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Clinical Trials/NCT01309516
NCT01309516
Completed
Phase 2

Efficacy of Learning Through Play Plus Intervention to Reduce Maternal Depression for Women With Under-nourished Children: A Randomized Controlled Trial From Pakistan

Pakistan Institute of Living and Learning2 sites in 1 country107 target enrollmentMay 2009

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Postnatal Depression
Sponsor
Pakistan Institute of Living and Learning
Enrollment
107
Locations
2
Primary Endpoint
Depression
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The study aims to:

  1. Develop a culturally appropriate psychosocial intervention
  2. 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.

Registry
clinicaltrials.gov
Start Date
May 2009
End Date
May 2011
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

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

Outcomes

Primary Outcomes

Depression

Time Frame: 6 months

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

Time Frame: 6 months

Edinburgh Postnatal Depression Scale (EPDS) will be used to identify mothers with postnatal depression.

Secondary Outcomes

  • Maternal Attachment(6 months)
  • Infants' weight(6 months)
  • Infants' height(6 months)
  • Social Support(6 months)
  • health related quality of life(6 months)

Study Sites (2)

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