- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02310529
Interpersonal Psychotherapy for Maternal Depression
Randomized Control Trial of an Interpersonal Psychotherapy for Maternal Depression
Depression related to pregnancy frequently presents postpartum depression, which has deteriorating and lasting negative effects, not only on infant and child well being but also on mother's and father's mental health (Nancy K et al 2009). It is therefore important to introduce interventions aiming to improve mental health of mothers that could minimize the risk of diseases, and have positive effect child's on physical and psychological developmental wellbeing.
Therefore, this project has been designed to assess the effectiveness of Interpersonal Psychotherapy for Postnatal Depression in Pakistan.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Prevalence of depression in the postnatal period is 10% to 17 % in western world ( O 'Hara and Swain 1996; Josseffson et al 2001; Yoshida et al 2001) and 23% to 36% in the developing world (Rahman et al 2003; Patel et al 2002; Husain et al 2006).
In developed countries, studies indicate that maternal depression is associated with long-term emotional, cognitive and behavioral problem in children. There is evidence of link between maternal psychopathology to physical health of child. Research evidence also indicates that long-term negative impact of postnatal depression is on the mother's mental health, on infant's development and on the marital relationship (Reay, Fisher, Robertson, Adams and Owen 2005).
because of high prevalence of maternal depression in low income countries like Pakistan, the present study is designed to test the effectiveness of Interpersonal Psychotherapy for women with maternal depression. The participants will be recruited from Civil hospital Karachi and also from three different communities. total 50 participants will be recruited and randomized to 2 groups: either intervention or TAU group. Assessment will be done on baseline, after completion of intervention and 3 months after completion of intervention. Assessment will include Edinburg Postnatal depression scale, Patient Health Questionnaire-9, Generalized Anxiety Disorder-7 and Rosenberg Self Esteem scale. Participants in intervention group will receive 12 sessions of Interpersonal Psychotherapy (IPT)
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Sind
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Karachi, Sind, Pakistan
- Bhitaiabad
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Sindh
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Karachi, Sindh, Pakistan, 72000
- Civil Hospital Karachi
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Karachi, Sindh, Pakistan
- Bilal Colony
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Karachi, Sindh, Pakistan
- Yousuf Goth
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Mothers age 18 years and above older with child below 3 years of age
- Meet the criteria for mild to moderate depressive symptoms on (EPDS (cut off score above 10) and
- Were resident of trial catchment area were included in the study.
Exclusion Criteria:
- Mothers who were suffering from severe depression, with diagnosed learning or physical disability or
- Any major psychiatric illness other than maternal depression, with Alcohol and substance dependent or
- Actively suicidal were excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Interpersonal Psychotherapy
Interpersonal Psychotherapy will be delivered to Intervention group.
The intervention group will be further divided into 3 groups (8 depressed mothers in each group).
IPT is 12-16 week treatment, contains a supportive element, an educational element, parenting element and an interpersonal relationship element.
Its goals include helping mothers feel supportive, empowered and confident about their parenting abilities, which will directly influence in reducing their depressive symptoms as well as resolution of interpersonal conflicts.
Groups will assist people who have become withdrawn, isolated and disconnected.
Intervention will be delivered by trained clinical psychologists.
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Interpersonal Psychotherapy will be delivered to Intervention group. The intervention group will be further divided into 3 groups (8 depressed mothers in each group).IPT is 12-16 week treatment, contains a supportive element, an educational element, parenting element and an interpersonal relationship element. Its goals include helping mothers feel supportive, empowered and confident about their parenting abilities, which will directly influence in reducing their depressive symptoms as well as resolution of interpersonal conflicts. Groups will assist people who have become withdrawn, isolated and disconnected. Intervention will be delivered by trained clinical psychologists.
Other Names:
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No Intervention: Treatment as usual
Patients including in this group will be taking only treatment as usual (in Pakistan it means that participants attending in outpatients' clinic at regular intervals and may or may not be taking prescribed medication).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Edinberg Postnatal Depression Scale (EPDS) To test the feasibility and acceptability of interpersonal psychotherapy in women suffering from postnatal depression.
Time Frame: 3 months
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EPDS will be used to assess depression
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3 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient Health Questionnaire-9 (PHQ-9)
Time Frame: 3 and 6 Months
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PHQ-9 will be used to assess severity of depression
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3 and 6 Months
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Generalized Anxiety Disorder-7 (GAD-7)
Time Frame: 3 and 6 Months
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GAD-7 will be used to assess severity of anxiety
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3 and 6 Months
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Rosenberg Self Esteem Scale (RSES)
Time Frame: 3 and 6 Months
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This scale will ne used to assess self esteem
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3 and 6 Months
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Collaborators and Investigators
Investigators
- Study Director: Dr. Nusrat Husain, PILL
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PILL-IPT
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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