NCT04875507

Brief Summary

Positive psychology interventions use positive psychology techniques to identify meaning and value in life events to raise positive feelings and emotions. Application of PPIs has steadily increased in clinical and non-clinical samples. However, that meta-analysis did not include any study in a Chinese population, and it remains unclear whether PPIs are applicable in the Hong Kong Chinese context.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2021

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 20, 2021

Completed
16 days until next milestone

First Posted

Study publicly available on registry

May 6, 2021

Completed
7 months until next milestone

Study Start

First participant enrolled

December 1, 2021

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2023

Completed
Last Updated

April 19, 2022

Status Verified

April 1, 2022

Enrollment Period

1.7 years

First QC Date

April 20, 2021

Last Update Submit

April 12, 2022

Conditions

Keywords

PovertyPositive PsychologyDepressive symptomsSelf-esteemQuality of life

Outcome Measures

Primary Outcomes (19)

  • Screening rate

    The number of children screened by the RA divided by the number of children available for screening during the recruitment period.

    At baseline

  • Eligibility rate

    The number of eligible children divided by the number of screened children

    At baseline

  • Consent rate

    The number of eligible children who consent to participate divided by the number of eligible children

    At baseline

  • Randomization rate

    The number of children randomized to the experimental and control groups divided by the number of consenting children

    At baseline

  • Intervention attendance rate

    The number of participants in the experimental group who complete the intervention divided by the number of participants randomized into the group

    Immediately after the training workshop

  • Intervention attendance rate at 1-week follow-up

    The number of participants in the experimental group who complete the intervention divided by the number of participants randomized into the group

    At 1-week follow-up

  • Adherence to the intervention protocol at 1-week follow-up

    The number of participants in the experimental group who practice the skills gained divided by the number of participants randomized into the group

    At 1-week follow-up

  • Retention rate at 6-month follow-up

    The number of participants who remain in this study divided by the number of randomized participants, calculated by group at each follow-up

    At 6-month follow-up

  • Completion rate at 6-month follow-up

    The number of participants who return the questionnaires divided by the number of questionnaires distributed

    At 6-month follow-up

  • Missing data at baseline

    The percentage of missing in the dataset

    At baseline

  • Missing data at 1-week follow-up

    The percentage of missing in the dataset

    At 1-week follow-up

  • Missing data at 1-month follow-up

    The percentage of missing in the dataset

    At 1-month follow-up

  • Missing data at 3-month follow-up

    The percentage of missing in the dataset

    At 3-month follow-up

  • Missing data at 6-month follow-up

    The percentage of missing in the dataset

    At 6-month follow-up

  • Adverse events at baseline

    unfavorable and unintended events

    At baseline

  • Adverse events at 1-week follow-up

    unfavorable and unintended events

    At 1-week follow-up

  • Adverse events at 1-month follow-up

    unfavorable and unintended events

    At 1-month follow-up

  • Adverse events at 3-month follow-up

    unfavorable and unintended events

    At 3-month follow-up

  • Adverse events at 6-month follow-up

    unfavorable and unintended events

    At 6-month follow-up

Secondary Outcomes (3)

  • Chinese version of the Rosenberg Self-esteem Scale at 6-month follow-up

    At 6-month follow-up

  • Chinese version of the Pediatric Quality of Life Inventory at 6-month follow-up

    At 6-month follow-up

  • Chinese version of The Center for Epidemiologic Studies Depression Scale for Children at 6-month follow-up

    At 6-month follow-up

Study Arms (2)

Positive psychology

ACTIVE COMPARATOR

The experimental group(n=60), who will receive a 1.5-hour workshop covering positive psychology techniques delivered by a qualified research assistant, in groups of less than 5 people.

Behavioral: Positive Psychology

Control

NO INTERVENTION

The control group will receive no intervention.

Interventions

This intervention aim to examine the effectiveness of PPI in reducing depressive symptoms, enhancing self-esteem, and promoting quality of life among Chinese children who are living in poverty. Participants in the experimental group will receive a 1.5 hour workshop on 4 positive psychology techniques, including (1) gratitude visit/letters, (2) 3 good things, (3) you at your best, and (4) using signature strengths. A booster intervention will be given at 1-week follow-up.

Positive psychology

Eligibility Criteria

Age13 Years - 17 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Age from 13-17
  • Can read Chinese and speak Cantonese

You may not qualify if:

  • with identified cognitive and/or behavioral problem(s)
  • with identified mental problem(s)
  • participating in any mental health service/programme and/or receiving any psychiatric medication.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ka Yan Ho

Hong Kong, Hong Kong,China, 000, Hong Kong

RECRUITING

Related Publications (1)

  • Ho KY, Lam KKW, Bressington DT, Lin J, Mak YW, Wu C, Li WHC. Use of a positive psychology intervention (PPI) to promote the psychological well-being of children living in poverty: study protocol for a feasibility randomised controlled trial. BMJ Open. 2022 Aug 17;12(8):e055506. doi: 10.1136/bmjopen-2021-055506.

MeSH Terms

Conditions

Depression

Interventions

Psychology, Positive

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

PsychologyBehavioral SciencesBehavioral Disciplines and Activities

Study Officials

  • Eva Ho, PhD

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Katherine Lam, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 20, 2021

First Posted

May 6, 2021

Study Start

December 1, 2021

Primary Completion

August 30, 2023

Study Completion

August 30, 2023

Last Updated

April 19, 2022

Record last verified: 2022-04

Data Sharing

IPD Sharing
Will not share

Locations