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Coaching Intervention in Women At-risk of Common Mental Disorders

Coaching Intervention to Improve Mental Well-being of Community Women Who Are At-risk of Common Mental Disorders in Hong Kong: A Pilot Randomized Controlled Trials

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03751696
Enrollment
60
Registered
2018-11-23
Start date
2018-11-15
Completion date
2021-12-31
Last updated
2021-04-20

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

Conditions

Common Mental Disorder

Brief summary

This study aims to provide preventative intervention to 60 women who are at risk of common mental disorders in Hong Kong.

Detailed description

Participants will be recruited through the following routes: 1) by our partner non-governmental organizations, 2) by our research team through community outreach or training activities, 3) online screening tool, and 4) referral from organizations that provide service to women (e.g., Maternal and Child Health Clinics of Department of Health). Eligible subjects with informed consent provided will be randomly assigned to coaching group or SMS self-help tips. To test the effectiveness of the provided intervention programs, symptoms assessments and data collection on demographics and psychosocial data will be carried out during baseline, immediately, and 3 months post-intervention.

Interventions

BEHAVIORALGroup Coaching

4 sessions of 1-1.5-hour group coaching intervention within 8 weeks

BEHAVIORALSMS self-help tips

4 mental well-being tips through sms within 8 weeks

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Willing to provide written informed consent * Able to understand Cantonese and read/write Chinese * With subsyndromal or minor depressive symptoms indicated by * Depression subscale of Depression, Anxiety and Stress Scale (DASS) score 10-20 or * Edinburgh Postnatal Depression Scale (EPDS) scores 10-13

Exclusion criteria

* A positive response in items about suicidal thoughts if applicable (Yes, quite often and sometimes in EPDS) (These participants will be referred to suicidal management) * Those mental conditions that require other treatment priorities (e.g., suicidal risk, substance abuse, current or past episodes of psychotic disorder, personality disorders) * Those medical conditions that severely limit participation, comprehension, or adherence to treatment (e.g., epilepsy, dementia, terminal medical illness) * Those who are receiving structured psychotherapy or counseling

Design outcomes

Primary

MeasureTime frameDescription
Depressive symptomsimmediate post-interventionMeasured by the depression subscale of the Depression, Anxiety and Stress Scale
Anxiety symptomsimmediate post-interventionMeasured by the anxiety subscale of the Depression, Anxiety and Stress Scale

Secondary

MeasureTime frameDescription
Depressive symptoms3-month post interventionMeasured by the depression subscale of the Depression, Anxiety and Stress Scale (DASS). The subscale consists of 7 questions, each responses range from 0 (not applicable) to 3 (the most applicable). The higher score represents more severe depressive symptoms.
Anxiety symptoms3-month post interventionMeasured by the anxiety subscale of the Depression, Anxiety and Stress Scale

Countries

Hong Kong

Contacts

Primary ContactSuen YN, PhD
suenyn@hku.hk22554486
Backup ContactChan Yuk Yu
vinciyy@connect.hku.hk22554486

Outcome results

None listed

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