice of what type of treatment they will receive; the choices will include pharmacotherapy, workbook training designed to help participants improve their coping skills, referral to a community mental health specialist, or some combination of these treatments.

Participants receiving usual care will continue their treatment for 12 months. After 12 months, these participants will undergo interviews and complete self-report scales for assessment of their anxiety symptoms, health care use, alcohol use, and quality of life. Their participation in the trial will end after 12 months.

Participants in the telephone intervention group will receive telephone calls 1 to 2 times every month for 12 months. During the calls, participants will be asked about their attitude toward and adherence to their treatment regimen. They will also be asked about recent episodes of anxiety they have experienced and what coping techniques they have used. Monthly follow-up calls will continue for an additional 12 months after the first year of the study; this will help determine the long-term effectiveness of the telephone-based intervention.

Study Timeline

• Study Start: 2004-03
• Study First Submitted: 2005-09-07
• Study First Submitted QC: 2005-09-07
• Study First Posted: 2005-09-12
• Primary Completion: 2010-06
• Study Completion: 2011-02
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-21
• Last Update Posted: 2014-01-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 360

Inclusion Criteria

• Diagnosis of panic disorder or generalized anxiety disorder
• Score of 7 or higher on the Panic Disorder Severity Scale score OR a score of 14 or higher on the Structured Interview Guide for the Hamilton Anxiety Scale
• Life expectancy greater than 1 year
• Have a household telephone and can be contacted by phone for the duration of the study
• Able to read and write in English

Exclusion Criteria

• Presently receiving treatment for a psychiatric disorder from a mental health specialist
• At risk for suicide
• History of bipolar disorder
• Dependence on alcohol or other substances within 6 months prior to study entry
• Organic anxiety syndromes, including those secondary to medical illness or drugs
• Unstable medical conditions that would interfere with the study
• Plan to leave their primary care source during the study or for 1 year after study completion

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Telephone-based collaborative care	Participants will receive telephone-based collaborative care
2	Usual care	Participants will receive usual care

Primary Outcome Measures

Name	Time	Method
Health-related quality of life (SF-36 MCS)	Measured at Month 12

Secondary Outcome Measures

Name	Time	Method
Generalized anxiety symptoms	Measured at Month 12
PHQ-9	Measured at Month 12
Alcohol use	Measured at Month 12
Health services utilization	Measured at Month 12
Health care costs	Measured at Month 12
Panic disorder severity scale (PDSS)	Measured at Month 12

Trial Locations

Locations (1)

University of Pittsburgh; 🇺🇸 Pittsburgh, Pennsylvania, United States