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Maternal Well-being in the Postnatal Stage

Study acronym: BIEMAT
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated May 21, 2025 (before its estimated June 1, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Notable Primary completion date: Jun 2024 to Jun 1, 2025
    • Study completion date: Jun 2024 to Mar 1, 2026
    v4
  2. Minor Interventions: positive psychology intervention (Behavioral) to Cognitive Behavior Therapy (Behavioral), Positive Psychology Intervention (Behavioral)
    • Secondary endpoints: 7 to 6
    • Study description expanded, about 26 words
    v3
  3. Notable Primary completion date: Apr 2023 to Jun 2024v2 Show 4 more changesShow less
    • Interventions: Intervention in positive psychology (Behavioral) to positive psychology intervention (Behavioral)
    • Secondary endpoints revised (7)
    • Study description expanded, about 205 words
    • Site contact updated
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The objective of this study is to design and validate an online intervention aimed at promoting well-being in women with postpartum depression. For this, the design of a multicomponent protocol consisting of empirically validated positive interventions and comparing these with a group Cognitive Behavioral Therapy (CBT) is proposed, following the National Institute for Health and Care Excellence (NICE) recommendations for the treatment of depression. Participants will be screened for inclusion in the program if they meet clinical criteria. After that, they will be randomly assigned to a CBT group or a positive psychology intervention (PPI) group.
Trial Details
NCT Number NCT05676918
Lead Sponsor Universidad Complutense de Madrid
Collaborators: Universidad Pontificia de Salamanca
Conditions
(from sponsor)
Postpartum Depression, Postpartum Disorder
Related terms Depression, Postpartum, Puerperal Disorders
Enrollment 98 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov