Actively Recruiting
Integrating Smart Ring Wearable Technology in Pregnancy Health Monitoring (I-SMART)
Led by KK Women's and Children's Hospital · Updated on 2025-04-25
100
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to test the following hypotheses in a single-arm observational study in 70-100 healthy pregnant multi-ethnic women who will be followed-up from the first trimester of pregnancy to the third trimester of pregnancy. Aim 1: To assess the applicability, acceptability and compliance with the use of a wearable smart ring together with smart digital devices (e.g., smart phone) during pregnancy. Hypothesis 1: The investigators hypothesize that participants will respond favorably to the use of the smart ring to monitor their physical activity and sleep during pregnancy. Aim 2: To assess the association between maternal characteristics (age, pre-pregnancy BMI, pregnancy weight gain, stress, anxiety and depression symptoms) with physical activity markers (energy expenditure, and step count) and sleep markers (duration, quality, sleep onset latency, wake after sleep onset, time in bed and heart rate variability) collected from the smart ring in the second trimester of pregnancy. Hypothesis 2: The investigators hypothesize that specific maternal characteristics will be associated with physical activity markers (energy expenditure, and step count), as well as sleep markers (duration, quality, sleep onset latency, wake after sleep onset, time in bed and heart rate variability).
CONDITIONS
Official Title
Integrating Smart Ring Wearable Technology in Pregnancy Health Monitoring (I-SMART)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women from the first to third trimester (4-39 weeks of gestation)
- Mobile phone operating system supported by the smart ring application
- Aged 21 years and above
You will not qualify if you...
- Cannot read or speak English
- Below 21 years of age
- Gestational age below 4 weeks or above 39 weeks
- Limited mobility
- Diagnosed with severe unstable mental conditions
- Diagnosed with severe chronic disorders
- Mobile device not compatible with the smart ring
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
KK Women's and Children's Hospital
Singapore, Singapore, 229899
Actively Recruiting
Research Team
K
Kok Hian Tan, MD
CONTACT
P
Phaik Ling, Elaine Quah, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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