Clinical Trial

Pregnancy Care Digital Intervention for Maternal Anxiety in the Third Trimester (PCYCARE-RCT)

Study acronym: PCYCARE-RCT
Completed
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Summary
The goal of this clinical trial is to evaluate whether a digital self-care intervention (PCYCARE) can reduce pregnancy-related anxiety and improve biopsychosocial adaptation among third-trimester pregnant women. The main questions it aims to answer are: 1. Does the PCYCARE digital program reduce pregnancy-related anxiety in third-trimester pregnant women? 2. Does the intervention improve maternal knowledge, childbirth preparedness, and sleep quality? Researchers will compare participants who receive the PCYCARE digital program with those who receive routine antenatal care to determine the effectiveness of the intervention. Participants will: 1. Use the PCYCARE mobile-based program for 21 days, which includes educational modules and guided audio relaxation sessions 2. Complete two sessions per day (education and relaxation), each lasting approximately 10-15 minutes 3. Complete questionnaires at baseline and after the intervention to assess anxiety, sleep quality, maternal knowledge, and childbirth preparedness
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-11-14; most recent amendment 2026-04-01.
Status change: Active, Not Recruiting → Completed 2026-01-12
Trial Details
NCT Number NCT07229989
Lead Sponsor Lincoln University College Malaysia
Conditions Pregnancy-Related Anxiety (PrA), Anxiety
Enrollment 120 participants
Start Date 2025-09-18
Primary Completion 2025-09-20 (estimated)
Study Completion 2025-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-04-07