Cultivation of Mindfulness Via Instant Messaging to Promote Parental Wellbeing and Supportive Parenting

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Completed
CT.gov ID
NCT05413577
Collaborator
(none)
564
1
2
5.9
95.4

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness training
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
564 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Cultivation of Mindfulness Via Instant Messaging to Promote Parental Wellbeing and Supportive Parenting
Actual Study Start Date :
Sep 1, 2021
Actual Primary Completion Date :
Feb 28, 2022
Actual Study Completion Date :
Feb 28, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Group

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.

Behavioral: Mindfulness training
The intervention recordings taught the basic concepts of mindfulness through simple guided meditations with content supported by science. Each recording had the same format that included (1) a daily theme, (2) a meditation exercise echoing the theme, (3) a suggested exercise for practice, and (4) an invitation for participants to give a short response to their meditation experience at the end of the recording.

No Intervention: Waitlist control group

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.

Outcome Measures

Primary Outcome Measures

  1. Parental Stress Scale [Change from Baseline Parental Stress Scale at immediately after the intervention and two weeks after intervention]

    The Parental Stress Scale was used to measure self-perceived stress specific to the parenting role. Parental Stress Scale was originally developed by Berry and Jones (1995) to measure parental feelings and experiences in terms of rewards, satisfaction, controllability, and stress. The minimum score was 0 and the maximum score was 64. A score of 0 represents lowest level of parental stress possible, whereas a score of 64 represents highest level of parental stress. Higher scores indicate worse outcome.

  2. Mindfulness in Parenting Scale [Change from Baseline Interpersonal Mindfulness in Parenting scale at immediately after the intervention and two weeks after intervention]

    The 31-item Interpersonal Mindfulness in Parenting scale was adopted to measure parents' self-reported engagement in mindful parenting (Duncan, 2007). The minimum score was 0 and the maximum score was 155. A score of 0 represents lowest level of parental mindfulness, whereas a score of 155 represents highest level of parental mindfulness possible. Higher scores indicate better outcome.

  3. Parent Behavior Inventory [Change from Baseline Parent Behavior Inventory at immediately after the intervention and two weeks after intervention]

    The Parent Behavior Inventory was used to assess the change in parenting behavior before and after the intervention. The Parent Behavior Inventory has two independent scales, supportive/engaged and hostile/coercive parenting (Lovejoy et al., 1999), The minimum score was 0 and the maximum score for each scale was 50. A score of 0 represents lowest frequency of parenting behaviors on supportive/engaged and hostile/coercive parenting, whereas a score of 50 represents highest frequency of supportive/engaged and hostile/coercive parenting possible. Higher scores of supportive/engaged scale indicate better outcome. Lower scores of hostile/coercive scale indicate better outcome.

Secondary Outcome Measures

  1. Well-being WHO 5-item index [Change from Baseline Well-being WHO 5-item index at immediately after the intervention and two weeks after intervention]

    Global mental well-being was measured using the Well-being WHO 5-item index (Topp et al., 2015).The minimum score was 0 and the maximum score was 25. A score of 0 represents worst possible, whereas a score of 25 represents best possible quality of life. Higher scores indicate better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chinese University of Hong Kong Shatin Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Lun Wai Doris Lam, M.S.Sc, Chinese University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lam Lun Wai Doris, Principal Investigator, Graduate Student in Clinical Psychology, Department of Psychology, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05413577
Other Study ID Numbers:
  • SBRE-20-562
First Posted:
Jun 10, 2022
Last Update Posted:
Jun 10, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 10, 2022