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

H

Hong Kong University of Science and Technology

Status

Enrolling

Conditions

Mental Health Wellness
Healthy Diet

Treatments

Behavioral: T1: Mixed mode social support group
Behavioral: T2: Online mode social support group

Study type

Interventional

Funder types

Other

Identifiers

NCT05660837
HREP-2022-0170

Details and patient eligibility

About

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

Full 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.

Enrollment

400 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Filipino
  • Migrant domestic worker working in Hong Kong

Exclusion criteria

  • None

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

400 participants in 3 patient groups

T1: Mixed mode social support group
Experimental group
Description:
This group will receive programs in both online and off-line setting. There will be one face-to-face group session to get to know participant's peer group members. After the in-person group meeting, participants will meet in WhatsApp group. In WhatsApp group, facilitator will provide the following program
Treatment:
Behavioral: T1: Mixed mode social support group
Online social support group
Experimental group
Description:
This group will receive the same program as mixed mode social support group. The key differences would be delivery of all program components online.
Treatment:
Behavioral: T2: Online mode social support group
Control
No Intervention group
Description:
This is the control group. Control group will only participate in baseline and follow-up survey

Trial contacts and locations

1

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Central trial contact

Yaeeun Han

Data sourced from clinicaltrials.gov

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