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Postpartum depression interpersonal psychotherapy trial

A randomised controlled trial to evaluate the effectiveness of telephone-based interpersonal psychotherapy for the treatment of postpartum depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN88987377
Enrollment
240
Registered
2007-03-30
Start date
2007-09-01
Completion date
Unknown
Last updated
2020-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum depression Mental and Behavioural Disorders Mild mental and behavioural disorders associated with the puerperium, not elsewhere classified

Interventions

Amended as of 12/06/2009: Interpersonal psychotherapy: one-hour session of telephone-based interpersonal psychotherapy every week for 12 weeks (i.e., or a maximum of 16 sessions for up

Sponsors

University of Toronto (Canada)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Live birth 2. Infant discharged from hospital 3. Mother between two and 24 weeks postpartum 4. Clinical diagnosis of major depression using the Structured Clinical Interview for Diagnostic and Statistical Manual of mental disorders fourth edition (DSM-IV) 5. Understands spoken English

Exclusion criteria

Exclusion criteria: Amended as of 12/06/2009: The following point was amended to: 4. Chronic depression (episode length greater than 2 years) The following point was added: 5. Current or past manic depression Initial information at time of registration: 1. Current use of antidepressant medication 2. Currently receiving any form of psychotherapy administered by a trained professional 3. Active suicidal or self-harm thoughts 4. Chronic depression (episode length greater than 2.5 years)

Design outcomes

Primary

MeasureTime frame
Postpartum depression: 12 weeks post-randomisation (immediately post-treatment for mothers in the intervention group).

Secondary

MeasureTime frame
Amended as of 12/06/2009: The following point was amended to: 4. Attachment measured with the Experiences in Close Relationships-Revised (self-report measure): 12, 24, and 36 weeks post-randomisation The following point was added: 6. Relationship quality and adjustment with the Dyadic Adjustment Scale (self-report measure): 12, 24, and 36 weeks post-randomisation Initial information at time of registration: 1. Postpartum depression (clinical diagnostic interview): 24 and 36 weeks post-randomisation (i.e., 12 and 24 weeks post-treatment for mothers in the intervention group 2. Depressive symptomatology (self-report measure): 12, 24, and 36 weeks post-randomisation 3. Anxiety measured with the Spielberger State-Anxiety Inventory (self report measure): 12, 24, and 36 weeks post-randomisation 4. Social functioning measured with the Social Adjustment Scale-Self Report (self report measure): 12, 24, and 36 weeks post-randomisation 5. Health service utilisation measured with a slightly modified version of the Health Service Utilisation and Cost of Care Questionnaire (self-report measure): from randomisation to 36 weeks post-randomisation

Countries

Canada

Contacts

Public ContactMelissa Jovellanos
melissa.jovellanos@utoronto.ca+1 (0)416 946 0929

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 26, 2026