NCT06418906

Brief Summary

This is an academic research study aiming to explore the relationships between equanimity, mindfulness, self-compassion, and mental health outcomes, and to examine the reliability and validity of the new measures in Hong Kong.

Trial Health

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Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2024

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2024

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

May 13, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 17, 2024

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
Last Updated

June 3, 2024

Status Verified

May 1, 2024

Enrollment Period

2 years

First QC Date

May 13, 2024

Last Update Submit

May 31, 2024

Conditions

Outcome Measures

Primary Outcomes (9)

  • Mindfulness (Five Facet Mindfulness Questionnaire - 20)

    The 20-item Five Facet Mindfulness Questionnaire - 20 (FFMQ-20) will be used to measure mindfulness. Possible score range is 20 to 100, where higher scores indicate higher mindfulness.

    2-week

  • Equanimity (Equanimity Scale)

    The 16-item Equanimity Scale (ES-16) will be used to measure equanimity. Possible score range is 16 to 80, where higher scores indicate higher equanimity.

    2-week

  • Self-compassion (Sussex-Oxford Compassion for the Self Scale)

    The 20-item Sussex-Oxford Compassion for the Self Scale (SOCS-S) will be used to measure self-compassion. Possible score range is 20 to 100, where higher scores indicate higher self-compassion.

    2-week

  • Depression (Patient Health Questionnaire - 9)

    The nine-item Patient Health Questionnaire - 9 (PHQ-9) will be used to measure depression. Possible score range is 0 to 27, where higher scores mean more severe depression.

    2-week

  • Anxiety (Generalized Anxiety Disorder - 7)

    The seven-item Generalized Anxiety Disorder-7 (GAD-7) will be used to measure anxiety. Possible score range is 0 to 21, where higher scores indicate more severe anxiety.

    2-week

  • Stress (Perceived Stress Scale - 10)

    The 10-item Perceived Stress Scale - 10 (PSS) will be used to measure stress. Possible score range is 0 to 40, where higher scores indicate higher perceived stress.

    2-week

  • Wellbeing (Short Warwick-Edinburgh Mental Wellbeing Scale)

    The seven-item Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS) will be used to measure wellbeing. Possible score range is 0 to 35, where higher scores mean higher mental wellbeing.

    2-week

  • Equanimity (Two-Factor Equanimity Scale)

    The Two-Factor Equanimity Scale (EQUA-S) will be used to measure equanimity, for assessing convergent validity of the ES-16. Possible score range is 14 to 70, where higher scores indicate higher equanimity.

    2-week

  • Self-compassion (Self-Compassion Scale - Short Form)

    The 12-item Self-Compassion Scale - Short Form (SCS-SF) will be used to measure self-compassion, for assess convergent validity of the SOCS-S. Possible score range is 12 to 60, where higher scores indicate higher self-compassion.

    2-week

Secondary Outcomes (1)

  • single-item measures on equanimity, mindfulness, self-compassion, depression, anxiety, stress (i.e., six items in total)

    2-week

Study Arms (1)

Community adults aged 18 or above

This is a single-arm study with no intervention involved. Adults aged 18 or above from the community will be invited to fill out the same set of questionnaires on a total of two time points: baseline and two-week post-baseline.

Other: Self-reported questionnaires

Interventions

After participants agree to participate in this study, they will first fill out the set of questionnaires once. After two weeks, the research team will send them reminders to fill out the same set of questionnaires again.

Community adults aged 18 or above

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Community participants aged 18 or above

You may qualify if:

  • aged 18 or above
  • can read and type Chinese
  • have means to access online surveys

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Psychology, The University of Hong Kong

Hong Kong, Hong Kong

RECRUITING

Study Officials

  • Hoi Chun Lok, MSocSc(CP)

    The University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Hoi Chun Lok, MSocSc(CP)

CONTACT

Amanda Kingsze Cheung, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 13, 2024

First Posted

May 17, 2024

Study Start

May 1, 2024

Primary Completion

May 1, 2026

Study Completion

May 1, 2026

Last Updated

June 3, 2024

Record last verified: 2024-05

Locations