Psychosocial Therapy Plus Maintenance Pharmacotherapy for Treating Bipolar Disorder

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT00227968
Collaborator
(none)
181
1
85
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Study Details

Study Description

Brief Summary

This study will evaluate the effectiveness of interpersonal and social rhythm therapy (IPSRT) versus clinical status and symptom response therapy (CSSRT) in reinforcing the treatment of bipolar disorder in individuals who are currently undergoing medication treatment for the disorder.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Interpersonal Social Rhythm Therapy (IPSRT)
  • Behavioral: Clinical Status and Symptom Response Therapy (CSSRT)
Phase 4

Detailed Description

Bipolar disorder is a serious medical illness that causes shifts in a person's mood, energy, and ability to function. These changes are drastic, and can result in damaged relationships, poor job or school performance, and suicide. Bipolar disorder is also known as manic-depressive disorder because it is characterized by episodes of mania and depression. Some signs and symptoms of a manic episode include the following: increased energy, activity, and restlessness; excessively "high," overly good mood; and extreme irritability. Some signs and symptoms of a depressive episode include the following: sad, anxious, or empty mood; feelings of hopelessness or pessimism; and feelings of guilt, worthlessness, or helplessness. Bipolar disorder is most effectively treated using a strategy that combines medication and psychosocial treatment. This study will evaluate the effectiveness of IPSRT versus CSSRT in reinforcing the treatment of bipolar disorder in individuals who are currently undergoing maintenance medication treatment for the disorder.

Participants in this open-label study will be randomly assigned to one of two treatment strategies: IPSRT or CSSRT. All participants will attend study visits once a week until they have been stable for 4 weeks (acute phase). At this point, they will attend study visits every other week for 12 weeks (continuation phase), and then once a month for 18 months or until another depressive or mixed episode occurs (maintenance phase). Participants who experience a recurrence will be treated with medication and the type of therapy they were assigned upon study entry (IPSRT or CSSRT). These participants will continue to be followed for a period of time equivalent to their remainder of time in the study had they not experienced a recurrence. Outcomes will be measured at Week 12 of the continuation phase and Week 18 of the maintenance phase.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Maintenance Therapies in Bipolar Disorder
Study Start Date :
Mar 1, 1995
Study Completion Date :
Apr 1, 2002

Outcome Measures

Primary Outcome Measures

  1. Time to stabilization in the acute phase and time to recurrence in the maintenance phase []

Secondary Outcome Measures

  1. Measured at Week 12 of the continuation phase and Week 18 of the maintenance phase: Somatic Symptoms Checklist []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of bipolar disorder

  • Currently in the third episode of mania or major depression

  • History of one other episode of major depression within 5 years prior to study entry

Exclusion Criteria:
  • Currently in the first episode of mania or schizo-affective disorder (manic type)

  • Rapid cycling drug or alcohol abuse

  • Unstable medical illness

  • Pregnant

  • Index episode caused by medically prescribed drugs

Contacts and Locations

Locations

Site City State Country Postal Code
1 Western Psychiatric Institute and Clinic Pittsburgh Pennsylvania United States 15213

Sponsors and Collaborators

  • University of Pittsburgh

Investigators

  • Principal Investigator: Ellen Frank, PhD, University of Pittsburgh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00227968
Other Study ID Numbers:
  • R37MH029618-95
  • 950310
First Posted:
Sep 28, 2005
Last Update Posted:
Jun 25, 2013
Last Verified:
Jun 1, 2013
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 25, 2013