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Life sciences · Observational Study
ClinicalTrials.gov · September 17, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Observational Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07382336). This is a study registration, not published results. Lead sponsor: The Hong Kong Polytechnic University. Recruitment status: COMPLETED. Study type: OBSERVATIONAL. Enrollment: 120 participants (ACTUAL). Conditions: Postpartum Depression (PPD). Interventions: DIAGNOSTIC_TEST: Ecological momentary assessment and retrospective assessment. Primary outcome measures: Ecological Momentary Questions (Mood) , Three momentary assessments per day for five days in each month for 6 months, displayed randomly within each of the following intervals: 0900-1300, 1300-1800 and 1800-0000.; Edinburgh Postnatal Depression Scale (EPDS) , At the baseline and the end of each of the 6 months in the period.. Brief summary: This pilot study will recruit 120 perinatal pregnant women and follow them up for 6 months. Both momentary and retrospective assessments of emotional well-being and psychosocial factors will be conducted on a mobile application. We aim to understand the symptom trajectories and provide evidence for effective individualized interventions.