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Effect of 'Parentbot - a Digital Healthcare Assistant (PDA)' in Improving Parenting Outcomes During the Perinatal Period

Effectiveness of 'Parentbot - a Digital Healthcare Assistant (PDA)', a Mobile Application-based Intervention, in Improving Parental Psychosocial Outcomes During the Perinatal Period: a Randomized Controlled Trial and Process Evaluation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05463926
Acronym
PDA
Enrollment
236
Registered
2022-07-19
Start date
2022-11-15
Completion date
2023-08-31
Last updated
2024-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Parenting Satisfaction, Parents, Perinatal Depression, Self Efficacy, Stress

Brief summary

The Parentbot - a Digital healthcare Assistant (PDA) is a mobile application-based psychosocial parenting intervention with integrated chatbot features, intended for couples to use during the perinatal period. It provides parents with multimedia educational materials (text files, audio files and videos), discussion forum, guided mindfulness-based meditation videos, guided reflection and gratitude journals and a chatbot to answer their queries related to perinatal care in real-time. This study aims to: 1. Develop a theory-based perinatal intervention with integrated chatbot features for both first-time and experienced parents 2. Examine the effectiveness of the PDA intervention in improving parenting self-efficacy (primary outcome), stress, depression, anxiety, social support, parent-child bonding and parenting satisfaction (secondary outcomes) among parents during the perinatal period 3. Examine the perceptions of parents from both the intervention and control group after the intervention 4. Collate suggestions for further improvement from the participants and members of the research team The hypotheses of this study are: The PDA intervention group will have significantly higher scores for parenting self-efficacy, social support, parent-child bonding and parenting satisfaction, as well as lower scores for stress, depression and anxiety compared to the control group receiving standard care after the intervention at one-month postpartum (post-test 1) and three-months postpartum (post-test 2).

Interventions

BEHAVIORALPDA mobile application

Parentbot - a Digital healthcare Assistant (PDA): A mobile application-based psychosocial parenting intervention with integrated chatbot features. It consists of multimedia educational materials (text files, audio files and videos), discussion forums, guided mindfulness-based meditation videos, guided reflection and gratitude journals and a chatbot.

Sponsors

National University of Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Two-group parallel-armed randomized controlled trial (RCT) with a pretest and repeated posttest experimental design

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Heterosexual married couples who are first-time parents or experienced parents are included if they: * Are at least 21 years old * Are fluent in English * Own a smartphone with internet access * Intend to stay in Singapore until three months postpartum * Are having a low-risk singleton or multiple pregnancy at \> 24 gestational weeks (age of viability).

Exclusion criteria

Couples will be excluded if either parent has: * Any self-reported psychiatric disorders, visual, auditory, cognitive impairment and/or any major medical condition that can affect their abilities to participate in the trial * High-risk pregnancy including placenta previa major, pre-eclampsia, intrauterine growth restriction etc * Suffer from a miscarriage or made the decision to abort their child * Give birth to still-birth newborn * Give birth to a newborn with congenital anomalies or medical complications (require intensive care, severe jaundice, Down's syndrome) Single parents will also be excluded. If either the mother or father declines to participate in the study while their partner agrees, the couple will not be allowed to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Parenting self-efficacy1 month postpartum10-item Parenting Efficacy Scale (PES): Score ranges from 10-40, with higher scores indicating a higher level of perceived parenting self-efficacy

Secondary

MeasureTime frameDescription
Depression1 month postpartum10-item Edinburgh Postnatal Depression Scale (EPDS) Scale: Score ranges from 0-30, with higher scores indicating more severe depressive symptoms
Anxiety1 month postpartum40-item State-Trait Anxiety Inventory (STAI): Score ranges from 40-160, with higher scores indicating more severe anxiety symptoms
Stress1 month postpartum10-item Perceived Stress Scale (PSS): Score ranges from 0-40, with higher scores indicating higher stress levels
Parent-child bonding1 month postpartum8-item Parent-Infant Bonding Questionnaire (PIBQ): Score ranges from 0-24, with higher scores indicating poorer parent-child bonding
Parenting satisfaction1 month postpartum11-item evaluation subscale of the What Being the Parent of a Baby is Like scale (WBPL): Score ranges from 0-90, with higher scores indicating greater parenting satisfaction
Social support1 month postpartum4-item Perceived Social Support for Parenting scale (PSSP): Score ranges from 0-16, with higher scores indicating higher level of perceived social support

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026