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Trial record 12 of 5359 for:    "Depressive Disorder" [DISEASE] AND Behavioral

Behavioral Activation for Perinatal Depression

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. Identifier: NCT01401231
Recruitment Status : Completed
First Posted : July 25, 2011
Last Update Posted : October 13, 2017
National Institute of Mental Health (NIMH)
HealthPartners Institute
Information provided by (Responsible Party):
Kaiser Permanente

Brief Summary:
This pilot study will examine the feasibility, acceptability, and effectiveness of a brief behavioral activation psychotherapy for women with perinatal depression.

Condition or disease Intervention/treatment Phase
Depression During Pregnancy Behavioral: Behavioral activation psychotherapy Other: Usual care Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 163 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Pilot Trial of Behavioral Activation Psychotherapy for Perinatal Depression
Study Start Date : August 2011
Actual Primary Completion Date : October 2014
Actual Study Completion Date : October 2014

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: Behavioral Activation
Behavioral activation psychotherapy
Behavioral: Behavioral activation psychotherapy
Up to 10 sessions of behavioral activation psychotherapy delivered in person or by telephone.

Placebo Comparator: Usual Care
Continued care as usual
Other: Usual care
Continued usual care (could include referral for medication or psychotherapy)

Primary Outcome Measures :
  1. PHQ9 Depression Score [ Time Frame: 3 months post-partm ]
    Mean PHQ9 depression score 3 months postpartum

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

- Pregnant PHQ9 Depression Score of 15 or greater Receiving prenatal care at one of the participating sites

Exclusion Criteria:

- Known diagnosis of bipolar or psychotic disorder Active substance dependence Immediate risk of self harm Immediate need for inpatient mental health treatment

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 identifier (NCT number): NCT01401231

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United States, Washington
Group Health Cooperative
Seattle, Washington, United States, 98101
Sponsors and Collaborators
Kaiser Permanente
National Institute of Mental Health (NIMH)
HealthPartners Institute

Publications automatically indexed to this study by Identifier (NCT Number):
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Responsible Party: Kaiser Permanente Identifier: NCT01401231     History of Changes
Other Study ID Numbers: U19MH092201 ( U.S. NIH Grant/Contract )
U19MH092201 ( U.S. NIH Grant/Contract )
First Posted: July 25, 2011    Key Record Dates
Last Update Posted: October 13, 2017
Last Verified: October 2017

Keywords provided by Kaiser Permanente:

Additional relevant MeSH terms:
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Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders