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Randomised Control Trial of a Complex Intervention for Postnatal Depression

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01309516
Enrollment
107
Registered
2011-03-07
Start date
2009-05-31
Completion date
2011-05-31
Last updated
2015-09-22

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

Conditions

Depression, Postpartum, Postnatal Depression

Keywords

Postnatal depression, Maternal depression, Psychosocial intervention

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.

Interventions

This 12 session Multimodal Psychosocial Intervention will include a supportive component, an educational component, psychosocial component and a parenting programme.

Sponsors

Dow University of Health Sciences
CollaboratorOTHER
University of Manchester
CollaboratorOTHER
Pakistan Institute of Living and Learning
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Depression6 monthsWe will measure change from baseline in symptoms of depression through Hamilton Depression Rating Scale (HDRS) at six months by using 17 item HDRS.
Postnatal Depression6 monthsEdinburgh Postnatal Depression Scale (EPDS) will be used to identify mothers with postnatal depression.

Secondary

MeasureTime frameDescription
Social Support6 monthsSocial support of participants will be measured with OSLO 3-Items Social Support Scale
Infants' weight6 monthsWill be measured through standard anthropometric techniques and equipments
Maternal Attachment6 monthsMaternal attachment with infants will be measured with Maternal Attachment Inventory (MAI)
health related quality of life6 monthsEuroQol-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.
Infants' height6 monthsWill be measured through standard anthropometric techniques and equipments

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026