WhatsApp-based intervention for pregnant women and their partners to improve psychological well-being and sleep quality
Official title: WhatsApp-based Psycho-socio-educational Intervention (WeLove) for Prevention of Psychological and Sleep Problems in Pregnant Women and Their Partners: A Three-arm Double-blinded Pilot Randomised Controlled Trial
Run by Chinese University of Hong Kong · NCT06768190 · Data updated 2026-11-12
This study is testing a WhatsApp program designed to help pregnant women and their partners improve their mental health and sleep quality.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | January 6, 2025 |
| Main results expected | January 31, 2026 |
| Study ends | January 31, 2027 |
| Registry record updated | January 23, 2025 |
| Trial ID | NCT06768190 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are pregnant women between 12 to 28 weeks of gestation and their partners who can read and understand Chinese.
✕Probably not a fit
Patients with current severe medical illnesses or existing psychological and sleep disorders may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This pilot randomized controlled trial evaluates the feasibility and acceptability of a WhatsApp-based psycho-socio-educational intervention called WeLove, aimed at preventing psychological and sleep problems in pregnant women and their partners. The study involves 60 couples who will be randomly assigned to one of three groups: the WeLove intervention for couples, the WeLove intervention for pregnant women only, or a control group using WhatsApp as usual. The intervention consists of six sessions that include psychological, social, and educational components, followed by individual interviews for process evaluation. The study aims to preliminarily assess the effects of the intervention on psychological symptoms, sleep quality, and life satisfaction.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the psychological well-being and sleep quality of pregnant women and their partners.
How similar studies have gone: While the specific approach of using WhatsApp for psycho-socio-educational interventions is relatively novel, similar studies have shown promise in improving psychological outcomes through digital platforms.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * current severe medical illnesses * psychological and sleep disorders
Where it's running
-
The Chinese University of Hong Kong
Hong Kong, Hong Kong Recruiting
Study contacts
- Study coordinator: Ying Lau, PhD
- Email: yinglau@cuhk.edu.hk
- Phone: (852) 39436222
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Nature-based program feasibility in preschools near public housing
This feasibility study tests whether a nature-based program in preschools near public housing can be run smoothly and whether families will participate and benefit.
-
Relaxation audio during breastfeeding to help newborn growth and mom’s well-being
Researchers will test if listening to a relaxation audio during breastfeeding helps LBW babies grow and reduces maternal stress in a Ugandan setting.
-
AI chatbot for improving sleep in adults
A chatbot-based AI sleep program is being tested to see if it helps adults with sleep problems sleep better.
-
Mindfulness for Emotional Distress: An EEG-Based Trial in Adults
A randomized trial tests a mindfulness program for adults with subclinical emotional distress to see if it reduces anxiety and changes brain activity compared with progressive muscle relaxation.
-
Sleep problems before heart surgery may affect recovery outcomes
This study tests whether preoperative sleep issues in adults undergoing cardiac surgery are linked to different perioperative metabolites and postoperative outcomes.
-
Mindfulness-Based Stress Reduction Program for nursing students
This trial tests whether a Mindfulness-Based Stress Reduction program can help nursing students reduce stress and improve mood and well-being.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.