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Reducing Parental Stress Via Instant Messaging During COVID-19 Pandemic: A Randomized Controlled Trial

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Completed

Conditions

Parenting
Parents
Stress

Treatments

Behavioral: Mindfulness training

Study type

Interventional

Funder types

Other

Identifiers

NCT05413577
SBRE-20-562

Details and patient eligibility

About

This research investigated the effects of mindfulness practice on mental wellbeing and parenting behaviour, with the instruction recordings delivered via existing instant messaging applications, including Whatsapp and Signal. The two-week mindfulness program targeted parents with children in Nursery, Kindergarten to Primary School. Due to the suspension of schools, work from home policies, parents spend increased amount of time with their children. News reports have indicated that with the mounting care taking responsibilities and downturn of economy amidst the epidemic, parents have been experiencing higher stress that may negatively impact their wellbeing and parent-child relationship. This study delivered an app-based intervention that aims at enhancing mindful parenting at the time of corona, where social distancing is emphasized.

Enrollment

491 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Parents with at least one child who is in Primary School or below.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

491 participants in 2 patient groups

Experimental Group
Experimental group
Description:
The experimental group was invited to listen to a 15-minute mindfulness instructional recording delivered daily through an instant messaging application and to practice accordingly for 14 consecutive days at their own choice of time and place.
Treatment:
Behavioral: Mindfulness training
Waitlist control group
No Intervention group
Description:
The waitlist control group was only be required to complete the demographic information, pre, post experiment and follow-up questionnaires before they receive the mindfulness training intervention.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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