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A Brief Body-mind-spirit Intervention to Promote Positive Emotions

A Brief Body-mind-spirit Intervention to Promote Positive Emotions - a Pilot Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04582526
Enrollment
120
Registered
2020-10-09
Start date
2020-11-30
Completion date
2023-01-31
Last updated
2020-11-05

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

Conditions

Emotions, Stress

Keywords

Personal well-being, Family well-being

Brief summary

Integrating ICT in health promotion has been suggested to offer many advantages compared to traditional approaches to promote well-being. Research has shown the positive effects of a body-mind-spirit (BMS) approach in enhancing health and well-being. We will develop and assess a pilot trial involving a holistic BMS approach to promote positive emotion change, emotion regulation and self-awareness through an ICT-supported program in a community setting.

Detailed description

The body-mind-spirit (BMS) approach views the three components as a connected, balanced system that interacts with one another harmoniously. With the well-established academic-community partnership between HKU and Caritas-Hong Kong, our pilot trial aims to build upon the previous experiences by Caritas-Hong Kong and investigate the feasibility and effectiveness of a BMS approach in enhancing positive emotions and well-being among community participants. This trial is an innovative attempt at conducting an ICT-supported online intervention with community participants. It would also help meet the urgent need for brief, community-based preventive mental health promotion, especially in the context of the COVID-19 pandemic.

Interventions

BEHAVIORALBMS program

A BMS program with three components: relaxation exercises, healthy eating, expressive arts therapy

Sponsors

Caritas Medical Centre, Hong Kong
CollaboratorOTHER
The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Chinese-speaking; * Individuals aged 18 years and above; * No history of diagnosed mental illness; * Access to an internet-connected computer.

Exclusion criteria

* Individuals who cannot meet the inclusion criteria.

Design outcomes

Primary

MeasureTime frameDescription
Positive emotionBaseline and one monthChange assessed by the Subjective Happiness Scale (SHS). The minimum and maximum of SHS are 4 to 24, respectively. A higher score means a better outcome.

Secondary

MeasureTime frameDescription
Personal well-beingBaseline and one monthChange assessed by a one-item Personal Happiness scale. The minimum and maximum of SHS are 0 to 10, respectively. A higher score means a better outcome.
Family well-beingBaseline and one monthChange assessed by a 3-item Family well-being scale. The minimum and maximum are 0 to 30, respectively. A higher score means a better outcome.
Negative emotionBaseline and one monthChange assessed by the Patient Health Questionnaire-4. The minimum and maximum of SHS are 0 to 28, respectively. A higher score means a worse outcome.
Stress levelBaseline and one monthChange assessed by the Perceived Stress Scale (PSS). The minimum and maximum of SHS are 0 to 16, respectively. A higher score means a worse outcome.
Knowledge and attitudes towards and practice of the holistic BMS health care approachBaseline and one monthChange assessed by outcome-based questions. A score of each question ranges from 1-5. A higher score a better outcome.
Perceived benefits of the BMS programOne monthAssessed by outcome-based questions with categorical choices
Sharing of BMS with othersOne monthAssessed by outcome-based questions with categorical choices
Sleep qualityBaseline and one monthChange assessed by the Insomnia Severity Index (ISI). The minimum and maximum of SHS are 0 to 28, respectively. A higher score means a worse outcome.

Contacts

Backup ContactTai-hing Lam, MD
hrmrlth@hku.hk39179287
Primary ContactAgnes Y Lai, PhD
agneslai@hku.hk39176779

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026