About this trial
Objectives: (1) evaluate the feasibility and acceptability of the WhatsApp-based psycho-socio-educational intervention (WeLove); (2) preliminarily examine the effects of the intervention on psychological symptoms (depression, anxiety, stress symptoms), sleep quality, and life satisfaction; and (3) preliminarily examine the interdependence between psychological symptoms and sleep quality in pregnant women and their partners.
Methods: The investigators will use WhatsApp to provide the six sessions of the intervention, which include psychological, social, and educational components. A three-arm double-blinded pilot randomised controlled trial (RCT) is used in 60 couples, followed by individual face-to-face interviews for process evaluation in 10 to 20 couples based on data saturation. Participants will be assigned to one of three groups and 20 couples per group: intervention 1 (couples for WeLove), intervention 2 (pregnant women for WeLove), or the control group (use WhatsApp as normal). Participants will be assessed pre- and post-intervention. Generalised estimating equation analysis and thematic analysis will be performed to examine the research objectives.
Eligibility criteria
Qualifiers
pregnant with a gestation of >12 to 28 weeks and their partners over 18 years
able to read and understand Chinese
have electronic devices with WhatsApp that can contact the Internet
can provide written consent and voluntary participation in this study
Disqualifiers
current severe medical illnesses
psychological and sleep disorders
Trial design
Treatments tested in this trial
- WhatsApp as usual
- WhatsApp-based psycho-socio-educational intervention (WeLove)
Treatment groups
Sponsors and collaborators
Chinese University of Hong Kong
Lead sponsor
Hospital Authority, Hong Kong
Collaborator