Therapy for Depression With Co-occurring Panic or Anxiety Symptoms

NCT ID: NCT00051207

Last Updated: 2013-06-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-11-30
• Study Completion Date: 2005-08-31

Brief Summary

This 6-month study, with a 3-month follow up period, will compare the effectiveness of new and traditional psychotherapies for depression with panic or anxiety symptoms.

Detailed Description

Many depressed patients also experience significant symptoms of panic or anxiety. This study will compare the effectiveness of a new therapy called interpersonal psychotherapy for depression with panic or anxiety symptoms (IPT-PS) with that of traditional interpersonal psychotherapy for depression (IPT).

Participants are randomly assigned to receive up to 24 weeks of treatment with either IPT-PS or traditional IPT. Improvements in interpersonal functioning, quality of life, and symptoms of depression and anxiety will be assessed at the end of therapy and at a 3-month follow-up.

Conditions

Depression; Anxiety Disorders; Panic Disorder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

Interpersonal Psychotherapy (IPT)

Intervention Type: BEHAVIORAL

IPT for Depression with Co-occurring Panic and Anxiety Symptoms (IPT-PS)

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• DSM-IV diagnosis of major depression with co-existing panic or anxiety symptoms.

Exclusion Criteria

• History of manic episode(s). Patients who have had hypomanic episodes in the past will be accepted into the study, provided they meet other admission criteria and are not presenting in a current hypomanic or mixed episode.
• History of schizophrenia or schizoaffective disorder.
• Organic affective syndrome.
• Unspecified functional psychosis.
• Anorexia nervosa or bulimia nervosa. Patients meeting criteria for an eating disorder not otherwise specified will not be excluded.
• Chronic drug or alcohol abuse/dependence within the past 2 years. Patients with abuse related to episodes will not be excluded.
• DSM-IV criteria for borderline or antisocial personality disorder. Patients who meet criteria for other Axis II disorders will not be excluded.
• Inpatient treatment due to suicide risk or psychotic symptoms.
• Index episode secondary to the effect of medically prescribed drugs.
• Significant or untreated medical illness, including cardiovascular disorder, renal or liver disease, epilepsy, untreated hypertension, or unstabilized endocrine disease.
• Medical illness that would interfere with the best treatment strategy for the potential participant.
• Current treatment with an antidepressant. Patients on a stable dose of anxiolytics for at least 3 months prior to study participation who are able to maintain this dosage throughout the study will not be excluded.
• Pregnant and breast-feeding women will be accepted into the study, but will not be prescribed adjunctive medications.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Pittsburgh

OTHER

Sponsor Role: lead

Locations

Western Psychiatric Institute and Clinic - Depression and Manic Depression Program

Pittsburgh, Pennsylvania, United States

Countries

United States

Other Identifiers

DSIR AT-AS

Identifier Type: -

Identifier Source: secondary_id

R21MH061948

Identifier Type: NIH

Identifier Source: org_study_id

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