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Online Social Support Program for Physical and Mental Health of Filipino Migrant Domestic Workers in Hong Kong

Not Applicable
Recruiting
Conditions
Healthy Diet
Mental Health Wellness
Registration Number
NCT05660837
Lead Sponsor
Hong Kong University of Science and Technology
Brief Summary

The goal of this study is to test the effect of informational and emotional social support (via nutrition education, mental health support, and/or baking classes) through two different communication modalities (online vs. mixed mode / hybrid) on physical and mental health outcomes

Our research questions are the following.

1. Does an online social support program that provides informational and emotional support improve diet, anthropometry, and mental health?

2. Does a mixed-mode social support program that provides informational, emotional support through both online and face-to-face mode improve diet, anthropometry, and mental health?

3. Is a mixed mode social support program more effective in improving outcomes? Does meeting the group members face-to-face change the dynamics of online communication? If yes, what are the mechanisms? Are there differences in the following outcomes by communication modality?

1. Online bonding

2. Group identity

3. Quality of relationship

Detailed Description

Study design: Randomized controlled trial

1. Study description

Filipino Migrant Domestic workers (MDWs) working in Hong Kong will be eligible to apply. The investigators will advertise in Newspapers and Facebook commonly read by Filipino MDWs in Hong Kong. The investigators will recruit 400 MDWs over two phases and randomly assign them across three arms, T1) mixed-mode social support program; T2) Online social support program; and C) Control. Online social support program will be delivered through WhatsApp group chat. MDWs will self-fill surveys at Caritas office, but surveys will be assisted by survey enumerators as a group.

2. Logistics

Due to administrative constraints delivering interventions to 400 participants at the same time, the investigators will deliver interventions over two cohorts.

Cohort 1 (\~200 participants)

* Oct 31st-Dec 18th 2022 Baseline survey

* Jan 8th-March 18th 2023 Intervention (10 weeks)

* March 26th -April 16th 2023 Follow-up survey

Cohort 2 (\~200 participants)

* Feb 5th-March 19th 2023 Baseline survey

* March 20th-May 27th Intervention (10 weeks)

* May 28th - June 25th follow-up survey

Note 1: The investigators will enroll participants until the scheduled date for baseline survey or until the investigators recruit target sample size, whichever comes earlier.

Note 2: The investigators will keep the intervention design exactly the same for cohort 1 and cohort 2, and will not analyze data until data collection for both cohort 1 and cohort 2 is complete. Cohort 1 and cohort 2 will be analyzed as one sample.

3. Statistical analysis model - Estimation of treatment effect

In this section, the investigators outline the basic estimation approach to measuring the effect of the treatments on various outcomes.

Our basic treatment effects specification estimates the following equation:

y= β₀ + β₁T1 + β₂T2+ β₃X+ ε where y is the outcome of interest.

T1 and T2 are dummy variables equal to 1 if the participant was randomly assigned to the T1 and T2 group, respectively, and 0 otherwise. β₁ and β₂ represent the effect of being assigned to the specific treatment arm. X is a vector of baseline outcome and individual's characteristics including age, marital status, years working as migrant domestic workers, level of education, received food allowance. ε is an error term. The primary outcome variable, y, include nutrition knowledge, perceived social support, healthy diet, stress, anxiety, and depression. To compare the difference between T1 and T2, we will use F-test coefficient of equality.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
400
Inclusion Criteria
  • Filipino
  • Migrant domestic worker working in Hong Kong
Exclusion Criteria
  • None

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Nutrition knowledge score (change)Change from baseline nutrition knowledge at approximately 3-6 months.

Questions to test nutrition knowledge, survey questionnaire (score range 0-17, higher score means better outcome)

Stress (change)Change from baseline mental health at approximately 3-6 months.

Screen for stress using DASS-21 questionnaire, survey questionnaire (score range (0-42), higher score means worse outcome

Perceived social support (change)Change from baseline perceived social support at approximately 3-6 months.

Participant's perceived social support score, scale adapted from Oslo social support scale (OSSS-3), survey questionnaire, higher score means better outcome.

Healthy diet practices (change)Change from baseline diet practices at approximately 3-6 months.

Questions adapted from "starting the conversation (STC)" food frequency instrument, scale range 0-50, higher score means better outcome, survey questionnaire

Anxiety (change)Change from baseline mental health at approximately 3-6 months.

Screen for anxiety using DASS-21 questionnaire, survey questionnaire, score range (0-42), higher score means worse outcome

Depression (change)Change from baseline mental health at approximately 3-6 months.

Screen for depression using DASS-21 questionnaire, survey questionnaire, score range (0-42), higher score means worse outcome

Secondary Outcome Measures
NameTimeMethod
Peer pressuremeasured at end-line only (3-6 months after baseline survey)

10 questions: 5 point scale (strongly agree to strongly disagree), survey questionnaire

Body mass index (change)Change from baseline BMI at approximately 3-6 months.

kg/m2, anthropometry measurements

Waist-to-stature ratio (change)Change from baseline waist-to-stature ratio at approximately 3-6 months.

Waist circumference (cm)/Height (cm), anthropometry measurements

Waist-to-hip ratio (change)Change from baseline waist-to-hip ratio at approximately 3-6 months.

waist circumference (cm) /hip circumference (cm), anthropometry measurements

Online bondingmeasured at end-line only (3-6 months after baseline survey)

10 questions: 5 point scale (strongly agree to strongly disagree), survey questionnaire

Self-efficacy (change)Change from baseline self-efficacy at approximately 3-6 months.

four questions, General self-efficacy scale (GSE) survey questionnaire, score range 0-30, higher score means better outcome

Group identitymeasured at end-line only ( 3-6 months after baseline survey)

4 questions: 5 point scale (strongly agree to strongly disagree) , survey questionnaire

Trial Locations

Locations (1)

Hong Kong University of Science of Technology

🇭🇰

Hong Kong, Hong Kong

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