Randomised Control Trial of a Complex Intervention for Postnatal Depression
Primary Purpose
Postnatal Depression, Depression, Postpartum
Status
Completed
Phase
Phase 2
Locations
Pakistan
Study Type
Interventional
Intervention
Complex Intervention
Sponsored by
About this trial
This is an interventional treatment trial for Postnatal Depression focused on measuring Postnatal depression, Maternal depression, Psychosocial intervention
Eligibility Criteria
Inclusion Criteria:
- Depressed mothers over the age of 18 years
- Having one or more infants 6-18 months old
- Ability to give informed consent
- Resident in the study catchment area
Exclusion Criteria:
- Women or child with diagnosed physical or learning disability and women having post-partum or other psychosis
Sites / Locations
- Civil hospital
- Abbasi Shaheed hospital Karachi
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Complex Intervention (LTP-TH)
Control group
Arm Description
The 12 sessions of complex intervention (LTP-TH) will be delivered to mothers.
Control group will receive standard postnatal follow-up.
Outcomes
Primary Outcome Measures
Depression
We will measure change from baseline in symptoms of depression through Hamilton Depression Rating Scale (HDRS) at six months by using 17 item HDRS.
Postnatal Depression
Edinburgh Postnatal Depression Scale (EPDS) will be used to identify mothers with postnatal depression.
Secondary Outcome Measures
Infants' weight
Will be measured through standard anthropometric techniques and equipments
Infants' height
Will be measured through standard anthropometric techniques and equipments
Social Support
Social support of participants will be measured with OSLO 3-Items Social Support Scale
health related quality of life
EuroQol-5D(EQ-5 D) will be used to measures health related quality of life in five dimensions. It provides a simple descriptive profile and a single index value for health status.
Maternal Attachment
Maternal attachment with infants will be measured with Maternal Attachment Inventory (MAI)
Full Information
NCT ID
NCT01309516
First Posted
January 22, 2011
Last Updated
September 19, 2015
Sponsor
Pakistan Institute of Living and Learning
Collaborators
Dow University of Health Sciences, University of Manchester
1. Study Identification
Unique Protocol Identification Number
NCT01309516
Brief Title
Randomised Control Trial of a Complex Intervention for Postnatal Depression
Official Title
Efficacy of Learning Through Play Plus Intervention to Reduce Maternal Depression for Women With Under-nourished Children: A Randomized Controlled Trial From Pakistan
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
May 2009 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
May 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pakistan Institute of Living and Learning
Collaborators
Dow University of Health Sciences, University of Manchester
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study aims to:
Develop a culturally appropriate psychosocial intervention
Test feasibility and acceptability of psychosocial intervention in women suffering from postnatal depression.
Primary Hypothesis:
Depressed mothers who will receive the group intervention will show significant improvements in terms of symptoms of depression.
Design:
Randomised controlled trial.
Setting:
Outpatient department of Civil hospital Karachi.
Participants:
A total of 84 depressed mothers will be randomised equally to an intervention group and a Treatment as usual control group.
Interventions:
The 12 session multimodal psychosocial intervention will be delivered to mothers in the intervention group over a three months period. Each session would take up to 45 minutes. Control group will receive standard postnatal follow-up.
Outcome measures:
Primary outcome measures would be mothers' scores on Edinburgh Postnatal Depression Scale (EPDS)and Hamilton Depression Rating Scale (HDRS).
Detailed Description
A number of individual and group interventions targeting maternal depression have been developed and tested, mostly in developed countries. Group-based approaches have usually been used to improve outcomes in children through parent-training programmes. A meta-analysis of such programmes shows that these can also be effective in improving psychosocial and mental health of the mothers. However, a number of health system and cultural differences make it difficult for mental health interventions to be extrapolated from the developed to the developing world.
Design:
The interventions will be assessed using a prospective randomised controlled design, using two groups: psychosocial group therapy (Learning Through Play + principles of Cognitive Behaviour Therapy)and treatment as usual.
Defining the intervention:
The intervention will include a supportive component, an educational component, and practical advice on using health services, a parenting component, and a psychosocial component. The objective will be to help mothers feel supported, empowered and confident about their parenting abilities, which in turn may help to reduce their level of depression. Further qualitative testing of the intervention will take place to refine the manualized intervention.
Psychiatric Measures:
The level of severity of depression will be assessed using the Edinburgh Postnatal Depression Scale (EPDS) (Cox and Holden, 1994) and the Hamilton Depression Rating Scale (HDRS) (Hamilton, 1960).
Women scoring 12 or over on the EPDS and 13 or over on the HDRS will be asked to undergo a diagnostic interview using the Clinical Interview Schedule-Revised (CIS-R).
To measure mother infant attachment the Maternal Attachment Inventory (Muller, 1994) will be used.
OSLO-3 item Social Support Scale (Dalgard, 1996) will be used to measure social support.
The adapted Verona Service Satisfaction Scale (Tansella, 1991) will be used to measure patient satisfaction with support and treatment.
Quality of life will be measured by using the EuroQol-5D (EQ-5D).
The qualitative interviews will be used to elicit information about previous attempts for help with mental health issues and questions regarding participants understanding of their postnatal depression and their future expectations from a perinatal service.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postnatal Depression, Depression, Postpartum
Keywords
Postnatal depression, Maternal depression, Psychosocial intervention
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
107 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Complex Intervention (LTP-TH)
Arm Type
Experimental
Arm Description
The 12 sessions of complex intervention (LTP-TH) will be delivered to mothers.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Control group will receive standard postnatal follow-up.
Intervention Type
Behavioral
Intervention Name(s)
Complex Intervention
Other Intervention Name(s)
Multimodal Psychosocial Intervention
Intervention Description
This 12 session Multimodal Psychosocial Intervention will include a supportive component, an educational component, psychosocial component and a parenting programme.
Primary Outcome Measure Information:
Title
Depression
Description
We will measure change from baseline in symptoms of depression through Hamilton Depression Rating Scale (HDRS) at six months by using 17 item HDRS.
Time Frame
6 months
Title
Postnatal Depression
Description
Edinburgh Postnatal Depression Scale (EPDS) will be used to identify mothers with postnatal depression.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Infants' weight
Description
Will be measured through standard anthropometric techniques and equipments
Time Frame
6 months
Title
Infants' height
Description
Will be measured through standard anthropometric techniques and equipments
Time Frame
6 months
Title
Social Support
Description
Social support of participants will be measured with OSLO 3-Items Social Support Scale
Time Frame
6 months
Title
health related quality of life
Description
EuroQol-5D(EQ-5 D) will be used to measures health related quality of life in five dimensions. It provides a simple descriptive profile and a single index value for health status.
Time Frame
6 months
Title
Maternal Attachment
Description
Maternal attachment with infants will be measured with Maternal Attachment Inventory (MAI)
Time Frame
6 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Depressed mothers over the age of 18 years
Having one or more infants 6-18 months old
Ability to give informed consent
Resident in the study catchment area
Exclusion Criteria:
Women or child with diagnosed physical or learning disability and women having post-partum or other psychosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nusrat Husain, MD
Organizational Affiliation
University of Manchester
Official's Role
Principal Investigator
Facility Information:
Facility Name
Civil hospital
City
Karachi
State/Province
Sindh
ZIP/Postal Code
75600
Country
Pakistan
Facility Name
Abbasi Shaheed hospital Karachi
City
Karachi
State/Province
Sindh
Country
Pakistan
12. IPD Sharing Statement
Links:
URL
http://pill.org.pk
Description
Pakistan Institute of Learning & Living, Organization (Collaborator) offering logistic and technical support.
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Randomised Control Trial of a Complex Intervention for Postnatal Depression
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