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Behavioural Interventions for Postnatal Depression: a RCT Study

Not Applicable
Completed
Conditions
Postnatal Depression
Registration Number
NCT03196726
Lead Sponsor
Ministry of Health, Malaysia
Brief Summary

Randomized-controlled trial on the effectiveness of managing postnatal depression mothers at primary care clinics using Cognitive-behavioural therapy treatment by nurses as adjunct to management by Medical Officer as compared to Medical Officer alone

Detailed Description

This was a two-group double-blind randomized controlled trial (RCT) conducted in six primary care clinics at Klang Valley, with 27 subjects in each arms. All post-partum women at 4 to 24 weeks, registered at these clinics, were screened using self-administered Edinburgh Postnatal Depression Scale for symptoms of depression. Those who scored 12 or more and/or positive for question on suicidal behaviour, were interviewed by trained Research Assistants using Mini International Neuropsychiatric Interview, a diagnostic interview tool. Those with mild to moderate depression were invited to join this study, while severe depressed cases were referred to the Family Medicine Specialist for appropriate management. Consented eligible women were randomized into either control group; managed by Medical Officers alone, or intervention group; managed by both Medical Officers and trained nurses. Medical officers were given standard refresher course on Postnatal Depression management based on Clinical Practice Guideline while nurses were trained using brief cognitive-behavioural therapy (CBT) module, which consists of 6 modules for 6 weekly sessions. Depression level and its severity were assessed using self-administered Beck's Depression Index (BDI) and Automatic Thought Questionnaire (ATQ), at Baseline, Week 3 and Week 6.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
54
Inclusion Criteria
  • postpartum 4-24 weeks
  • registered with selected primary care clinics
  • Edinburgh Postnatal Depression score: 12 or more; and Mini diagnostic interview:

positive (mild to moderate depression)

  • consented to participate
Exclusion Criteria
  • severe depression or psychosis

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
changes in depression levelat baseline (Week 0), week 3 and Week 6

assess changes in Beck Depression Index (BDI) score

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (6)

Klinik Kesihatan Seksyen 7,

🇲🇾

Shah Alam, Selangor, Malaysia

Klinik Kesihatan Kuala Lumpur

🇲🇾

Kuala Lumpur, W.P. Kuala Lumpur, Malaysia

Klinik Kesihatan Sg Besi

🇲🇾

Kuala Lumpur, WP Kuala Lumpur, Malaysia

Klinik Kesihatan Presint 11

🇲🇾

Putrajaya, WP Putrajaya, Malaysia

Klinik Kesihatan Presint 9

🇲🇾

Putrajaya, WP Putrajaya, Malaysia

Klinik Kesihatan Presint 18

🇲🇾

Putrajaya, WP Putraya, Malaysia

Klinik Kesihatan Seksyen 7,
🇲🇾Shah Alam, Selangor, Malaysia

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