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Cognitive Behavioral Therapy Delivered Over the Internet for Women With Postpartum Depression

Oregon Research Institute logo

Oregon Research Institute

Status and phase

Completed
Phase 1

Conditions

Postpartum Depression

Treatments

Behavioral: Web-based CBT for PPD

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00942721
1R01MH084931-01A1 (U.S. NIH Grant/Contract)
R01MH084931 (U.S. NIH Grant/Contract)
DSIR 83-ATP

Details and patient eligibility

About

This study will develop and test a Web-based program to treat women with postpartum depression.

Full description

After a woman gives birth, she will often feel anxious, depressed, or upset. For most women, these feelings go away within a week of giving birth, but for some, postpartum depression (PPD) can develop. PPD involves long-term, more severe feelings of anxiety, depression, and despair that impair normal functioning. Untreated PPD threatens both the mental health of mothers and the development of their infants, but many cases go untreated. This may be because of the stigma of mental health treatment, limited availability of programs, cost of treatment, or difficulty finding the time to schedule trips out of the home. Treatment through a Web-based program addresses all these concerns by providing a private, cost-efficient program available anywhere with computer access. This study will develop and test a Web-based version of cognitive behavioral therapy (CBT) to treat women with PPD to determine its feasibility and acceptability.

Participation in this study will last 3 months. All participants will be offered a Web-based version of CBT for PPD. The CBT program will include guided behavioral strategies for dealing with depression, online videos of women who have used these strategies, Web forums in which participants can ask questions of peers and experts, and periodic phone coaching. The program will last 6 weeks. All participants will complete assessments at baseline, post-treatment, and 3-month follow-up. Safety monitoring questionnaires will also be completed at Weeks 2 and 4 of treatment. Assessments will include clinical interviews and questionnaires related to the following: health; depression; demographics; maternal skills, stress, and self-efficacy; Internet use, experience, and self-efficacy; behavioral self-efficacy; and program acceptability.

Enrollment

53 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Within 6 months postpartum
  • Home access to the Internet
  • Use of personal e-mail
  • Score from 12 to 20, inclusive, on the Edinburgh Postnatal Depression Scale
  • Diagnosed as having postpartum depression

Exclusion criteria

  • Current diagnosis of substance abuse, bipolar disorder, or psychotic depression
  • Currently receiving treatment for depressive symptoms, including antidepressant medication or psychotherapy
  • Currently has suicidal intentionality, lethality, access to means, and history of suicide attempts

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

53 participants in 1 patient group

Web-based CBT for PPD
Experimental group
Description:
Participants will receive Web-based CBT for PPD.
Treatment:
Behavioral: Web-based CBT for PPD

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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