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临床试验/NCT06169943
NCT06169943尚未招募不适用

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

Chinese University of Hong Kong0 个研究点目标入组 80 人开始时间: 2024年9月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
80
主要终点
Physical activity level

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

盲法说明

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

入排标准

年龄范围
45 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

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

结局指标

主要结局

Physical activity level

时间窗: Baseline, 3, and 6 months

Total exercise amount will be quantified with a modified version of the Godin-Shephard Leisure-Time Physical Activity Questionnaire.

次要结局

  • Healthy eating(Baseline, 3, and 6 months)
  • Self-efficacy(Baseline, 3, and 6 months)
  • Waist circumference(Baseline, 3, and 6 months)
  • Body fat mass percentage(Baseline, 3, and 6 months)
  • Metabolic syndrome knowledge(Baseline, 3, and 6 months)
  • Perceived social support(Baseline, 3, and 6 months)
  • Blood pressure(Baseline, 3, and 6 months)
  • Body weight(Baseline, 3, and 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hon Lon Tam

Principal Investigator

Chinese University of Hong Kong

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