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Clinical Trials/ISRCTN14864807
ISRCTN14864807
Active, not recruiting
未知

Evaluation of telephone-based peer-support intervention programme for preventing postnatal depression: a randomized controlled trial

ational University of Singapore0 sites138 target enrollmentJuly 25, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Postnatal depression
Sponsor
ational University of Singapore
Enrollment
138
Status
Active, not recruiting
Last Updated
6 years ago

Overview

Brief Summary

  1. 2018 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/29540338 2. 2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/31469084 (added 02/09/2019) 3. 2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/31469080 (added 02/09/2019)
Registry
who.int
Start Date
July 25, 2017
End Date
February 28, 2020
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
ational University of Singapore

Eligibility Criteria

Inclusion Criteria

  • The inclusion criteria for participants are mothers who:
  • 1\. Are 21 years old and above
  • 2\. Are able to read and speak English
  • 3\. Owns a telephone and willing to share her number
  • 4\. Plan to stay in Singapore for first three months post birth of their newborns
  • The inclusion criteria for the peer volunteers are mothers who:
  • 1\. Are 21 years old and above
  • 2\. Are able to read and speak English
  • 3\. Have delivered a healthy baby in the past
  • 4\. Self\-reported history of and recovery from PND

Exclusion Criteria

  • The exclusion criteria for the participants are mothers who:
  • 1\. Have physical or mental disorders which would interfere with their ability to participate in the study
  • 2\. Have complicated assisted delivery such as vacuum or forceps with 4th degree perineal tear of the mother
  • 3\. Give birth to a newborn at stillbirth or a newborn with congenital anomalies and/or medical complications
  • The exclusion criteria for the peer volunteers:
  • 1\. Have physical or mental disorders which would interfere with their ability to participate in the study
  • 2\. Does not want to share their number and call needy mothers as instructed by research team

Outcomes

Primary Outcomes

Not specified

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