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Trial · NCT03022526

Registered outcomes15

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryEdinburgh Postnatal Depression Score (EPDS)6 weeks
Self-completed questionnaire, electronically completed. Scores range from 0-30, with higher score indicating higher likelihood of depressive illness. A score of 10 or greater is characterized as possible depression.
SecondaryPain Score on Average (BPI - Short Form)2 days postpartum
Self-completed questionnaire, electronically completed. Pain scores range from 0 (no pain) to 10 (pain as bad as you can imagine). Participants only answered this question if answered "yes" to question: "Have you had pain other than everyday kinds of pain today?"
SecondaryPain Score on Average (BPI - Short Form)6 weeks postpartum
Self-completed questionnaire, electronically completed. Pain scores range from 0 (no pain) to 10 (pain as bad as you can imagine). Participants only answered this question if answered "yes" to question: "Have you had pain other than everyday kinds of pain today?"
SecondaryPain Score on Average (BPI - Short Form)3 months postpartum
Self-completed questionnaire, electronically completed. Pain scores range from 0 (no pain) to 10 (pain as bad as you can imagine). Participants only answered this question if answered "yes" to question: "Have you had pain other than everyday kinds of pain today?"
SecondaryPerceived Stress (PSS)2 days postpartumSelf-completed questionnaire, electronically completed. Scores range from 0-40, with higher scores indicating higher perceived stress.
SecondaryNumber of Participants Currently Breastfeeding at 2 Days Postpartum (Yes/No)2 Days PostpartumSelf-completed questionnaire, electronically completed. Results represent the percentage of each arm currently breastfeeding at this time point.
SecondaryNumber of Participants Currently Breastfeeding at 6 Weeks Postpartum (Yes/No)6 weeks postpartumSelf-completed questionnaire, electronically completed. Results represent the percentage of each arm currently breastfeeding at this time point.
SecondaryNumber of Participants Currently Breastfeeding at 3 Months Postpartum (Yes/No)3 months postpartumSelf-completed questionnaire, electronically completed. Results represent the percentage of each arm currently breastfeeding at this time point.
SecondaryParent-Infant Attachment (MPAS)6 weeks postpartumSelf-completed questionnaire, electronically completed. Scores range from 19-95, with higher scores indicating higher attachment.
SecondaryParent-Infant Attachment (MPAS)3 months postpartumSelf-completed questionnaire, electronically completed. Scores range from 19-95, with higher scores indicating higher attachment.
SecondaryChild Development (ASQ-3) Personal Social Score6 weeks postpartumSelf-completed questionnaire, electronically completed. Scores range from 0-60, with higher scores indicating higher personal-social development.
SecondaryChild Development (ASQ-3) Personal Social Score3 months postpartumSelf-completed questionnaire, electronically completed. Scores range from 0-60, with higher scores indicating higher personal-social development.
SecondaryParenting Self-efficacy (PMP-SE)6 weeks postpartumSelf-completed questionnaire, electronically completed. Scores range from 20-80, with higher scores indicating higher parenting self-efficacy.
SecondaryParenting Self-Efficacy (PMP-SE)3 months postpartumSelf-completed questionnaire, electronically completed. Scores range from 20-80, with higher scores indicating higher parenting self-efficacy.
SecondaryEdinburgh Postnatal Depression Score (EPDS)3 months
Self-completed questionnaire, electronically completed. Scores range from 0-30, with higher score indicating higher likelihood of depressive illness. A score of 10 or greater is characterized as possible depression.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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