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Mhealth Social Support for People at Risk of Metabolic Syndrome

A Mhealth Social Support Program on Health Behaviors Among People at Risk of Metabolic Syndrome: a Feasibility Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06169943
Enrollment
80
Registered
2023-12-14
Start date
2024-09-30
Completion date
2025-05-31
Last updated
2024-08-14

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

Conditions

Metabolic Syndrome

Keywords

mhealth, metabolic syndrome, lifestyle modifications

Brief summary

This trial is to examine the feasibility, acceptability, and preliminary effect of a mHealth social support program on lifestyle modifications among people at risk of metabolic syndrome in Hong Kong at 3- and 6-month follow-ups.

Detailed description

Metabolic syndrome is a cluster of unhealthy conditions that affects more than 1 billion people in the world. Lifestyle modifications can reduce the risk to develop metabolic syndrome, while the report showed that over 95% of people in Hong Kong did not practice healthy lifestyle. This trial is to examine the feasibility, acceptability, and preliminary effect of a mHealth social support program on lifestyle modifications among people at risk of metabolic syndrome in Hong Kong. Eighty eligible participants will be recruited from community centers and be randomized into intervention group or control group. Participants in the control group will receive a mobile app with limited function, while those in the intervention group will receive a theory-guided mhealth social support program. Data will be collected at baseline, 3 months, and 6 months on the outcomes of feasibility, acceptability, and lifestyle modifications. Data will be analyzed using a generalized estimating equation based on the intention-to-treat principle. The findings of this study will provide valuable information for a full randomized controlled trial.

Interventions

OTHERmHealth social support program

This is a 3-month program comprises mobile app, group discussion, individual telephone contact, and reminders.

OTHERControl

The same mobile app as the intervention group but with limited function.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

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

Masking description

The outcome assessor will be blinded to the participants' group allocation throughout the study.

Intervention model description

Intervention group Control group

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Chinese adults aged ≥ 45 years 2. With central obesity according to IDF criteria 3. Being treated of hypertension, dyslipidemia, or diabetes 4. Able to give informed consent 5. Attain at least 6 years of formal education 6. Have a smartphone with internet connection and able to use WhatsApp

Exclusion criteria

1. Concurrently participating in another clinical trial, lifestyle/dietary intervention, or weight control program 2. Known history of psychiatric disorders

Design outcomes

Primary

MeasureTime frameDescription
Physical activity levelBaseline, 3, and 6 monthsTotal exercise amount will be quantified with a modified version of the Godin-Shephard Leisure-Time Physical Activity Questionnaire.

Secondary

MeasureTime frameDescription
Metabolic syndrome knowledgeBaseline, 3, and 6 monthsChinese version of metabolic syndrome knowledge scale. 10 items cover three domains: definition and diagnosis (5 items), complications (2 items), and preventions (3 items); a higher sum score indicates better understanding of metabolic syndrome.
Perceived social supportBaseline, 3, and 6 monthsChinese version of multidimensional scale of perceived social support. 12 items measuring perceived support from family and friends; 7-point Likert scale (1=strongly disagree to 7=strongly agree), ranged from 12 -84; a higher sum score indicates more social support is perceived.
Self-efficacyBaseline, 3, and 6 monthsNutrition and Exercise subscale of the Chinese version of Self-rated Abilities for Health Practices. 7 items measuring diet self-efficacy and 7 items measuring PA self-efficacy; five-point Likert scale (0=not confident to 4=very confident) that a higher score indicates higher confidence to adopt lifestyle modifications in daily life.
Healthy eatingBaseline, 3, and 6 monthsDiet subscale of the Chinese version of Health Promoting Lifestyle Profile II. The subscale includes eight items measuring healthy eating on a 4-point Likert scale (1=never to 4=routinely), ranged from 8-32. The higher sum score indicates more adoption of healthy eating.
Waist circumferenceBaseline, 3, and 6 monthsMeasured in the nearest 0.1 centimeter.
Body weightBaseline, 3, and 6 monthsMeasured in the nearest 0.1 kilogram.
Body fat mass percentageBaseline, 3, and 6 monthsBody fat mass percentage will be assessed by a calibrated digital body composition monitor.
Blood pressureBaseline, 3, and 6 monthsBoth systolic blood pressure and diastolic blood pressure will be measured by a validated and reliable upper-arm automated system (in mmHg) after resting for 20 minutes; an average of two measurements with 1-minute apart is recorded.

Outcome results

None listed

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