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Interpersonal and Social Rhythm Therapy Enter the Brief Title for Protocol IRB 09-003781> (IPSRT)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01037283
First Posted: December 22, 2009
Last Update Posted: September 16, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Astrid Hoberg, Mayo Clinic
  Purpose
In patients with bipolar disorder referred for psychotherapy, is interpersonal and social rhythm therapy delivered in a group psychotherapy format over 2-3 weeks feasible? This project will help determine if interpersonal social rhythm therapy can be delivered in the programmatic format being considered for the outpatient mood program.

Condition Intervention
Bipolar Disorder, Depressed Behavioral: Interpersonal and Social Rhythm Therapy

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Feasibility of Interpersonal and Social Rhythm Therapy for Outpatients With Bipolar Disorder

Resource links provided by NLM:


Further study details as provided by Astrid Hoberg, Mayo Clinic:

Primary Outcome Measures:
  • Symptom improvement and patient satisfaction with group and programmatic format in the delivery of interpersonal and social rhythm therapy. [ Time Frame: 3 months ]

Enrollment: 9
Study Start Date: October 2009
Study Completion Date: August 2010
Primary Completion Date: May 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Interpersonal and Social Rhythm Therapy
All participants receive eight sessions of Interpersonal and Social Rhythm Therapy.
Behavioral: Interpersonal and Social Rhythm Therapy
Interpersonal and Social Rhythm Therapy delivered in two individual therapy sessions and six group therapy sessions.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Adult patients with a confirmed diagnosis of Bipolar disorder in a depressed phase.

Referral for Interpersonal and Social Rhythm Therapy

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01037283


Sponsors and Collaborators
Mayo Clinic
Investigators
Principal Investigator: Astrid Hoberg, RN, CNS Mayo Clinic
  More Information

Responsible Party: Astrid Hoberg, Clinical Nurse Specialist, Mayo Clinic
ClinicalTrials.gov Identifier: NCT01037283     History of Changes
Other Study ID Numbers: 09-003781
First Submitted: December 18, 2009
First Posted: December 22, 2009
Last Update Posted: September 16, 2011
Last Verified: September 2011

Keywords provided by Astrid Hoberg, Mayo Clinic:
Bipolar
Depressed

Additional relevant MeSH terms:
Bipolar Disorder
Depression
Bipolar and Related Disorders
Mental Disorders
Behavioral Symptoms